Management Options for Advanced Low or Intermediate Grade Gastroenteropancreatic Neuroendocrine Tumors: Review of Recent Literature

Neychev, Vladimir; Kebebew, Electron

doi:https://doi.org/10.1155/2017/6424812

International Journal of Surgical Oncology

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Review Article | Open Access

Volume 2017 | Article ID 6424812 | https://doi.org/10.1155/2017/6424812

Management Options for Advanced Low or Intermediate Grade Gastroenteropancreatic Neuroendocrine Tumors: Review of Recent Literature

Vladimir Neychev^1,2and Electron Kebebew²

Academic Editor: Theodore D. Liakakos

Received30 Jan 2017

Revised13 Apr 2017

Accepted26 Apr 2017

Published16 May 2017

Abstract

Our understanding of the biology, genetics, and natural history of neuroendocrine tumors (NETs) of the gastrointestinal tract and pancreas has improved considerably in the last several decades and the spectrum of available therapeutic options is rapidly expanding. The management of patients with metastatic low or intermediate grade NETs has been revolutionized by the development of new treatment strategies such as molecular targeting therapies with everolimus and sunitinib, somatostatin analogs, tryptophan hydroxylase inhibitors, and peptide receptor radionuclide therapy that can be used alone or as a multimodal approach with or without surgery. To further define and clarify the utility, appropriateness, and the sequence of the growing list of available therapies for this patient population will require more high level evidence; however, data from well-designed randomized phase III clinical trials is rapidly accumulating that will further stimulate development of new management strategies. It is therefore important to thoroughly review emerging evidence and report major findings in frequent updates, which will expand our knowledge and contribute to a better understanding, characterization, and management of advanced NETs.

1. Introduction

Neuroendocrine tumors (NETs) of the gastrointestinal tract and pancreas are rare and heterogeneous, but clinically important group of neoplasms with unique tumor biology, natural history, and clinical management issues [1, 2]. NETs develop from the dispersed neuroendocrine cells of the gastrointestinal tract (GI) mucosa (also called “carcinoids”) and the pancreatic islet cells. Approximately 85% of NETs are sporadic and the remainder occur as part of familial cancer syndromes including multiple endocrine neoplasia-type 1 (MEN1), von Hippel-Lindau disease (VHL), von Recklinghausen’s disease (neurofibromatosis 1, NF1), and tuberous sclerosis (TS) [3–5].

Neuroendocrine cells are one of the largest groups of hormone-producing cells in the body. At least 13 distinct gut neuroendocrine cells exist, all of which may develop tumors and/or oversecrete various bioactive peptides or amines including serotonin, somatostatin, histamine, and gastrin. Hypersecretion of these hormones can result in significant morbidity and mortality. Up to 20% of patients with NETs may develop carcinoid syndrome: flushing, abdominal pain, diarrhea, bronchoconstriction, and carcinoid heart disease [6].

Treatment of NETs is largely dependent on the functional status and the stage. Advanced NETs are characterized by local invasion and regional and distant metastases. While the treatment of localized NETs is surgical resection, a variety of therapeutic options are available for patients with advanced NETs. These include medical control of excess hormone levels and associated symptoms, cytoreductive surgery for patients with advanced disease, radioembolization, chemoembolization, systemic chemotherapy, interferon, long-acting somatostatin analogs, and peptide receptor-targeted radionuclide therapy. When to utilize a given option, what combination therapeutic approach should be used, how long treatment should be continued, and in what subgroup of patients should a particular treatment option be used are a work in progress.

2. Classification, Epidemiology, and Prognosis

The annual incidence of NETs has been increasing worldwide [1, 5, 7, 8]. Whereas early studies have reported incidence rates of <1 per 100,000 persons per year, recent age-adjusted epidemiologic studies have shown a significant, more than fivefold, increase in NETs incidence from 1973 to 2005 [5, 7, 8]. Based on data from the National Cancer Institute’s Surveillance, Epidemiology and End Results (SEER) cancer registry database, the annual incidence of NETs was estimated to be 7.8 per 100,000 persons in 2013 [5]. The prevalence of NETs has been estimated as 35 per 100,000 and may be considerably higher if clinically “silent” tumors are included [9].

A population-based study conducted in Canada showed that the incidence of NETs has markedly increased over the course of 15 years from 2.48 cases per 100,000 people per year in 1994 to 5.86 per 100,000 per year in 2009 [10]. Outside USA, Canada, and Europe, epidemiological surveys have been conducted in Japan showing that the number of treated patients with NETs in 2010 increased approximately 1.2-fold compared to 2005 and the number of new incidences of NETs in 2010 was nearly 2-fold greater than in 2005 [11].

NETs are generally classified into functioning (hormone hypersecreting) or nonfunctioning (clinically “silent”) tumors, based on their ability to produce hormone-associated symptoms [12]. However, other classification systems with many common themes, such as the distinction of well-differentiated (low and intermediate grade) from poorly differentiated (high-grade) NETs and the tumor proliferative index, have been used over the past 5 decades (Table 1). In general, well-differentiated, low or intermediate grade NETs have a relatively indolent behavior with slow progression but poorly differentiated tumors may exhibit highly aggressive behavior with rapid metastatic spread that is clinically indistinguishable from pancreatic adenocarcinoma or small-cell lung cancer [3]. Fortunately, poorly differentiated tumors account for only a small subset of all NETs.

Recent large, epidemiologic studies have shown that majority of NETs (60–90%) are clinically nonfunctioning, well-differentiated, slow-growing neoplasms diagnosed, in most instances, incidentally during unrelated procedures or diagnostic tests [1, 4, 6, 13]. As a result of this insidious biological behavior, many patients with NETs have advanced disease at diagnosis, with regional or distant metastasis observed in up to 80% of patients [7, 13].

Even though there has been a significant improvement in the diagnosis and management of NETs, no significant change in survival has been observed over the last 30 years [4, 5]. Reported survival times for patients with advanced NETs in population-based and institutional series are highly variable likely due to differences in tumor biology, classification, treatment modalities, and patient selection. According to data from the SEER database, the median overall survival (OS) for patients with metastatic NETs was two years [7], whereas, in a large institutional database, the median OS for a similar group of patients was 5.8 years [14]. According to the European Neuroendocrine Tumor Society (ENETS) consensus statement, the median OS of nonfunctional NETs was 38 months with a 5-year survival rate of 43% [15].

3. Management of Advanced NETs

Currently available therapeutic options for patients with NETs can be summarized and subdivided into four major categories: () locoregional therapeutic options, including surgical resection or liver-directed therapies such as radiofrequency ablation (RFA), transcatheter arterial hepatic embolization (TAE), transcatheter arterial hepatic chemoembolization (TACE), or radioembolization therapy (TARE), () somatostatin receptor targeting therapeutic options, including somatostatin analogs and peptide receptor radionuclide therapy (PRRT), and tryptophan hydroxylase inhibitors, () molecular and mutation targeting therapy, and () systemic chemotherapy.

4. Locoregional Therapeutic Options

4.1. Surgical Resection

Surgical resection is the mainstay of treatment for patients with early-stage disease; however, the extent, timing, and effect of surgical intervention for advanced, metastatic NETs remain controversial. NETs most commonly metastasize to the locoregional lymph nodes and liver and 25% to 93% of patients will develop liver metastases [16]. Prospective randomized data on the treatment of liver metastases of NETs are lacking and there is considerable debate regarding the optimal surgical management [17–20]. Despite the lack of randomized control data, the current concept for the surgical treatment of patients with advanced NETs is that, when feasible, aggressive surgical resection is associated with the best symptom-free and long-term survival results [4, 16, 20, 21]. More specifically, the ENETS revised consensus statement emphasized that resection should be the first-line treatment option for patients with advanced NETs if 90% or more of the disease burden can safely be resected [22]. However, only 5% to 20% of patients with advanced NETs meet this “conventional” criterion and there is no evidence from randomized studies in the literature for the role of cytoreductive surgery in unresectable metastatic NETs [23].

4.2. Role of Aggressive Surgical Resection

A number of retrospective and small prospective studies, summarized previously in several elegant systematic reviews, have analyzed the potential role of surgery for advanced metastatic NETs [24–29].

Some have shown that resection of primary tumor and liver metastases in patients with advanced pancreatic NETs () resulted in an overall survival (OS) of 71% (median: 76 months) and progression-free survival (PFS) of 5% (median: 21 months) at 5 years [31]. Others reported that resection of the primary tumors and liver metastases in 170 patients (108 functional tumors) resulted in OS of 61% and 35% at 5 and 10 years, respectively, without differences between GI and pancreatic NETs or functional and nonfunctional tumors [32]. Recurrence rate of complete () versus incomplete () resection was 76% and 91% at 5 years (median time to recurrence 30 months versus 16 months, resp., ). Symptoms relief was achieved in 104 of 108 patients (96%), but the recurrence rate of symptoms was 59% [32]. A retrospective study of 54 patients with advanced metastatic NETs (30% functional tumors) has shown that patients with resection of primary tumor site only () had better survival than patients without surgery at all () (60% versus 30% at 5 years, resp.; ) [33].

The impact of aggressive surgical resection on performance status and symptoms control was evaluated in symptomatic patients () with advanced GI NETs and an extensive liver involvement [34]. All patients had surgical exploration during which some patients () had an adjunct RFA of one or more liver lesions. Postoperatively, 5-hydroxyindoleacetic acid (HIAA) decreased by 50% in all patients with symptomatic improvement reported in 25 patients (83%). Mean pre- and postoperative Karnofsky physical performance scores were 55 and 85, respectively () [34].

Analysis of records from an international database of eight major hepatobiliary centers including 339 patients with metastatic NETs demonstrated that aggressive surgery resulted in OS of 74% and 51%, at 5 and 10 years, respectively; however, disease recurred in 94% of patients at 5 years. Patients with hormonally functional NETs who had / resection benefited the most from surgery () [35].

Assessment of the impact of surgical () versus medical () treatment on quality of life (QoL) of patients with advanced metastatic NETs and symptoms of hormonal overproduction showed that less than one-fourth of patients experienced a significant improvement in QoL after treatment [36]. There was no difference in the improvement in overall QoL in respect to treatment modality; however, a lower proportion of patients were dissatisfied with surgery versus nonsurgical therapy (5.4% versus 9.4%, ) [36].

A retrospective study evaluated the efficacy of multimodal hepatic cytoreduction including resection, radiofrequency ablation, chemoembolization, or combined therapy in 15 symptomatic patients with advanced hepatic metastases from GI NETs. At a mean follow-up of 29 months, 6 patients (40%) had stable disease, 8 (53.3%) had progression of disease, and 1 (6.6%) had no evidence of disease. The median symptom relief period was 12 months and OS was 57 months (mean) [37].

Another study of 41 patients with an extensive hepatic resection for NETs with liver-localized metastases and median follow-up of 51 months (range: 7 to 165) showed that recurrences developed in 32 patients (78%) mainly in the liver after a median of 19 months (range: 2 to 79) [38]. Five-year OS and disease-free survival (DFS) rates were 79% and 3%, respectively [38]. Another such study investigated the effect of the resection of liver metastases in 172 patients with advanced NETs and revealed that surgery resulted in a median OS of 9.6 years (range: 89 days to 22 years) [39].

A similar analysis of records of 72 patients with curative () or palliative () resection of pancreatic NETs with hepatic metastases revealed an OS at 1, 5, and 10 years of 97%, 60%, and 45%, respectively [40]. Among the patients with a complete () resection, the 1- and 5-year disease-free survival were 53.7% and 10.7%, respectively. For patients undergoing debulking of 90% tumor burden, the 1- and 5-year survival free of progression were 58.1% and 3.5%, respectively [40]. Another single-center study of 204 patients with hepatic NET metastases showed that patients with an resection () had an excellent OS of 90.4% at 10 years, while () or () resection had a 10-year survival of 53.4 and 51.4%, respectively [41]. The majority of the patients (53.9%) were not surgical candidates and had a poor 10-year survival rate of 19.4%. Partial or complete control of endocrine-related symptoms was achieved in all patients with functioning tumors following surgery [41].

A prospective study evaluated outcomes from a complete cytoreductive surgery of peritoneal metastases in 41 patients with advanced NETs with () or without () hyperthermic intraperitoneal chemotherapy (HIPC) [42]. Sixty-six percent of these patients also had resection of liver metastases during the same procedure. OS was 69% and 52%, and DFS was 17% and 6% at 5 and 10 years, respectively. While the OS was not impacted by the performance of HIPC, DFS was greater in the HIPC group (66%) when compared to patients without HIPC (47%), at 5-year follow-up () [42].

A recent study reported outcomes of curative liver resection for advanced NETs in 376 patients [43]. The median and 5-year DFS were 4.5 years and 46%, respectively. The probability of being cured by liver surgery was 44% with time to cure of 5.1 years. A multivariable cure model found type and grade of NETs, as well as rate of liver involvement, to be independent predictors of cure. The cure fraction for patients with well-differentiated GI NETs or functional pancreatic NETs and liver involvement < 50% was 95%, while the presence of all the three unfavorable prognostic factors (nonfunctional pancreatic NET, liver involvement > 50%, and moderate/poor differentiation) rendered cure fraction of 8% [43]. Another recent large-cohort study of 800 patients with cytoreductive surgery for advanced NETs showed a median OS for patients with pancreatic NETs of 124 months (5-, 10-, and 20-year OS rates were 67%, 51%, and 36%, resp.) [44]. Median OS for patients with GI NETs was 161 months (5-, 10-, and 20-year OS rates were 84%, 67%, and 31%, resp.) [44].

4.3. Role of Liver Transplantation

The potential role of liver transplantation in management of patients with advanced NETs remains controversial and although it is not generally recommended, the available data suggest that it may be an option in highly selected patients with well-differentiated, functional NETs with extended liver metastases refractory to multiple systemic treatments and excluded extrahepatic disease by optimized staging [27, 45, 46]. Some series have reported promising outcomes in well-selected patients after liver transplantation with an OS of 70 to 73% at 5 years from diagnosis of liver metastases [47, 48]. Others have reported less favorable results, with a posttransplant 5-year survival rate as low as 49% to 58% in transplant recipients [49, 50].

In summary, despite the lack of large randomized control studies, there is a growing body of evidence from an increasing number of retrospective and prospective studies showing that surgical resection of advanced metastatic NETs with curative intent or for palliation provides favorable oncological outcomes with significant alleviation of symptoms and improvement of survival. While most studies make it clear that the aim of surgery should be status, the role of surgical debulking () in patients where an resection cannot be achieved remains debatable. It has been shown by some that selected patients may benefit from or resection especially for symptoms control and that there may be a potential benefit from resection of the primary lesion only in patients with otherwise unresectable liver metastases [26]. On the other hand, others have shown less favorable results with no evidence to support the use of a resection to improve either OS or QoL in patients with advanced metastatic NETs [25].

Despite exhaustive surgery hepatic or extrahepatic recurrences are frequent and may develop early [24–29]. Thus, it is becoming increasingly clear that new, perhaps combination (surgical and medical) therapeutic strategies to improve the outcomes of patients with advanced NETs need to be explored [51].

4.4. Minimally Invasive, Liver-Directed Therapy

Due to the insidious behavior of NETs and indolent course of the disease, many patients will present with liver metastases, which is associated with a poor prognosis [52]. In contrast to normal hepatic parenchyma that depends largely on portal venous circulation, the hypervascular liver NETs metastases rely primarily on hepatic artery blood supply. Thus, during the tumor ischemia produced by TAE liver-directed therapy, normal liver tissue will be relatively protected. Compared with systemic chemotherapy or radiation, TACE and TARE combining delivery of radio or chemotherapeutics with embolization of tumor arterial blood supply offer several advantages, including significantly increased local, peritumoral drug or radioactivity concentration and local cytotoxic effects with decreased systemic toxicities [53]. Various chemotherapeutic agents including doxorubicin, streptozocin, cisplatin, 5-fluorouracil, and mitomycin-C alone or in combination as well as beta-emitting radioactive agents such as 90Yttrium have been used for TACE and TARE; however, there is no consensus on which therapeutic agent to use, and it remains unclear if TACE and TARE offer outcome advantage over bland embolization for this patient population [52, 54]. In addition, no significant difference in safety profiles of these liver-directed modalities was found with the most common adverse events being nausea, vomiting, abdominal pain, and fever [52]. Although the number of studies investigating RFA treatment of NET liver metastases is limited, percutaneous or laparoscopic use of RFA alone or in combination with surgery has been shown to be effective in both relieving symptoms and achieving local control of NET liver metastases [22].

None of the liver-directed techniques has been shown to be more beneficial than the others and histological proof of the complete destruction of tumor foci is difficult to obtain; however, these minimally invasive therapies are showing increasingly favorable results including increased progression-free survival (PFS) and OS rates and improved symptomatic response [55].

A prospective multicenter phase II study evaluated safety and dose reproducibility of 90Yttrium TARE in the treatment of patients with diverse liver metastases, including a relatively large cohort of patients with NETs () [56]. For patients with advanced NETs, disease control rate at 1 year was 93% and median PFS and medium survival were not achieved [56]. A meta-analysis of studies with 90Yttrium TARE in patients with metastatic NETs demonstrated an objective response rate (OR) of 50% and disease control rate of 86% [57].

Another recent systematic review analyzing benefits and risks of hepatic resection versus nonsurgical treatments in patients with resectable liver metastases showed no robust evidence that a liver resection was superior to any other liver-directed therapies including TAE, TACE, TARE, and RFA in improving OS, PFS, or QoL [25].

More recently, a large prospective study evaluated outcomes of hepatic resection, RFA, TACE, systemic therapy, or observation as separate or combined procedures in 649 patients with advanced NETs metastatic to the liver [44]. Median and 5- and 10-year OS for each treatment group were as follows: patients with hepatic resection (), 160 months, 90%, and 70%, respectively; RFA (), 123 months, 84%, and 55%, respectively; TACE (), 66 months, 55%, and 28%, respectively; systemic therapy (), 70 months, 58%, and 31%, respectively; and observation (), 38 months, 38%, and 20% [44].

5. Somatostatin Analogs, Tryptophan Hydroxylase Inhibitors, and Somatostatin Receptor Targeting Therapy

5.1. Somatostatin Analogs Therapy

A unique feature of most NETs is the expression of somatostatin receptors (SR) by the tumor cells. There are five different SR subtypes and more than 80% of NETs express multiple subtypes, with a predominance of receptor subtypes 2 and 5 [13]. Somatostatin is an endogenous SR agonist which inhibits the secretion of a broad range of hormones from the endocrine system, including serotonin, insulin, glucagon, vasoactive intestinal peptide, and gastrin [58]. Somatostatin has limited clinical use due to its short half-life (<3 min); however, somatostatin analogs (SA) such as octreotide, lanreotide, and pasireotide and their long-acting release formulations (LAR) play an important role in the treatment of patients with NETs [59–61]. With the exception of insulinoma that is less responsive to SA due to lower expression of SR and gastrinoma treated initially with proton pump inhibitors, SA are generally considered the first-line treatment for patients with functional NETs and symptoms of hormonal hypersecretion [62–64]. Although SA are mainly used to treat symptoms of hormone hypersecretion, there is emerging evidence from several ongoing or completed clinical trials suggesting that SA have antiproliferative activity (Table 2).

A phase III, randomized, placebo-controlled study (PROMID trial) demonstrated prolonged PFS (14.3 versus 6.0 months in the placebo arm) in patients with well-differentiated small bowel NETs and low hepatic tumor volume treated with octreotide LAR [65]. The most frequently observed severe adverse events, regardless of causal relationship to treatment, were observed more often in the octreotide LAR arm and included diarrhea and flatulence [65]. A follow-up PROMID study tested the effect of octreotide LAR on OS and found patients assigned to octreotide and placebo had only slightly different OS, 84.7 versus 83.7 months, respectively () [66].

Additionally, a recent phase III, randomized, double-blind, controlled study (CLARINET trial) reported that extended-release aqueous-gel formulation of lanreotide has an antitumor effect against a broader spectrum of nonfunctional enteropancreatic NETs with significantly improved PFS (median not reached versus 18.0 months in the placebo arm) [62]. The most common treatment-related adverse event was diarrhea (26% of the patients in the lanreotide group and 9% in the placebo group) [62]. The expanding role of SA in the treatment of NETs beyond their symptom controlling properties has been further elegantly outlined in several recent reviews [63, 67, 68].

Although octreotide and lanreotide have been shown to be increasingly useful for the treatment of advanced NETs, drug resistance or escape phenomenon has been reported to possibly account for the decreased efficacy of the drugs after 6 to 18 months of therapy [13, 68]. A phase II, open-label, multicenter study of pasireotide, an SA with high affinity for SR types 1, 2, 3, and 5, showed that this drug was effective in 27% of patients with advanced NETs whose symptoms (diarrhea/flushing) were inadequately controlled by octreotide LAR [69]. The most common, mild or moderate severity drug-related adverse events were nausea (27%), abdominal pain (20%), weight loss (20%), and hyperglycemia (16%). Another phase II clinical trial evaluating the antiproliferative activity of pasireotide in treatment-naive patients with advanced NETs showed a median PFS of 11 months with the most favorable effect observed in patients with low hepatic tumor burden, normal baseline chromogranin A, and high expression of SR type 5 in tumor cells [70]. The most common adverse effect observed was hyperglycemia in 79% of patients [70].

5.2. Tryptophan Hydroxylase Inhibitors

Somatostatin analogs alone or in combination with surgery, radiation, or embolization have been successfully used for control of symptoms in patients with advanced NETs who develop carcinoid syndrome. Yet, a significant proportion of these patients remain refractory to treatment with SA and suffer from debilitating symptoms of serotonin overproduction [75]. Telotristat etiprate (TE) is a novel oral inhibitor of tryptophan hydroxylase, the rate-limiting enzyme for conversion of tryptophan to serotonin, that showed promising efficacy and safety profiles in several phase I and phase II trials conducted in the USA and Europe [76, 77]. The primary outcomes in the phase II clinical trials were (1) biochemical response (at least 50% reduction or normalization in urinary excretion of serotonin breakdown product HIAA) and (2) clinical response defined as a reduction in the daily mean number of bowel movement of at least 30% from baseline or normalization in the daily mean number per week (achievement of a daily mean ≤ 3 bowel movements per week). The results of these studies were consistent and showed a significant reduction in bowel movement frequency (with patient reported improvement of QoL) and a sustained, significant decrease in urinary HIAA. These early clinical studies supported the conduct of a placebo-controlled, double-blind, phase III clinical trial (TELESTAR) of 211 patients with carcinoid syndrome randomly assigned to placebo () or TE 250 mg () or TE 500 mg (), each given 3 times per day for 12 weeks [75, 78]. Patients who qualified for TELESTAR were on stable-dose SA therapy at enrolment, continued SA therapy throughout study period, and had ≥4 bowel movements per day. TELESTAR was accompanied by a satellite study (TELECAST) with the same randomization design that included patients who did not qualify for TELESTAR, because they had <4 bowel movements per day or do not tolerate or will not take SA. Median bowel movement frequency was 5.7 per day (TELESTAR) and 2.5 per day (TELECAST), and mean urinary HIAA was 84 mg/24 hours. The results of TELESTAR study showed that compared to the placebo group () patients taking 250 mg () and 500 mg () TE experienced a median reduction of 0.81 () and 0.69 () bowel movements daily, respectively. There was a significant and durable reduction in absolute mean urinary HIAA from baseline of patients on 250 mg () and 500 mg () TE with 40.13 mg/24 hours and 57.73 mg/24 hours, respectively, compared to placebo group () that showed an increase with 11.47 mg/24 hours (). Integrated safety analyses showed no serious adverse effects with slightly higher rates of nausea, constipation, and depression reported with TE.

In summary, TE has the potential to reduce serotonin levels and become a valuable alternative for the treatment of patients with advanced NETs and carcinoid syndrome refractory to treatment with SA.

5.3. Peptide Receptor Radiotherapy (PRRT)

The potential therapeutic benefits of nuclear medicine using radiolabeled SA are of great practical research interest and are currently being used in multiple European medical centers for the treatment of patients with NETs [79]. PRRT is based on the principle used in 111Indium-labeled octreotide scintigraphy and 68Gallium-labeled DOTA PET/CT but utilizes SA radiolabeled with β-emitters such as 177Lutetium-DOTATATE (177Lu-DOTATATE) and 90Yttrium-DOTATOC (90Y-DOTATOC). Such an approach has been shown as an effective treatment option in patients with advanced, metastatic NETs in multiple phase I and II clinical trials (Table 3) [64, 80–82].

One large retrospective study of more than 500 patients with advanced NETs treated with 177Lu-DOTATATE showed complete or partial response (PR) in 30% and minor response in 16% of the patients [80]. The most commonly reported acute (within 24 hours) toxicities included nausea, vomiting, and abdominal pain; subacute hematologic toxicity (4 to 8 weeks after administration) occurred in 9.5% of patients and alopecia in 62%. Nine patients experienced serious delayed toxicities, including renal insufficiency (), liver toxicity (), and myelodysplastic syndrome () [80]. The therapeutic effect of 90Y-DOTATOC has been evaluated in several phase I and II clinical trials that showed modest response rates, ranging from 25% to 30% with renal toxicity being the most common dose-limiting adverse event (Table 3) [91, 92].

Although the majority of available results of PRRT benefits are from retrospective studies or phase I and II trials, the first phase III, randomized, multinational clinical trial of PRRT comparing therapeutic effect of 177Lu-DOTATATE (Lutathera®) to high dose octreotide LAR (NETTER-1 study) has been recently completed with promising findings [83, 93, 94]. Patients with inoperable, grade 1 or 2, progressive, somatostatin receptor positive midgut NETs were randomized (1 : 1) to receive Lutathera () every 8 weeks (administered 4 times) versus octreotide LAR 60 mg () every 4 weeks. The primary endpoint was PFS and the secondary endpoints included objective response rate (OR), OS, time to progression (TTP), safety, tolerability, and health-related QoL. At the time of statistical analysis, the median PFS was not reached for Lutathera group and was 8.4 months with 60 mg octreotide (). Altogether, 23 confirmed disease progressions or deaths were observed in the Lutathera group versus 67 in the octreotide LAR group. The safety profile was consistent with the safety information generated in the phase I-II clinical trials reviewed above [94]. As a result of this phase III trial that provided strong evidence for a clinically meaningful benefit for patients with advanced NETs treated with Lutathera, this novel compound has received orphan drug designation from the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA).

6. Molecular and Mutation Targeted Therapy

Our knowledge of the genetic alterations present in sporadic and familial NETs has improved significantly. Mutations in driver oncogene and tumor suppressor genes have been identified in most NETs [71, 72, 95]. Overexpression of growth factors and their receptor such as vascular endothelial growth factor (VEGF), VEGF receptor (VEGFR), platelet-derived growth factor (PDGF), and PDGF receptor (PDGFR) [96] and/or somatic mutations in MEN1, DAX, ATRX, and TP53 and the genes of mammalian target of rapamycin (mTOR) signaling pathway are common in NETs [7, 97].

6.1. Everolimus: Targeting Altered mTOR Pathway

Several studies, using whole-exome-sequencing approach and expression profiling, have consistently identified somatic mutations in and or activation of the PI3K/AKT/mTOR pathway as a common event in NETs [96, 97]. The mTOR pathway has a central role in cancer cell growth, proliferation, differentiation, and apoptosis. Tuberous sclerosis 2 (TSC2), phosphatase and tensin homolog (PTEN), PIK3CA, and fibroblast growth factor 13 (FGF13) are among the key modulators of the mTOR pathway [98, 99]. Several studies of global gene expression profiling in a large panel of pancreatic NETs showed that TSC2 gene and PTEN gene were downregulated in most tumors, and their low expression was significantly associated with shorter disease-free survival and OS [100]. In addition, high FGF13 expression level was significantly associated with liver metastasis and shorter disease-free survival [100]. A recent whole-exome sequencing study also revealed the presence of somatic mutations in MEN1, DAXX, ATRX, TSC2, PTEN, and PIK3CA genes in the majority of sporadic NETs [97]. Furthermore, patients with NETs harboring these somatic mutations had a longer survival when compared to patients with wild type MEN1 and/or DAXX/ATRX [97].

Activation of the mTOR pathway has also been implicated in several familial cancer syndromes (tuberous sclerosis (TS), neurofibromatosis type 1 (NF1), and Hippel-Lindau diseases (VHL)) associated with the development of NETs [101, 102]. Findings of these and other studies further support the critical role of the mTOR pathway in NETs and add to the wealth of data that has spurred the clinical development of mTOR inhibitors as a treatment option for patients with advanced NETs (Table 2).

Everolimus is a well-studied oral mTOR inhibitor. A phase II trial of everolimus in combination with long-acting octreotide in patients with advanced low to intermediate grade NETs (30 carcinoid and 30 islet cell tumors) demonstrated a partial response rate of 20% and median PFS of 15 months [103, 104]. A follow-up phase II trial, which randomized patients with metastatic pancreatic NETs (who experienced progression on or after chemotherapy) to everolimus or everolimus in combination with long-acting octreotide, showed a significantly longer median PFS in patients receiving combination therapy as compared to everolimus alone (16.7 months versus 9.7 months) [104]. More recently, a multicenter double-blind placebo-controlled phase III trial (RADIANT-3) comparing everolimus to placebo in 410 patients with progressive, advanced low or intermediate grade NETs showed that median PFS was improved with everolimus therapy (11.0 months versus 4.6 months) [72]. The most common adverse events in the everolimus group versus placebo group were stomatitis (64% versus 17%), rash (49% versus 10%), diarrhea (34% versus 10%), fatigue (31% versus 14%), and infections (23% versus 6%). The results of these studies have led to the approval of everolimus by the European Medicines Agency in the European Union and by the Food and Drug Administration in the USA for the treatment of progressive, unresectable, locally advanced or metastatic, low or intermediate grade pancreatic NETs.

In the follow-up, randomized, double-blind, placebo-controlled, phase III RADIANT-4 trial, 302 patients with advanced, progressive, well-differentiated, nonfunctional NETs were randomized to everolimus 10 mg per day orally or placebo, both with supportive care [74]. The primary endpoint was PSF, and OS and quality of life were secondary endpoints. Median PFS of 11.0 months was significantly improved in the everolimus group compared to 3.9 months in the placebo group (). Although not statistically significant, the results of the first preplanned interim OS analysis indicated that everolimus might be associated with a reduction in the risk of death [74].

6.2. Sunitinib: Targeting Key Drivers of Angiogenesis

The highly vascular nature of NETs led to initial interest in investigating neoangiogenesis in NETs. A number of studies have found elevated expression of several cellular growth factors and their receptors in NETs: VEGF, VEGF receptor (VEGFR), platelet-derived growth factor (PDGF), PDGF receptor (PDGFR), stem cell factor receptor (c-KIT), and epidermal growth factor receptor (EGFR) [96]. Many of these receptors with their respective growth factor ligands function as tyrosine kinases (RTKs) directly and indirectly regulating tumor growth, survival, and angiogenesis. The hypothesis that inhibiting these targets in concert will result in broad antitumor efficacy in patients with NETs has been studied in several clinical trials (Table 2).

Sunitinib malate is a small molecule kinase inhibitor with activity against a number of tyrosine kinase receptors, including VEGFR, PDGFR, KIT, RET, and FMS-like tyrosine kinase-3 (FLT3) [105]. A phase II trial in patients with advanced NETs who received sunitinib demonstrated a median time to tumor progression of 7.7 and 10.2 months in patients with pancreatic NETs and carcinoid tumors, respectively [96]. A follow-up randomized, double-blind phase III trial comparing the response of 86 randomly selected patients given sunitinib with that of 85 patients on placebo demonstrated significant improvement in median PFS of patients on sunitinib (11.4 months versus 5.5 months) [71]. Moreover, patients treated with sunitinib showed early signs of an increase in overall survival. The most common adverse events associated with sunitinib treatment were diarrhea, nausea, asthenia, vomiting, and fatigue; each occurred in 30% or more of patients [71]. Based on these findings, sunitinib was approved by the European Medicines Agency and by the Food and Drug Administration for the treatment of progressive, unresectable, locally advanced or metastatic pancreatic NETs.

None of the clinical trials with everolimus and sunitinib for treatment of patients with advanced NETs assessed whether response to therapy was related to the altered intracellular signaling pathways or tumor genotype. An open-label, prospective, phase II clinical trial for treatment of low or intermediate grade advanced, progressive NETs with everolimus or sunitinib based on the genetic alterations present in the tumor (NCT02315625) is now underway [51].

6.3. Other Molecular Therapeutics Investigated for Treatment of Advanced NETs

In addition to the approval of sunitinib and everolimus, a number of other agents targeting different RTKs, growth factors, and mTOR signaling pathway have been investigated as an alternative therapy for patients with advanced NETs.

In a phase II clinical trial of temsirolimus, an mTOR inhibitor, in 36 patients with advanced NETs, a modest intent-to-treat response rate of 5.6%, tumor control (stable disease (SD) plus PR) rate of 63.9%, median time to progression of 6 months, and 1-year OS rate of 71.5%, was observed. The most frequent drug-related adverse events of all grades included fatigue (78%), hyperglycemia (69%), and rash (64%) [106].

The activity of sorafenib, an orally active multityrosine kinase inhibitor targeting VEGFR-2, VEGFR-3, PDGFR-β, FLT3, c-KIT, RET B-RAF, and C-RAF, has been investigated in another phase II clinical trial in patients with gastrointestinal () and pancreatic () NETs [107]. It has been demonstrated that combined minor response and PR rates of gastrointestinal and pancreatic NETs were 17% and 32%, respectively, with a PFS of 6 months in 60.8% of patients with pancreatic NETs [107]. Most common grade 3-4 adverse events experienced by 43% of patients included skin reactions (20%), fatigue (9%), and gastrointestinal tract symptoms (7%) [107].

Another multikinase inhibitor, pazopanib, targeting VEGFR-1, VEGFR-2, VEGFR-3, PDGFR, and c-KIT, was studied in a phase II clinical trial in 37 patients with metastatic NETs and an overall response rate (ORR) of 24.3% and a disease control rate (complete response (CR) + PR + SD) of 75.7% was observed [108]. The most common grades 3 and 4 adverse events were proteinuria (11%), neutropenia (8%), hypertension (5%), diarrhea (5%), anorexia (5%), abdominal pain (5%), and elevation in liver transaminases (5%) [108]. An EGFR inhibitor, gefitinib, has been investigated in a phase II clinical trial in patients with advanced NETs and showed PFS of 6 months in 23 of 38 (61%) patients with gastrointestinal NETs and 9 of 29 (31%) patients with pancreatic NETs [109]. Grade 3 or 4 toxicities were infrequent and included fatigue (6%), diarrhea (5%), and rash (3%).

While the above clinical trials showed moderate clinical activity of monotherapies with sorafenib, pazopanib, gefitinib, and temsirolimus, combination therapy with somatostatin analogs and/or selective monoclonal antibodies targeting different growth factors have shown more promising results.

A recent multicenter phase II clinical trial of combination therapy with temsirolimus and bevacizumab in patients with progressive well- or moderately differentiated NETs () showed very promising results with median PFS of 13.2 months and median OS of 34 months [110]. The most common grade 3 to 4 adverse events attributed to therapy were hypertension (21%), fatigue (16%), lymphopenia (14%), and hyperglycemia (14%) [110].

A prospective, multi-institutional phase II study of pazopanib and depot octreotide in patients with advanced low grade NETs () demonstrated a median PFS of 12.7 and 11.7 months for gastrointestinal NETs and pancreatic NETs, respectively [111]. Significant, grade 3 or 4 toxicities were rare and included hypertension (), neutropenia (), fatigue (), diarrhea (), transaminitis (), hypertriglyceridemia (), anemia (), nausea (), pain (), rash (), syncope (), and confusion ().

Combination of depot octreotide, bevacizumab, and pertuzumab, a monoclonal antibody inhibiting the dimerization of HER2 with other HER receptors, was evaluated in a phase II clinical trial in patients with advanced well-differentiated NETs and demonstrated an ORR of 16% and a median PFS of 8.2 months [112].

7. Systemic Chemotherapy

Despite the demonstration of improved PFS in patients with advanced NETs treated with routinely used first-line therapeutic agents including octreotide, lanreotide, and everolimus or sunitinib, the overall tumor response rates with these agents have been less than satisfactory (Table 2) and for patients with bulky, rapidly progressive disease, and poorly differentiated NETs, these treatments are not likely to yield meaningful responses [64].

Multiple reports and phase I and II clinical trials of a variety of cytotoxic chemotherapy regimens have yielded promising results for the treatment of patients with high burden, rapidly progressing NETs. The effects of chemotherapies with alkylating agents, such as streptozocin, dacarbazine, and temozolomide, alone or in combination with the antimetabolites 5-FU, capecitabine, or the anthracycline drugs doxorubicin and epirubicin, have been evaluated, and encouraging results of ORR rates of up to 70% and PFS of more than 26 months have been reported for some but not all regimens [113–116]. A recent phase II clinical trial investigating the effect of chemotherapy with 5-FU and streptozocin combined with anti-VEGF monoclonal antibody bevacizumab in patients with advanced, progressive, well-differentiated NETs () showed very encouraging results with a median PFS of 23.7 months [117].

Solid evidence from phase III randomized controlled trial is currently lacking and there is no consensus on which patient population should be treated and what treatment regimen should be chosen, and the optimal timing of the treatment remains to be established [115].

8. Discussion and Conclusion

Our understanding of the biology and natural history of NETs has improved considerably in the last several decades and the spectrum of available therapeutic options is rapidly expanding. The management of patients with metastatic NETs has been revolutionized by the development of new systemic and biological treatment strategies such as molecular targeted therapies with everolimus and sunitinib, PRRT, as well as revealing the antiproliferative properties of SA. The growing list of effective therapeutics with favorable toxicity profiles has given rise to novel multidisciplinary approaches in the management of patients with advanced NETs including the emerging concept of sequential treatment [118]. Growing body of evidence from randomized clinical trials comparing the effects of different therapeutic modalities makes it unclear when to apply a given option, what combination therapeutic approach should be used and in what sequence, how long treatment should be continued, and in what subgroup of patients a particular treatment option should be used.

While it is clear that a clinical trial of every possible combination therapy sequence would be practically impossible to design and conduct, several consensus statements by experts from the USA, Canada, and Europe have been recently developed for the management of patients with advanced low or intermediate grade NETs [27, 55, 64, 119–123].

Given the heterogeneity and intricate biology of NETs, as well as the complexity of management of every individual case, a general approach of treatment individualization by a dedicated multidisciplinary team is currently gaining increasing acceptance among physicians. This includes a thorough review of all patient-related and disease-related factors for every individual case such as consideration of disease extent, location, and progression, as well as tumor grade, patent’s symptoms, comorbidities, and performance status. Careful consideration and, when it is needed, reevaluation of the potential benefits of specific therapeutic and supportive options at each clinical decision point along the disease course are essential to ensure most favorable outcomes [27, 120, 124].

More high level evidence will be needed to further define and clarify the utility, appropriateness, and the sequence of the growing list of available therapies for this patient population; however, data from well-designed randomized phase III clinical trials is rapidly accumulating that will stimulate further investigations into potential development of new management strategies. It is therefore important to thoroughly review emerging evidence from recent clinical trials and report major findings in frequent updates, which will expand our knowledge and contribute to a better understanding, characterization, and management of advanced NETs and, ultimately, help patients and their families.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

References

T. R. Halfdanarson, K. G. Rabe, J. Rubin, and G. M. Petersen, “Pancreatic neuroendocrine tumors (PNETs): incidence, prognosis and recent trend toward improved survival,” Annals of Oncology, vol. 19, no. 10, pp. 1727–1733, 2008.
View at: Publisher Site | Google Scholar
K. Öberg, “Genetics and molecular pathology of neuroendocrine gastrointestinal and pancreatic tumors (gastroenteropancreatic neuroendocrine tumors),” Current Opinion in Endocrinology, Diabetes and Obesity, vol. 16, no. 1, pp. 72–78, 2009.
View at: Publisher Site | Google Scholar
M. H. Kulke, L. B. Anthony, D. L. Bushnell et al., “NANETS treatment guidelines: Well-differentiated neuroendocrine tumors of the stomach and pancreas,” Pancreas, vol. 39, no. 6, pp. 735–752, 2010.
View at: Publisher Site | Google Scholar
D. C. Metz and R. T. Jensen, “Gastrointestinal neuroendocrine tumors: pancreatic endocrine tumors,” Gastroenterology, vol. 135, no. 5, pp. 1469–1492, 2008.
View at: Publisher Site | Google Scholar
I. M. Modlin, S. F. Moss, D. C. Chung, R. T. Jensen, and E. Snyderwine, “Priorities for improving the management of gastroenteropancreatic neuroendocrine tumors,” Journal of the National Cancer Institute, vol. 100, no. 18, pp. 1282–1289, 2008.
View at: Publisher Site | Google Scholar
W. W. de Herder, “Tumours of the midgut (jejunum, ileum and ascending colon, including carcinoid syndrome),” Best Practice and Research: Clinical Gastroenterology, vol. 19, no. 5, pp. 705–715, 2005.
View at: Publisher Site | Google Scholar
J. C. Yao, M. Hassan, A. Phan et al., “One hundred years after ‘carcinoid’: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States,” Journal of Clinical Oncology, vol. 26, no. 18, pp. 3063–3072, 2008.
View at: Publisher Site | Google Scholar
V. L. Tsikitis, B. C. Wertheim, and M. A. Guerrero, “Trends of incidence and survival of gastrointestinal neuroendocrine tu-mors in the united states: a seer analysis,” Journal of Cancer, vol. 3, no. 1, pp. 292–302, 2012.
View at: Publisher Site | Google Scholar
K. Öberg and D. Castellano, “Current knowledge on diagnosis and staging of neuroendocrine tumors,” Cancer and Metastasis Reviews, vol. 30, 1, no. 1, pp. 3–7, 2011.
View at: Publisher Site | Google Scholar
J. Hallet, C. H. L. Law, M. Cukier, R. Saskin, N. Liu, and S. Singh, “Exploring the rising incidence of neuroendocrine tumors: a population-based analysis of epidemiology, metastatic presentation, and outcomes,” Cancer, vol. 121, no. 4, pp. 589–597, 2015.
View at: Publisher Site | Google Scholar
T. Ito, L. Lee, M. Hijioka et al., “The up-to-date review of epidemiological pancreatic neuroendocrine tumors in Japan,” Journal of Hepato-Biliary-Pancreatic Sciences, vol. 22, no. 8, pp. 574–577, 2015.
View at: Publisher Site | Google Scholar
I. M. Modlin, S. F. Moss, B. I. Gustafsson, B. Lawrence, S. Schimmack, and M. Kidd, “The archaic distinction between functioning and nonfunctioning neuroendocrine neoplasms is no longer clinically relevant,” Langenbeck's Archives of Surgery, vol. 396, no. 8, pp. 1145–1156, 2011.
View at: Publisher Site | Google Scholar
K. E. Öberg, “Gastrointestinal neuroendocrine tumors,” Annals of Oncology, vol. 21, 7, no. 7, pp. vii72–vii80, 2010.
View at: Publisher Site | Google Scholar
J. R. Strosberg, A. Cheema, J. Weber, G. Han, D. Coppola, and L. K. Kvols, “Prognostic validity of a Novel American Joint Committee on Cancer staging classification for pancreatic neuroendocrine tumors,” Journal of Clinical Oncology, vol. 29, no. 22, pp. 3044–3049, 2011.
View at: Publisher Site | Google Scholar
M. Falconi, D. K. Bartsch, B. Eriksson et al., “ENETS consensus guidelines for the management of patients with digestive neuroendocrine neoplasms of the digestive system: well-differentiated pancreatic non-functioning tumors,” Neuroendocrinology, vol. 95, no. 2, pp. 120–134, 2012.
View at: Publisher Site | Google Scholar
A. Saxena, T. C. Chua, F. Chu, A. Al-Zahrani, and D. L. Morris, “Optimizing the surgical effort in patients with advanced neuroendocrine neoplasm hepatic metastases: A critical analysis of 40 patients treated by hepatic resection and cryoablation,” American Journal of Clinical Oncology: Cancer Clinical Trials, vol. 35, no. 5, pp. 439–445, 2012.
View at: Publisher Site | Google Scholar
V. Sallinen, C. Haglund, and H. Seppänen, “Outcomes of resected nonfunctional pancreatic neuroendocrine tumors: do size and symptoms matter?” Surgery (United States), vol. 158, no. 6, pp. 1556–1563, 2015.
View at: Publisher Site | Google Scholar
J. X. Wu and F. C. Brunicardi, “Surgical approaches to pancreatic neuroendocrine tumors,” in Management of Pancreatic Neuroendocrine Tumors, pp. 117–126, Springer, New York, NY, USA, 2015.
View at: Publisher Site | Google Scholar
S. Partelli, M. Inama, A. Rinke et al., “Long-term outcomes of surgical management of pancreatic neuroendocrine tumors with synchronous liver metastases,” Neuroendocrinology, vol. 102, pp. 68–76, 2015.
View at: Publisher Site | Google Scholar
D. J. Birnbaum, O. Turrini, L. Vigano et al., “Surgical management of advanced pancreatic neuroendocrine tumors: short-term and long-term results from an international multi-institutional study,” Annals of Surgical Oncology, vol. 22, no. 3, pp. 1000–1007, 2015.
View at: Publisher Site | Google Scholar
C.-H. Yuan, J. Wang, D.-R. Xiu et al., “Meta-analysis of liver resection versus nonsurgical treatments for pancreatic neuroendocrine tumors with liver metastases,” Annals of Surgical Oncology, vol. 23, no. 1, pp. 244–249, 2016.
View at: Publisher Site | Google Scholar
M. Pavel, E. Baudin, A. Couvelard et al., “ENETS consensus guidelines for the management of patients with liver and other distant metastases from neuroendocrine neoplasms of foregut, midgut, hindgut, and unknown primary,” Neuroendocrinology, vol. 95, no. 2, pp. 157–176, 2012.
View at: Publisher Site | Google Scholar
K. S. Gurusamy, V. Pamecha, D. Sharma, and B. R. Davidson, Palliative cytoreductive surgery versus other palliative treatments in patients with unresectable liver metastases from gastro‐entero‐pancreatic neuroendocrine tumours, Article ID CD007118, 2009.
View at: Publisher Site
J. Franko, W. Feng, L. Yip, E. Genovese, and A. J. Moser, “Non-functional neuroendocrine carcinoma of the pancreas: incidence, tumor biology, and outcomes in 2,158 patients,” Journal of Gastrointestinal Surgery, vol. 14, no. 3, pp. 541–548, 2010.
View at: Publisher Site | Google Scholar
M. Lesurtel, D. M. Nagorney, V. Mazzaferro, R. T. Jensen, and G. J. Poston, “When should a liver resection be performed in patients with liver metastases from neuroendocrine tumours? A systematic review with practice recommendations,” HPB, vol. 17, no. 1, pp. 17–22, 2015.
View at: Publisher Site | Google Scholar
G. Capurso, M. Rinzivillo, R. Bettini, L. Boninsegna, G. D. Fave, and M. Falconi, “Systematic review of resection of primary midgut carcinoid tumour in patients with unresectable liver metastases,” British Journal of Surgery, vol. 99, no. 11, pp. 1480–1486, 2012.
View at: Publisher Site | Google Scholar
M. Pavel, D. O'Toole, F. Costa et al., “ENETS consensus guidelines update for the management of distant metastatic disease of intestinal, pancreatic, bronchial neuroendocrine neoplasms (NEN) and NEN of unknown primary site,” Neuroendocrinology, vol. 103, no. 2, pp. 172–185, 2016.
View at: Publisher Site | Google Scholar
A. Saxena, T. C. Chua, M. Perera, F. Chu, and D. L. Morris, “Surgical resection of hepatic metastases from neuroendocrine neoplasms: a systematic review,” Surgical Oncology, vol. 21, no. 3, 2012.
View at: Publisher Site | Google Scholar
G. Yang, M. Ji, J. Chen et al., “Surgery management for sporadic small (≤ cm, non-functioning pancreatic neuroendocrine tumors: a consensus statement by the chinese study group for neuroendocrine tumors (CSNET),” International Journal of Oncology, vol. 50, no. 2, pp. e131–e141, 2017.
View at: Google Scholar
C. A. Moran, S. Suster, D. Coppola, and M. R. Wick, “Neuroendocrine carcinomas of the lung a critical analysis,” American Journal of Clinical Pathology, vol. 131, no. 2, pp. 206–221, 2009.
View at: Publisher Site | Google Scholar
J. M. Sarmiento, F. G. Que, C. S. Grant et al., “Concurrent resections of pancreatic islet cell cancers with synchronous hepatic metastases: outcomes of an aggressive approach,” Surgery, vol. 132, no. 6, pp. 976–983, 2002.
View at: Publisher Site | Google Scholar
J. M. Sarmiento, G. Heywood, J. Rubin, D. M. Ilstrup, D. M. Nagorney, and F. G. Que, “Surgical treatment of neuroendocrine metastases to the liver: a plea for resection to increase survival,” Journal of the American College of Surgeons, vol. 197, no. 1, pp. 29–37, 2003.
View at: Publisher Site | Google Scholar
S. Q. Nguyen, L. P. Angel, C. M. Divino, S. Schluender, and R. R. P. Warner, “Surgery in malignant pancreatic neuroendocrine tumors,” Journal of Surgical Oncology, vol. 96, no. 5, pp. 397–403, 2007.
View at: Publisher Site | Google Scholar
S. A. Gulec, T. S. Mountcastle, D. Frey, and J. D. Cundiff, “Cytoreductive surgery in patients with advanced-stage carcinoid tumors/Discussion,” American Surgeon, vol. 68, no. 8, artilce 667, 2002.
View at: Google Scholar
S. C. Mayo, M. C. De Jong, C. Pulitano et al., “Surgical management of hepatic neuroendocrine tumor metastasis: Results from an international multi-institutional analysis,” Annals of Surgical Oncology, vol. 17, no. 12, pp. 3129–3136, 2010.
View at: Publisher Site | Google Scholar
G. Spolverato, F. Bagante, D. Wagner et al., “Quality of life after treatment of neuroendocrine liver metastasis,” Journal of Surgical Research, vol. 198, no. 1, pp. 155–164, 2015.
View at: Publisher Site | Google Scholar
E. Sporn, G. J. Mancini, Y. Khajanchee et al., “Multimodal cytoreduction for carcinoid liver metastases: analysis of a case series with highly advanced disease,” European Surgery, vol. 40, no. 2, pp. 72–76, 2008.
View at: Publisher Site | Google Scholar
S. Scigliano, R. Lebtahi, F. Maire et al., “Clinical and imaging follow-up after exhaustive liver resection of endocrine metastases: a 15-year monocentric experience,” Endocrine-Related Cancer, vol. 16, no. 3, pp. 977–990, 2009.
View at: Publisher Site | Google Scholar
E. S. Glazer, J. F. Tseng, W. Al-Refaie et al., “Long-term survival after surgical management of neuroendocrine hepatic metastases,” HPB, vol. 12, no. 6, pp. 427–433, 2010.
View at: Publisher Site | Google Scholar
D. Cusati, L. Zhang, W. S. Harmsen et al., “Metastatic nonfunctioning pancreatic neuroendocrine carcinoma to liver: surgical treatment and outcomes,” Journal of the American College of Surgeons, vol. 215, no. 1, pp. 117–125, 2012.
View at: Publisher Site | Google Scholar
F. M. Watzka, C. Fottner, M. Miederer et al., “Surgical therapy of neuroendocrine neoplasm with hepatic metastasis: patient selection and prognosis,” Langenbeck's Archives of Surgery, vol. 400, no. 3, pp. 349–358, 2015.
View at: Publisher Site | Google Scholar
D. Elias, A. David, I. Sourrouille et al., “Neuroendocrine carcinomas: optimal surgery of peritoneal metastases (and associated intra-abdominal metastases),” Surgery, vol. 155, no. 1, pp. 5–12, 2014.
View at: Publisher Site | Google Scholar
F. Bagante, G. Spolverato, K. Merath, L. M. Postlewait, G. A. Poultsides, M. G. Mullen et al., “Neuroendocrine liver metastasis: the chance to be cured after liver surgery,” Journal of Surgical Oncology, 2017.
View at: Publisher Site | Google Scholar
E. A. Woltering, B. A. Voros, D. T. Beyer et al., “Aggressive surgical approach to the management of neuroendocrine tumors: a report of 1,000 surgical cytoreductions by a single institution,” Journal of the American College of Surgeons, vol. 224, no. 4, pp. 434–447, 2017.
View at: Publisher Site | Google Scholar
H. Chung and W. C. Chapman, “Liver transplantation for metastatic neuroendocrine tumors,” Advances in Surgery, vol. 48, no. 1, pp. 235–252, 2014.
View at: Publisher Site | Google Scholar
Y. R. Nobel and D. S. Goldberg, “Variable use of model for end-stage liver disease exception points in patients with neuroendocrine tumors metastatic to the liver and its impact on patient outcomes,” Transplantation, vol. 99, no. 11, pp. 2341–2346, 2015.
View at: Publisher Site | Google Scholar
S. T. Fan, Y. P. Le Treut, V. Mazzaferro et al., “Liver transplantation for neuroendocrine tumour liver metastases,” HPB, vol. 17, no. 1, pp. 23–28, 2014.
View at: Publisher Site | Google Scholar
Y. P. Le Treut, E. Grégoire, J. Klempnauer et al., “Liver transplantation for neuroendocrine tumors in Europe-results and trends in patient selection: a 213-case European liver transplant registry study,” Annals of Surgery, vol. 257, no. 5, pp. 807–815, 2013.
View at: Publisher Site | Google Scholar
N. T. Nguyen, T. R. Harring, J. A. Goss, and C. A. O'Mahony, “Neuroendocrine Liver Metastases and Orthotopic Liver Transplantation: The US Experience,” International Journal of Hepatology, vol. 2011, Article ID 742890, 7 pages, 2011.
View at: Publisher Site | Google Scholar
R. Gedaly, M. F. Daily, D. Davenport et al., “Liver transplantation for the treatment of liver metastases from neuroendocrine tumors: an analysis of the UNOS database,” Archives of Surgery, vol. 146, no. 8, pp. 953–958, 2011.
View at: Publisher Site | Google Scholar
V. Neychev, S. M. Steinberg, C. Cottle-Delisle et al., “Mutation-targeted therapy with sunitinib or everolimus in patients with advanced low-grade or intermediategrade neuroendocrine tumours of the gastrointestinal tract and pancreas with or without cytoreductive surgery: protocol for a phase II clinical trial,” BMJ Open, vol. 5, no. 5, Article ID e008248, 2015.
View at: Publisher Site | Google Scholar
E. S. Engelman, R. Leon-Ferre, B. G. Naraev et al., “Comparison of transarterial liver-directed therapies for low-grade metastatic neuroendocrine tumors in a single institution,” Pancreas, vol. 43, no. 2, pp. 219–225, 2014.
View at: Publisher Site | Google Scholar
J. Nazario and S. Gupta, “Transarterial liver-directed therapies of neuroendocrine hepatic metastases,” Seminars in Oncology, vol. 37, no. 2, pp. 118–126, 2010.
View at: Publisher Site | Google Scholar
E. A. Eisenhauer, P. Therasse, J. Bogaerts et al., “New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1),” European Journal of Cancer, vol. 45, no. 2, pp. 228–247, 2009.
View at: Publisher Site | Google Scholar
A. Kennedy, L. Bester, R. Salem, R. A. Sharma, R. W. Parks, and P. Ruszniewski, “Role of hepatic intra-arterial therapies in metastatic neuroendocrine tumours (NET): guidelines from the NET-liver-metastases consensus conference,” HPB, vol. 17, no. 1, pp. 29–37, 2015.
View at: Publisher Site | Google Scholar
A. B. Benson, J.-F. Geschwind, M. F. Mulcahy et al., “Radioembolisation for liver metastases: results from a prospective 151 patient multi-institutional phase II study,” European Journal of Cancer, vol. 49, no. 15, pp. 3122–3130, 2013.
View at: Publisher Site | Google Scholar
Z. Devcic, J. Rosenberg, A. J. A. Braat et al., “The efficacy of hepatic 90Y resin radioembolization for metastatic neuroendocrine tumors: a meta-analysis,” Journal of Nuclear Medicine, vol. 55, no. 9, pp. 1404–1410, 2014.
View at: Publisher Site | Google Scholar
L. N. Møller, C. E. Stidsen, B. Hartmann, and J. J. Holst, “Somatostatin receptors,” Biochimica et Biophysica Acta-Biomembranes, vol. 1616, no. 1, pp. 1–84, 2003.
View at: Publisher Site | Google Scholar
K. E. Öberg, “The management of neuroendocrine tumours: current and future medical therapy options,” Clinical Oncology, vol. 24, no. 4, pp. 282–293, 2012.
View at: Publisher Site | Google Scholar
M. H. Kulke, “Systemic therapy for advanced pancreatic neuroendocrine tumors,” Seminars in Oncology, vol. 40, no. 1, pp. 75–83, 2013.
View at: Publisher Site | Google Scholar
I. I. Schnirer, J. C. Yao, and J. A. Ajani, “Carcinoid: a comprehensive review,” Acta Oncologica, vol. 42, no. 7, pp. 672–692, 2003.
View at: Publisher Site | Google Scholar
M. E. Caplin, M. Pavel, and P. Ruszniewski, “Lanreotide in metastatic enteropancreatic neuroendocrine tumors,” New England Journal of Medicine, vol. 371, no. 16, pp. 1556-1557, 2014.
View at: Publisher Site | Google Scholar
S. Narayanan and P. L. Kunz, “Role of somatostatin analogues in the treatment of neuroendocrine tumors,” Journal of the National Comprehensive Cancer Network, vol. 13, no. 1, pp. 109–117, 2015.
View at: Publisher Site | Google Scholar
S. Narayanan and P. L. Kunz, “Beyond biologics: is there a role for systemic cytotoxic chemotherapy in neuroendocrine tumors?” International Journal of Endocrine Oncology, vol. 2, no. 1, pp. 13–20, 2015.
View at: Publisher Site | Google Scholar
A. Rinke, H.-H. Müller, C. Schade-Brittinger et al., “Placebo-controlled, double-blind, prospective, randomized study on the effect of octreotide LAR in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors: a report from the PROMID study group,” Journal of Clinical Oncology, vol. 27, no. 28, pp. 4656–4663, 2009.
View at: Publisher Site | Google Scholar
A. Rinke, M. Wittenberg, C. Schade-Brittinger et al., “Placebo controlled, double blind, prospective, randomized study on the effect of octreotide lar in the control of tumor growth in patients with metastatic neuroendocrine midgut tumors (PROMID): results on long term survival,” Neuroendocrinology, vol. 104, no. 1, pp. 26–32, 2017.
View at: Publisher Site | Google Scholar
G. Kaltsas and A. B. Grossman, “The expanding role of somatostatin analogues in the treatment of neuroendocrine tumours: the CLARINET study,” Clinical Endocrinology, vol. 83, no. 6, pp. 759–761, 2015.
View at: Publisher Site | Google Scholar
H. Igarashi, M. Hijioka, L. Lee, and T. Ito, “Biotherapy of pancreatic neuroendocrine tumors using somatostatin analogs,” Journal of Hepato-Biliary-Pancreatic Sciences, vol. 22, no. 8, pp. 618–622, 2015.
View at: Publisher Site | Google Scholar
L. K. Kvols, K. E. Oberg, T. M. O'Dorisio et al., “Pasireotide (SOM230) shows efficacy and tolerability in the treatment of patients with advanced neuroendocrine tumors refractory or resistant to octreotide LAR: results from a phase II study,” Endocrine-Related Cancer, vol. 19, no. 5, pp. 657–666, 2012.
View at: Publisher Site | Google Scholar
M. Cives, P. L. Kunz, B. Morse et al., “Phase II clinical trial of pasireotide long-acting repeatable in patients with metastatic neuroendocrine tumors,” Endocrine-Related Cancer, vol. 22, no. 1, pp. 1–9, 2015.
View at: Publisher Site | Google Scholar
E. Raymond, L. Dahan, and J.-L. Raoul, “Sunitinib malate for the treatment of pancreatic neuroendocrine tumors,” The New England Journal of Medicine, vol. 334, pp. 501–513, 2011.
View at: Publisher Site | Google Scholar
J. C. Yao, M. H. Shah, and T. Ito, “Everolimus for advanced pancreatic neuroendocrine tumors,” The New England Journal of Medicine, vol. 364, no. 6, pp. 514–523, 2011.
View at: Publisher Site | Google Scholar
M. E. Pavel, J. D. Hainsworth, E. Baudin et al., “Everolimus plus octreotide long-acting repeatable for the treatment of advanced neuroendocrine tumours associated with carcinoid syndrome (RADIANT-2): a randomised, placebo-controlled, phase 3 study,” The Lancet, vol. 378, no. 9808, pp. 2005–2012, 2011.
View at: Publisher Site | Google Scholar
J. C. Yao, N. Fazio, S. Singh et al., “Everolimus for the treatment of advanced, non-functional neuroendocrine tumours of the lung or gastrointestinal tract (RADIANT-4): a randomised, placebo-controlled, phase 3 study,” The Lancet, vol. 387, no. 10022, pp. 968–977, 2016.
View at: Publisher Site | Google Scholar
P. Lapuerta, B. Zambrowicz, D. Fleming, D. Wheeler, and A. Sands, “Telotristat etiprate, a novel inhibitor of serotonin synthesis for the treatment of carcinoid syndrome,” Clinical Investigation, vol. 5, no. 5, pp. 447–456, 2015.
View at: Publisher Site | Google Scholar
M. H. Kulke, T. O'Dorisio, A. Phan et al., “Telotristat etiprate, a novel serotonin synthesis inhibitor, in patients with carcinoid syndrome and diarrhea not adequately controlled by octreotide,” Endocrine-Related Cancer, vol. 21, no. 5, pp. 705–714, 2014.
View at: Publisher Site | Google Scholar
M. Pavel, D. Hörsch, M. Caplin, J. Ramage, T. Seufferlein, J. Valle et al., “Telotristat etiprate for carcinoid syndrome: a single-arm, multicenter trial,” Journal of Clinical Endocrinology and Metabolism, vol. 100, no. 4, pp. 1511–1519, 2015.
View at: Publisher Site | Google Scholar
M. Kulke, D. Hörsch, M. Caplin et al., “Integrated placebo-controlled safety analysis from clinical studies of telotristat ethyl for the treatment of carcinoid syndrome,” Annals of Oncology, vol. 27, supplement 6, article 422PD, 2016.
View at: Publisher Site | Google Scholar
W. A. Van Der Zwan, L. Bodei, J. Mueller-Brand, W. W. De Herder, L. K. Kvols, and D. J. Kwekkeboom, “Radionuclide therapy in neuroendocrine tumors,” European Journal of Endocrinology, vol. 172, no. 1, pp. R1–R8, 2015.
View at: Publisher Site | Google Scholar
D. J. Kwekkeboom, W. W. de Herder, B. L. Kam et al., “Treatment with the radiolabeled somatostatin analog [177Lu- DOTA0,Tyr3]octreotate: toxicity, efficacy, and survival,” Journal of Clinical Oncology, vol. 26, no. 13, pp. 2124–2130, 2008.
View at: Publisher Site | Google Scholar
H. Ilhan, W. P. Fendler, C. C. Cyran et al., “Impact of 68Ga-DOTATATE PET/CT on the surgical management of primary neuroendocrine tumors of the pancreas or ileum,” Annals of Surgical Oncology, vol. 22, no. 1, pp. 164–171, 2015.
View at: Publisher Site | Google Scholar
E. Ilan, M. Sandström, C. Wassberg et al., “Dose response of pancreatic neuroendocrine tumors treated with peptide receptor radionuclide therapy using 177Lu-DOTATATE,” Journal of Nuclear Medicine, vol. 56, no. 2, pp. 177–182, 2015.
View at: Publisher Site | Google Scholar
J. Strosberg, G. El-Haddad, E. Wolin et al., “Phase 3 trial of 177Lu-dotatate for midgut neuroendocrine tumors,” New England Journal of Medicine, vol. 376, no. 2, pp. 125–135, 2017.
View at: Publisher Site | Google Scholar
C. Swärd, P. Bernhardt, H. Ahlman et al., “[177Lu-DOTA0-Tyr3]-Octreotate treatment in patients with disseminated gastroenteropancreatic neuroendocrine tumors: the value of measuring absorbed dose to the kidney,” World Journal of Surgery, vol. 34, no. 6, pp. 1368–1372, 2010.
View at: Publisher Site | Google Scholar
M. Garkavij, M. Nickel, K. Sjögreen-Gleisner et al., “177Lu-[DOTA0,Tyr3] octreotate therapy in patients with disseminated neuroendocrine tumors: analysis of dosimetry with impact on future therapeutic strategy,” Cancer, vol. 116, no. 4, pp. 1084–1092, 2010.
View at: Publisher Site | Google Scholar
L. Bodei, M. Cremonesi, C. M. Grana et al., “Peptide receptor radionuclide therapy with177Lu-DOTATATE: the IEO phase I-II study,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 38, no. 12, pp. 2125–2135, 2011.
View at: Publisher Site | Google Scholar
J. B. Cwikla, A. Sankowski, N. Seklecka et al., “Efficacy of radionuclide treatment DOTATATE Y-90 in patients with progressive metastatic gastroenteropancreatic neuroendocrine carcinomas (GEP-NETs): a phase II study,” Annals of Oncology, vol. 21, no. 4, pp. 787–794, 2009.
View at: Publisher Site | Google Scholar
A. K. Pfeifer, T. Gregersen, H. Grønbæk et al., “Peptide receptor radionuclide therapy with90Y-DOTATOC and177Lu-DOTATOC in advanced neuroendocrine tumors: results from a Danish cohort treated in Switzerland,” Neuroendocrinology, vol. 93, no. 3, pp. 189–196, 2011.
View at: Publisher Site | Google Scholar
D. L. Bushnell Jr., T. M. O'Dorisio, M. S. O'Dorisio et al., “90Y-edotreotide for metastatic carcinoid refractory to octreotide,” Journal of Clinical Oncology, vol. 28, no. 10, pp. 1652–1659, 2010.
View at: Publisher Site | Google Scholar
R. Valkema, S. Pauwels, L. K. Kvols et al., “Survival and response after peptide receptor radionuclide therapy with [90Y-DOTA0,Tyr3]octreotide in patients with advanced gastroenteropancreatic neuroendocrine tumors,” Seminars in Nuclear Medicine, vol. 36, no. 2, pp. 147–156, 2006.
View at: Publisher Site | Google Scholar
L. Bodei, M. Cremonesi, S. Zoboli et al., “Receptor-mediated radionuclide therapy with 90Y-DOTATOC in association with amino acid infusion: a phase I study,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 30, no. 2, pp. 207–216, 2003.
View at: Publisher Site | Google Scholar
C. Waldherr, M. Pless, H. R. Maecke, A. Haldemann, and J. Mueller-Brand, “The clinical value of [90Y-DOTA]-D-Phe1-Tyr3-octreotide (90Y-DOTATOC) in the treatment of neuroendocrine tumours: a clinical phase II study,” Annals of Oncology, vol. 12, no. 7, pp. 941–945, 2001.
View at: Publisher Site | Google Scholar
J. R. Strosberg, E. M. Wolin, B. Chasen et al., “NETTER-1 phase III: progression-free survival, radiographic response, and preliminary overall survival results in patients with midgut neuroendocrine tumors treated with 177-Lu-dotatate,” in Proceedings of the ASCO Annual Meeting, February 2016.
View at: Publisher Site | Google Scholar
J. Strosberg, E. Wolin, B. Chasen et al., “NETTER-1 phase III in patients with midgut neuroendocrine tumors treated with 177Lu-dotatate: efficacy, safety, QoL results and subgroup analysis,” Annals of Oncology, vol. 27, supplement 6, article 420PD, 2016.
View at: Publisher Site | Google Scholar
E.-M. Duerr, Y. Mizukami, A. Ng et al., “Defining molecular classifications and targets in gastroenteropancreatic neuroendocrine tumors through DNA microarray analysis,” Endocrine-Related Cancer, vol. 15, no. 1, pp. 243–256, 2008.
View at: Publisher Site | Google Scholar
M. H. Kulke, H.-J. Lenz, N. J. Meropol et al., “Activity of sunitinib in patients with advanced neuroendocrine tumors,” Journal of Clinical Oncology, vol. 26, no. 20, pp. 3403–3410, 2008.
View at: Publisher Site | Google Scholar
Y. Jiao, C. Shi, B. H. Edil et al., “DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors,” Science, vol. 331, no. 6021, pp. 1199–1203, 2011.
View at: Publisher Site | Google Scholar
K. Zitzmann, E. N. De Toni, S. Brand et al., “The novel mTOR inhibitor RAD001 (everolimus) induces antiproliferative effects in human pancreatic neuroendocrine tumor cells,” Neuroendocrinology, vol. 85, no. 1, pp. 54–60, 2007.
View at: Publisher Site | Google Scholar
F. Meric-Bernstam, A. Akcakanat, H. Chen et al., “PIK3CA/PTEN mutations and Akt activation as markers of sensitivity to allosteric mTOR inhibitors,” Clinical Cancer Research, vol. 18, no. 6, pp. 1777–1789, 2012.
View at: Publisher Site | Google Scholar
J. Capdevila, R. Salazar, I. Halperín, A. Abad, and J. C. Yao, “Innovations therapy: mammalian target of rapamycin (mTOR) inhibitors for the treatment of neuroendocrine tumors,” Cancer and Metastasis Reviews, vol. 30, supplement 1, pp. S27–S34, 2011.
View at: Publisher Site | Google Scholar
B. Lawrence, B. I. Gustafsson, A. Chan, B. Svejda, M. Kidd, and I. M. Modlin, “The epidemiology of gastroenteropancreatic neuroendocrine tumors,” Endocrinology and Metabolism Clinics of North America, vol. 40, no. 1, pp. 1–18, 2011.
View at: Publisher Site | Google Scholar
C. M. Johannessen, E. E. Reczek, M. F. James, H. Brems, E. Legius, and K. Cichowski, “The NF1 tumor suppressor critically regulates TSC2 and mTOR,” Proceedings of the National Academy of Sciences of the United States of America, vol. 102, no. 24, pp. 8573–8578, 2005.
View at: Publisher Site | Google Scholar
J. C. Yao, A. T. Phan, D. Z. Chang et al., “Efficacy of RAD001 (everolimus) and octreotide LAR in advanced low- to intermediate-grade neuroendocrine tumors: results of a phase II study,” Journal of Clinical Oncology, vol. 26, no. 26, pp. 4311–4318, 2008.
View at: Publisher Site | Google Scholar
J. C. Yao, C. Lombard-Bohas, E. Baudin et al., “Daily oral everolimus activity in patients with metastatic pancreatic neuroendocrine tumors after failure of cytotoxic chemotherapy: a phase II trial,” Journal of Clinical Oncology, vol. 28, no. 1, pp. 69–76, 2010.
View at: Publisher Site | Google Scholar
A.-M. O'Farrell, T. J. Abrams, H. A. Yuen et al., “SU11248 is a novel FLT3 tyrosine kinase inhibitor with potent activity in vitro and in vivo,” Blood, vol. 101, no. 9, pp. 3597–3605, 2003.
View at: Publisher Site | Google Scholar
I. Duran, J. Kortmansky, D. Singh et al., “A phase II clinical and pharmacodynamic study of temsirolimus in advanced neuroendocrine carcinomas,” British Journal of Cancer, vol. 95, no. 9, pp. 1148–1154, 2006.
View at: Publisher Site | Google Scholar
T. Hobday, J. Rubin, K. Holen et al., “MC044h, a phase II trial of sorafenib in patients (pts) with metastatic neuroendocrine tumors (NET): a Phase II Consortium (P2C) study,” in Proceedings of the ASCO Annual Meeting, 2007.
View at: Publisher Site | Google Scholar
H. K. Ahn, J. Y. Choi, K.-M. Kim et al., “Phase II study of pazopanib monotherapy in metastatic gastroenteropancreatic neuroendocrine tumours,” British Journal of Cancer, vol. 109, no. 6, pp. 1414–1419, 2013.
View at: Publisher Site | Google Scholar
T. J. Hobday, M. Mahoney, C. Erlichman et al., “A phase II trial of gefitinib in patients (pts) with progressive metastatic neuroendocrine tumors (NET): a phase II consortium (P2C) study,” in Proceedings of the ASCO Annual Meeting, 2006.
View at: Publisher Site | Google Scholar
T. J. Hobday, R. Qin, D. Reidy-Lagunes et al., “Multicenter phase II trial of temsirolimus and bevacizumab in pancreatic neuroendocrine tumors,” Journal of Clinical Oncology, vol. 33, no. 14, pp. 1551–1556, 2015.
View at: Publisher Site | Google Scholar
A. Phan, J. Yao, D. Fogelman et al., “A prospective, multi-institutional phase II study of GW786034 (pazopanib) and depot octreotide (sandostatin LAR) in advanced low-grade neuroendocrine carcinoma (LGNEC '10).,” in Proceedings of the ASCO Annual Meeting, 2010.
View at: Publisher Site | Google Scholar
I. Firdaus, K. C. Shih, A. Zakari, and et al, “Bevacizumab, pertuzumab, and sandostatin for patients (pts) with advanced neuroendocrine cancers (NET),” Journal of Clinical Oncology, vol. 30, article 4127, 2012.
View at: Publisher Site | Google Scholar
A. Koumarianou, G. Kaltsas, M. H. Kulke et al., “Temozolomide in advanced neuroendocrine neoplasms: pharmacological and clinical aspects,” Neuroendocrinology, vol. 101, no. 4, pp. 274–288, 2015.
View at: Publisher Site | Google Scholar
T. Meyer, W. Qian, M. E. Caplin et al., “Capecitabine and streptozocin ± cisplatin in advanced gastroenteropancreatic neuroendocrine tumours,” European Journal of Cancer, vol. 50, no. 5, pp. 902–911, 2014.
View at: Publisher Site | Google Scholar
T. Okusaka, H. Ueno, C. Morizane et al., “Cytotoxic chemotherapy for pancreatic neuroendocrine tumors,” Journal of Hepato-Biliary-Pancreatic Sciences, vol. 22, no. 8, pp. 628–633, 2015.
View at: Publisher Site | Google Scholar
R. L. Fine, A. P. Gulati, D. Tsushima, and et al, “Prospective phase II study of capecitabine and temozolomide (CAPTEM) for progressive, moderately, and well-differentiated metastatic neuroendocrine tumors,” in Proceedings of the ASCO Annual Meeting, 2014.
View at: Google Scholar
J. Seitz, D. Smith, D. O'Toole et al., “A Phase II trial of bevacizumab combined with chemotherapy in patients with metastatic well-differentiated duodeno-pancreatic endocrine tumors (BETTER study),” Annals of Oncology, supplement 9, abstract 1159P, p. ix378, 2012.
View at: Google Scholar
T. Alonso-Gordoa, J. J. Díez, J. Molina, P. Reguera, O. Martínez-Sáez, and E. Grande, “An Overview on the sequential treatment of pancreatic neuroendocrine tumors (pNETs),” Rare Cancers and Therapy, vol. 3, no. 1-2, pp. 13–33, 2015.
View at: Publisher Site | Google Scholar
J. R. Strosberg, G. A. Fisher, A. B. Benson et al., “Appropriateness of systemic treatments in unresectable metastatic well-differentiated pancreatic neuroendocrine tumors,” World Journal of Gastroenterology, vol. 21, no. 8, pp. 2450–2459, 2015.
View at: Publisher Site | Google Scholar
S. Singh, C. Dey, H. Kennecke et al., “Consensus recommendations for the diagnosis and management of pancreatic neuroendocrine tumors: guidelines from a canadian national expert group,” Annals of Surgical Oncology, vol. 22, no. 8, pp. 2685–2699, 2014.
View at: Publisher Site | Google Scholar
R. Garcia-Carbonero, P. JImenez-Fonseca, A. Teulé, J. Barriuso, and I. Sevilla, “SEOM clinical guidelines for the diagnosis and treatment of gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) 2014,” Clinical and Translational Oncology, vol. 16, no. 12, pp. 1025–1034, 2014.
View at: Publisher Site | Google Scholar
P. L. Kunz, D. Reidy-Lagunes, L. B. Anthony et al., “Consensus guidelines for the management and treatment of neuroendocrine tumors,” Pancreas, vol. 42, no. 4, pp. 557–577, 2013.
View at: Publisher Site | Google Scholar
L. K. Kvols and K. L. Brendtro, “The North American neuroendocrine tumor society (NANETS) guidelines: mission, goals, and process,” Pancreas, vol. 39, no. 6, pp. 705-706, 2010.
View at: Publisher Site | Google Scholar
S. Singh, S. L. Asa, C. Dey et al., “Diagnosis and management of gastrointestinal neuroendocrine tumors: an evidence-based Canadian consensus,” Cancer Treatment Reviews, vol. 47, pp. 32–45, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2017 Vladimir Neychev and Electron Kebebew. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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