Medication Exposures and Subsequent Development of Ewing Sarcoma: A Review of FDA Adverse Event Reports

Cope, Judith U.; Reaman, Gregory H.; Tonning, Joseph M.

doi:https://doi.org/10.1155/2015/948159

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Review Article | Open Access

Volume 2015 | Article ID 948159 | https://doi.org/10.1155/2015/948159

Medication Exposures and Subsequent Development of Ewing Sarcoma: A Review of FDA Adverse Event Reports

Judith U. Cope,¹Gregory H. Reaman,²and Joseph M. Tonning³

Academic Editor: Cyril Fisher

Received10 Jan 2015

Revised06 Mar 2015

Accepted26 Apr 2015

Published07 May 2015

Abstract

Background. Ewing sarcoma family of tumors (ESFT) are rare but deadly cancers of unknown etiology. Few risk factors have been identified. This study was undertaken to ascertain any possible association between exposure to therapeutic drugs and ESFT. Methods. This is a retrospective, descriptive study. A query of the FDA Adverse Event Reporting System (FAERS) was conducted for all reports of ESFT, January 1, 1998, through December 31, 2013. Report narratives were individually reviewed for patient characteristics, underlying conditions and drug exposures. Results. Over 16 years, 134 ESFT reports were identified, including 25 cases of ESFT following therapeutic drugs and biologics including immunosuppressive agents and hormones. Many cases were confounded by concomitant medications and other therapies. Conclusions. This study provides a closer look at medication use and underlying disorders in patients who later developed ESFT. While this study was not designed to demonstrate any clear causative association between ESFT and prior use of a single product or drug class, many drugs were used to treat immune-related disease and growth or hormonal disturbances. Further studies may be warranted to better understand possible immune or neuroendocrine abnormalities or exposure to specific classes of drugs that may predispose to the later development of ESFT.

1. Introduction and Study Objective

Ewing sarcoma family of tumors (ESFT) is a group of small, round blue cell tumors that arise in the bone or soft tissue. ESFT include classic Ewing sarcoma (ES) of bone, extraskeletal ES, skin tumors of the chest wall, and primitive neuroectodermal tumors (PNET) of the bone or soft tissue. About 90% of ESFT cases are characterized by the chromosome translocation t(11;22)(q24;q12) which involves the EWS/FLI-1 fusion gene and may share a common neural histogenesis [1–4]. While ESFT is rare, it is the second most common primary malignant bone tumor occurring in children and young adults and accounts for 10–15% of all primary bone tumors and 3% of all pediatric malignancies. ESFT occurs with a male predominance and highest incidence rates among whites with considerably lower rates in Blacks and East Asian populations. Age of onset is normally in the second decade of life, with 80% occurring in the first 2 decades of life and 80% occur in the skeleton [2–5]. Each year up to 400 patients in the US will be diagnosed with ESFT. The incidence has been steady over the past few decades [6].

While few risk factors for ESFT have been identified, the racial difference and specific chromosomal translocation might suggest a genetic predisposition [1, 7]. However, unlike other bone cancers (e.g., osteosarcoma) and soft tissue sarcomas (e.g., rhabdomyosarcoma) ESFT has not been found to be associated with any genetic disease or hereditary cancer syndrome [2, 7, 8]. Epidemiological studies have examined a wide array of possible risk factors, including childhood conditions and various parental exposures [9–16]. There is limited data about drug exposures as possible risk factors for ESFT. One study reported a possible association with poison or overdose of medications [11]. Another study by Valery et al. 2003 [16] found medication use to be more prevalent in controls than cases. While few if any studies have found an association with medications and ESFT (with exposure to medications), two studies [10, 16] found an inverse association with asthma, but this has not been confirmed by the other studies [9, 11, 12, 16]. Despite continuing efforts to identify risk factors for ESFT, its etiology is still unknown.

The aim of this study was to review all cases of ESFT that have been reported to FDA from January 1, 1998, through December 31, 2013, and to assess any possible association with therapeutic products. (FAERS includes therapeutic agents which include drugs and also biologics.) We also conducted an extensive literature search of articles that pertained to the epidemiology of ESFT.

2. Methods

All case reports for drug products that included ESFT from the FDA Adverse Event Reporting System (FAERS) database were analyzed. The FAERS database, including foreign and domestic reports and all age groups, was searched for the time period, January 1, 1998, through December 31, 2013. The following Medical Dictionary for Regulatory Activities (MedDRA) search terms (MedDRA website, http://www.meddra.org/ see [17]) were used to identify any reports of cases with ESFT: Ewing’s sarcoma, Ewing’s sarcoma metastatic, Ewing’s sarcoma recurrent, extraosseous Ewing’s sarcoma, extraosseous Ewing’s sarcoma metastatic, extraosseous Ewing’s sarcoma nonmetastatic, extraosseous Ewing’s sarcoma recurrent, neuroectodermal neoplasm, primitive neuroectodermal tumour, primitive neuroectodermal tumour metastatic, and peripheral primitive neuroectodermal tumour of soft tissue. Cases were stratified by year of occurrence and defined by the reporter as definite, probable, possible, and unlikely in terms of the diagnosis of ES and potential association with drug exposure. Reports of ESFT as a secondary malignancy, as a primary tumor preceding a secondary malignancy, adverse events related to chemotherapy, and other treatments for ESFT and report duplications were excluded. Case reports of medication use pre-ESFT were analyzed by two independent reviewers.

Data Source. This study utilized the FAERS database of adverse event (AE) reports. Since 1969, FDA has maintained this passive surveillance system to detect problems with drugs and biological products used by humans. Manufacturers are required by US law to report AEs associated with their products, and AEs may also be spontaneously reported by health care professionals and consumers. The database contains reports from the US and non-US countries. Reports that the reporter thought to be related to the use of a product are reviewed, coded, and accumulated into an electronic database. The adverse events are codified by MedDRA terminology. This passive surveillance program functions as an early warning system for the detection of serious AEs not identified during the premarket testing or clinical trials. A special feature of this program includes follow-up reports of cases following FDA’s request for further information. Some of the reports in this database may also be found in the published literature.

3. Results

3.1. Overall FAERS Reports Summary

Over the 16-year time period, 134 reports were retrieved with mention of ESFT. After clinical review of the narrative reports 25 cases were identified with a history of medication use prior to ESFT diagnosis, most with a history of ≥18 months. Age range was 5–68 years of age (median 24 years) (Table 1). Many of our cases were outside the adolescent age group.

Primary ESFT after Drug Use () (Table 2). A total of 25 out of 134 reports revealed the use of various suspect drug products with subsequent development of ESFT. Reports were excluded if ESFT occurred as a secondary malignancy, drug adverse events occurred with ESFT therapy, or ESFT occurred as a primary cancer before a secondary cancer occurred that followed drug therapies. The 25 cases of ESFT ranged in age from 4 to 68 years (median 24 years). There was no age information for 4 cases. Thirteen were US cases. Latency to ESFT diagnosis was ≥1 year for 14 cases, <1 year for 5, and unknown for 4. The reported medications included immunosuppressive drugs or drugs used for immune-related disorders (e.g., interferon beta-1, peginterferon alpha-2A and ribavirin, tumor necrosis factor (TNF) blockers, methotrexate, cyclosporine, and azathioprine), isotretinoin, recombinant growth hormone (rGH), and psychotropic medications including antiepileptics (AEDs), atypical antipsychotics, and psychostimulants. Many of the incident cases were confounded by concomitant medications that are labeled for possible carcinogenicity risk.

Twelve cases were treated with immunosuppressive products for a variety of conditions including 3 Crohn’s, 3 multiple sclerosis (MS), 1 renal transplant, 1 rheumatoid arthritis (RA) and 1 each of ankylosing spondylitis, psoriasis vulgaris, chronic hepatitis C genotype 1b, and nephrotic syndrome. Use of more than one immunosuppressant drug was mentioned in 6 of the 12 reports.

Three cases received growth hormone (GH) and were diagnosed with ESFT 18 months to 4 years after beginning therapy. One child was treated with somatropin for microsomia due to neurosecretory GH disorder and a second child was treated for GH deficiency. The third case was a patient with Crohn’s disease who received immunosuppressants and GH (this case is included in the 12 immunosuppressant cases above).

Three cases received other hormonal products, including parathyroid hormone, combined estrogen/progesterone, and etonogestrel implant. The one case treated with recombinant human parathyroid hormone had failed several earlier therapies for osteoporosis. The one case taking combined estrogen/medroxyprogesterone was a menopausal woman who was diagnosed with ESFT 10 months later, and the third case with the etonogestrel implant was a morbidly obese young woman (268 pounds, body mass index (BMI) = 42).

Six cases were treated with psychotropic medications, including 2 with atypical antipsychotics (1 olanzapine for unspecified condition, 1 olanzapine and antiepileptic drugs (AED), clonazepam, for depression), 1 attention deficit hyperactivity disorder (ADHD) drug, methylphenidate, 1 case taking 3 AEDs (ethosuximide, valproic acid, and clobazam), 1 case treated with sodium oxylate for narcolepsy, and 1 case treated with another AED, pregabalin, for neuropathic pain.

There were 2 additional cases that received other medications and then developed ESFT, including 1 young adult treated with isotretinoin for acne and developed ESFT 9 months later and 1 young child treated with atorvastatin for familial hypercholesterolemia.

4. Discussion

The FAERS is a passive surveillance system that collects data on adverse events possibly related to drugs and biologics that are reported to FDA by manufacturers, user facilities, and voluntary reporters, such as health care professionals and consumers. Importantly this system may capture rare and serious events that may not be detected in clinical trials and other studies and may lead to further understanding of possible associations of drugs and other risk factors for various diseases.

While few studies have found any association of exposure to medications with ESFT, our retrospective review of FAERS reports identified 25 cases of ES that followed drug therapy for various conditions. The majority were immunosuppressive agents used to treat autoimmune disorders. Most of the other reported drugs included hormones and psychotropic medications. We also reviewed the published literature to see if our findings might be consistent with other studies and case reports.

While various other malignancies have been reported in association with each of the drugs reported in the FAERS cases, there have been few literature reports of ESFT with the use of these medications. Many of the immunosuppressant drugs and some of the psychotropic and hormonal products are labeled with warnings of increased risk for malignancy or have product labeling for carcinogenicity based on animal studies (Table 3).

While the possible carcinogenic effects would differ for all these products, it may be important that most of the drugs in our case series may affect the hypothalamus and pituitary axis causing growth and neuroendocrine disturbance.

4.1. ESFT Cases following Immunosuppressive Agents

Nine of the 25 (36%) ESFT cases had been previously treated with immunosuppressive agents for autoimmune disorders including Crohn’s disease, MS, RA, psoriasis, and ankylosing spondylitis. Three other cases receiving immunosuppressive therapy included 1 each for renal transplant, chronic hepatitis C, and nephrotic syndrome. Most were older individuals who had received immunosuppressive products two years or more prior to developing ESFT. While many of the case reports did not provide detailed information about duration of therapy and dosage, several reports indicated the use of combination or multimodal therapy with a variety of agents including cytotoxic drugs (e.g., cyclophosphamide, azathioprine, and methotrexate), antibodies and other drug and biologic products for example, interferons, TNF blockers (infliximab, etanercept, and adalimumab), also mesalamine (aminosalicylate, an anti-inflammatory), and 1 case with glucocorticoids.

While ESFT per se has not been reported in association with immunosuppressant drugs, increased exposure to immunosuppressive agents has been found to be related to other cancers [21, 22]. In particular patients receiving higher potency and dosing of therapies for organ transplants have increased cancer risk of non-Hodgkin’s lymphoma (NHL), Kaposi’s sarcoma, nonmelanoma skin cancer, and other malignancies [23, 24]. While the literature highlights the accumulating evidence for elevated cancer risks with some of the immunosuppressant drugs, further studies are needed especially for the newer biologic treatments for immune-mediated inflammatory diseases. It is unclear whether there may be an elevated risk of extraintestinal solid cancers with the newer biologic agents including TNF blockers [25]. There are several limitations in the studies evaluating cancer risk among patients with exposure to immunosuppressive drugs. While no increase in risk of malignancies overall or in cancer subgroups may be found in clinical trials, study patients may not be a representative sample population and the length of follow-up might not be sufficiently long for malignancies to occur [26]. It is not always clear if it is the underlying autoimmune condition, the immunosuppressive therapy (a specific agent, dosage, or number of therapies) [27], or even potentially oncogenic viruses that play a major role in causing these cancers [28]. Several studies have found consistent increased cancer risk for patients with various underlying inflammatory immune diseases, including Crohn’s and RA [29–32]. While the overall cancer incidence and mortality risk are similar to the general population in inflammatory bowel disease, there is an increased cancer risk for Crohn’s and slightly increased risk for RA and psoriasis [21]. Studies have been less consistent in showing increased cancer risk associated with MS [33–35] and ankylosing spondylitis. For ankylosing spondylitis increased cancer risk seems to be associated with radiotherapy [36, 37]. Particularly with newer biologic agents including TNF blockers, further studies are needed to better determine if there is an increased cancer risk with the therapies themselves, with the higher doses, and longer treatments, or whether any increased cancer risk is due to underlying severe disease.

In our case series, most reports had incomplete information with regard to dosage and what additional past therapies had been given for the underlying diseases. While most cases had latency periods over a year, 2 of the MS cases had very short latencies of 3 and 10 months. It seems likely that these may have been misdiagnoses for what was later identified to be ESFT. With ESFT, compared to other malignancies, there is frequently a long period of time after initial symptoms until a diagnosis is made. Studies have shown the mean time to be 19–37 weeks [38–40]. One of the FAERS cases had a history of fibrous dysplasia of the clavicle and then later developed ES at the clavicular site. ES has been reported to mimic fibrous dysplasia [41–43].

From a regulatory perspective, FDA classifies carcinogenic risk of drugs and biologics based on their mechanism of action and hazard identification from in vivo and in vitro nonclinical assays [43]. In our series of 25 FAERS cases, 8 had received immunosuppressive products which are labeled with Box Warnings for carcinogenicity and the other 4 reports included immunosuppressants interferon beta-1a (2 FAERS reports), peginterferon alfa-2b (1 FAERS report), and natalizumab (1 FAERS report) which are not labeled for carcinogenicity. Three of these have not undergone carcinogenicity testing. Despite the clear association between immunosuppressant drugs and increased risk of cancer, many products may fail to predict an increased risk in the preclinical studies [44]. Identification of cancer risk with postmarketing pharmacovigilance is crucial. With regard to ESFT, not only is it a rare malignancy, but unlike other bone cancers such as osteosarcoma, there is no animal model.

We also conducted an extensive literature search for additional cases of ESFT reported with underlying autoimmune disorders or immunosuppressive therapy. In addition to the one renal transplant case in our series which was a case report by Balakrishnan et al. [18], we found three additional ESFT cases following renal transplant in the literature, 1 in a 34-year-old female with vaginal PNET [45], a 15-year-old female with PNET of uterus 9 years after renal transplant for end stage renal disease [46], and a case of unknown age with ESFT of the sacrum following renal transplant [47]. A higher risk of developing malignancy in transplant recipients has been reported [48]. No additional published cases of ESFT associated with other autoimmune disorders or immunosuppressant agents were found.

4.2. ESFT Cases following Hormonal Drugs

There were three reports of ESFT following GH therapy, including two with GH deficiency and an additional case with Crohn’s disease who received both GH and immunosuppressants (included in the 12 immunosuppressant drug reports above). It remains unclear if GH is a carcinogen. Studies have conflicting results regarding any association with GH and cancer. A French population-based cohort study, The French Safety and Appropriateness of Growth Hormone treatments in Europe (SAGhE), of patients treated with recombinant GH reported an increased risk of bone cancers ( cases observed versus 0.6 expected; SMR 5.00; 95% CI, 1.01–14.63), both osteosarcoma (2 cases, statistically nonsignificant) and Ewing sarcoma (1 case, statistically significant) [49]. The selected population for the study included low risk patients who were treated for conditions of idiopathic isolated GH deficiency, idiopathic short stature, short stature in children born short for gestational age, or isolated GH deficiency associated with a minor craniofacial malformation, such as cleft lip. Patients in the middle risk category with pediatric syndromes such as Turner and Noonan syndrome were excluded. The authors of the study thought the elevated bone cancer risk was biologically plausible as bone cancers occur during rapid bone growth of puberty that relate to the insulin-like growth factor 1 (IGF-1) system. It is known that GH and IGF-I do have mitogenic and antiapoptotic activity and that there is a theoretical risk that GH treatment may be associated with cancer [50]. However, interpretation of the study results is limited by the select patient population, the relatively short-term follow-up, and lack of information on the administered GH doses. Other subsequent studies did not demonstrate any increased cancer risks [51–56]. Currently, while GH does not appear to increase the risk for new malignancy in children without known risk factors, an increased risk of a second neoplasm, mostly intracranial tumors in those with prior radiation, has been reported in childhood cancer survivors treated with GH compared with those not treated [51, 55, 57] and this is in the labeling for GH products. Overall, there remain concerns about the possibility of delayed posttreatment effects of heightened GH and IGF-1 on cancer risk. It is unknown if GH treatment may increase the risk of cancer in patients with short stature. Further ongoing surveillance and longer-term studies are needed.

ESFT is thought to be of neural origin and while neurogenic cancers such as neuroblastoma have been reported after GH, we could find no additional literature reports of ESFT following GH. In our ESFT cases one might wonder about the possible risk factor for cancer: is it the GH or is it related to the underlying growth disorder itself?

The other therapeutic hormonal drugs prior to ESFT diagnosis in our series included progestin, combined estrogen/progestin, and parathyroid hormone in nonadolescent females. Our literature review revealed one case report of ES in a young woman four months following abortion [58]. Her only reported drug exposure was four years of oral contraceptive (levonorgestrel 0.05 mg and ethinylestradiol 0.03 mg). (Pregnancy itself leads to decreased circulating GH and slightly increased IGF.)

4.3. Growth and Neuroendocrine Effects of the Drugs Used Pre-ESFT

It is of interest that 16 of the 25 FAERS reports involved various drugs that all have an influence or effect on the hypothalamic-pituitary axis. In particular interferons may be associated growth suppression. Some studies showed that immunosuppressive agents, such as TNF blockers (e.g., infliximab), can also affect the hypothalamic-pituitary-adrenal axis [59]. One of the cases treated with a TNF blocker had also received growth hormone. Many of the psychotropic drugs cause hyperprolactinemia. Antipsychotic drugs may be prone to causing hyperprolactinemia [60] and patients treated with psychostimulants may experience slowing of growth or growth retardation. Small transient decreases in serum IGF-1 may occur early in the treatment of patients with methylphenidate. This is less common in females [61]. Seizure medications, especially valproic acid and ethosuximide, have been known to be associated with hyperandrogenism, menstrual disorders, and polycystic ovary syndrome [62]. Isotretinoin has an effect on the pituitary adrenal axis with mild suppression of pituitary hormones. While long-term studies are needed, Karadag et al. [63] found that isotretinoin appeared to have a negative influence on the GH/IGF-1 axis, with a significant decrease in IGF-1 and IGFBP3 levels after 3 months of isotretinoin treatment. Also, steroids used to treat Crohn’s may cause suppression of the HPA axis.

Epilepsy itself [62] has sex-specific effects on hormone levels and reproductive function. Women with seizures have hypothalamic disorders, amenorrhea and reproductive/endocrine disorders, and ovarian cysts [64, 65].

4.4. ESFT Cases following Psychotropic Drugs

The other category of pre-ESFT therapies included psychotropic drugs. There was only 1 case of each therapy in this category. Currently, most antipsychotic drugs are not considered to increase the risk of cancer [66]. One product, clozapine, has a separate status given that this molecule shows antiproliferative effects implied in agranulocytosis as well as a potential increased risk for leukemia [67].

4.5. Literature Review of Studies and Case Reports of ESFT

Few studies have closely examined drug exposures in children who later develop ESFT. Past registry, case-control studies and case series that collected data on medication use [9, 10, 12, 16] have not consistently identified any specific drug therapy as a risk factor for ESFT (see Table 4). Due to the rarity of ESFT, many studies examining possible risk factors lack the statistical power to definitely prove or disprove any association with medication exposures, underlying diseases or genetic disorders. Several studies and literature reports have found a wide array of different medical conditions, anomalies, and even genetic syndromes in patients who developed ESFT (Table 4). More than one study reported congenital genitourinary and renal anomalies (e.g., cryptorchidism, duplication of ureters and collecting system, and inguinal hernias) and musculoskeletal and spinal anomalies (e.g., cervical ribs, spina bifida, and myelomeningocele) [9, 12–15, 20, 68, 69]. It is of interest that many of these conditions are known to be associated with growth and neuroendocrine dysfunction. Our literature review found reports of ESFT in patients with other genetic syndromes including 4 articles with 5 cases with Down syndrome [20, 70–72], 1 case with chromosome 18q-deletion syndrome [73], and 2 cases with osteogenesis imperfecta [14]. While these syndromes are not uncommon and it might be expected that ESFT would occur, it is of interest that all these syndromes are known to be associated with short stature with abnormal pubertal growth and GH deficiency or pituitary dysfunction. Unlike osteosarcoma there has been no consistent association with tall stature or pubertal bone growth in patients with ESFT [10, 16, 19, 74]. Perhaps it is the hormonal changes and interference with growth aspects of puberty that are awry in the development of ESFT.

While our FAERS reports were submitted to FDA in association with drug use, the reported therapies were used to treat autoimmune disorders and childhood conditions that, especially if severe, might lead to growth and/or endocrine disturbance. Crohn’s disease, renal failure (especially posttransplant), psychoses, and epilepsy [62, 64] may all cause or be associated with hyperprolactinemia, growth disturbance, and/or pituitary dysfunction during childhood and adolescence. Thus, these cases might also support that there is an underlying endocrine disturbance in patients with ESFT. Also, the various inflammatory conditions that were treated with immunosuppressants in our FAERS case series may also affect bone health (e.g., RA, Crohn’s, and MS) and alter pubertal development. Mood disorders such as anxiety, bipolar disorder, insomnia, and fibromyalgia also involve the HPA axis and GH deficiency is associated with high cholesterolemia, osteoporosis, and short stature.

4.6. Limitations

The observation of a small number of cases of an uncommon cancer occurring in association with certain exposures does not provide evidence of any causal link. This study using the FDA database has several limitations including reporting biases for cases from manufacturers as well as health care professionals and consumers. FAERS cases may be reported to FDA from postmarket surveillance studies with incomplete enrollment and reporting is dependent upon physician investigator compliance with submitting forms consistently and accurately, and whether the reported disease is related or unrelated to the therapy is subjective. Submitted reports may lack important information on the underlying disease, comorbid conditions, and prior therapies. These reports do not provide histopathologic confirmation of the cancer diagnosis. Another limitation of this study is that it is a retrospective analysis. However, epidemiological studies on patient populations also have limited value because of the long latency period for most cancers and because most studies lack sensitivity. Most studies approach bone cancers as a group without breakdown into subtypes of osteosarcoma and ESFT which are thought to have very different etiologies. Nonetheless, FAERS is the largest postmarketing drug safety database in the world maintained by a single country, containing more than 9 million reports of “drug-related” (but not necessarily causal) adverse event reports since 1969. Because of its potential comprehensiveness in capturing rare drug-associated adverse events from all over the world, the FAERS data may be useful in generating hypotheses relating to possible causes of a specific rare cancer, which later if warranted may be tested in formal and more rigorous epidemiological studies.

5. Conclusions

ESFT is known for its striking unimodal incident peak during puberty and few risk factors have been identified as to its etiology. In this present study we found ESFT cases following the use of immunosuppressant agents as well as hormonal medications. These medications as well as the reported underlying immune disorders and neuroendocrine conditions are associated with abnormal growth and hormonal disturbance. These findings may provide insight as to why this cancer has a peak incidence during adolescence. Perhaps the neuroendocrine abnormalities might even be linked to a common gene. Formal epidemiological or clinical studies should be conducted to further evaluate any possible role of neuroendocrine disturbances with these underlying conditions and drugs in the development of ESFT.

Disclosure

All authors are government employees of the Food and Drug Administration, HHS.

Conflict of Interests

The authors have no conflict of interests to report.

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Copyright © 2015 Judith U. Cope et al. 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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