Renal Dysfunction is a Risk Factor of Death after Gastric Endoscopic Submucosal Dissection in Elderly Patients Aged ≥80 Years

Okimoto, Kenichiro; Arai, Makoto; Ishigami, Hideaki; Taida, Takashi; Saito, Keiko; Maruoka, Daisuke; Matsumura, Tomoaki; Nakagawa, Tomoo; Katsuno, Tatsuro; Kato, Naoya

doi:https://doi.org/10.1155/2019/7145182

Canadian Journal of Gastroenterology and Hepatology

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Abstract Introduction Methods Results Discussion Abbreviations Data Availability Ethical Approval Consent Conflicts of Interest Authors’ Contributions Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2019 | Article ID 7145182 | https://doi.org/10.1155/2019/7145182

Renal Dysfunction is a Risk Factor of Death after Gastric Endoscopic Submucosal Dissection in Elderly Patients Aged ≥80 Years

Kenichiro Okimoto,¹Makoto Arai,¹Hideaki Ishigami,¹Takashi Taida,¹Keiko Saito,¹Daisuke Maruoka,¹Tomoaki Matsumura,¹Tomoo Nakagawa,¹Tatsuro Katsuno,¹and Naoya Kato¹

Academic Editor: Michel Kahaleh

Received23 May 2018

Revised18 Nov 2018

Accepted22 Jul 2019

Published09 Sept 2019

Abstract

Introduction. Endoscopic submucosal dissection (ESD) for early gastric cancer (EGC) is well accepted. However, its adaptation for elderly patients is unclear. This study aimed to investigate the prognosis and long-term outcomes of ESD for EGC in elderly patients aged ≥80 years by comparing their findings to the findings of patients aged <80 years. Materials and Methods. The study included 533 patients (632 lesions). The patients were divided into an elderly group (age, ≥80 years; 108 patients; 128 lesions; mean age, 83.4 ± 2.7 years) and a nonelderly group (age, <80 years; 425 patients; 504 lesions; mean age, 69.6 ± 7.9 years). We compared patient and lesion characteristics, overall survival (OS), and disease-specific survival (DSS) between the 2 groups retrospectively. Multivariate analysis was performed to clarify the risk factors of death after ESD. Results. The rate of curative resection and adverse events was not significantly different between the groups. The mean survival time periods with regard to OS/DSS in the elderly and nonelderly groups were 75.8 ± 5.9 and 122.8 ± 2.6 months ()/120.0 ± 3.0 and 136.4 ± 0.6 months (not significant), respectively. In the elderly group, eGFR <30 ml/min/1.73 m² was an independent risk factor of death (hazard ratio = 5.32; 95% confidence interval = 1.39–20.5; ). Conclusion. ESD for EGC can be performed safely and can achieve high curability with good prognosis in elderly patients aged ≥80 years. After ESD, close attention should be paid to elderly patients with severe chronic kidney disease.

1. Introduction

Gastric cancer is one of the most common cancers globally and is the second most common cause of cancer-related death [1]. Among the various treatment options for early gastric cancer (EGC), gastric endoscopic submucosal dissection (ESD) is well accepted because it is less invasive than conventional surgery [2–5]. The guidelines of ESD for EGC have been established [6]. Good short- and long-term outcomes of gastric ESD have been reported when the procedure was conducted following the guidelines [7–13].

Recently, the life expectancies of male and female patients have been reported to be 79 and 86 years in Japan [14], indicating that the aging society is rapidly growing. Elderly patients tend to have several comorbidities, and their general condition is occasionally poor, indicating that minimally invasive treatments for EGC, such as ESD, in these patients are important. However, we are sometimes distressed by the adaptation of gastric ESD for elderly patients when their clinical conditions are considered. Although several reports have mentioned the outcomes of gastric ESD in elderly patients [15–20], there is little consensus on the indication of gastric ESD and the prognosis in elderly patients.

The aim of this study was to investigate the prognosis and long-term outcomes of gastric ESD in elderly patients aged ≥80 years by comparing their findings to the findings of patients aged <80 years.

2. Methods

2.1. Study Design and Patients

This retrospective study was conducted in Chiba University Hospital, Japan. From May 2005 to September 2016, 533 patients (632 lesions) who underwent gastric ESD for EGC were enrolled. We classified patients aged ≥80 years into an elderly group and those aged <80 years into a nonelderly group according to the previous report [21]. There were 108 patients (128 lesions) in the elderly group and 425 patients (504 lesions) in the nonelderly group. We compared patient and lesion characteristics, as well as long-term outcomes between the 2 groups. Curability was assessed, and intragroup comparisons were performed. The study protocol was approved by the Institutional Review Board of Chiba University and was registered (Clinical Registration Number: UMIN000024856).

2.2. Indication of Gastric ESD

We performed ESD for EGC that was judged as the absolute or expanded indication before ESD, according to the Japanese gastric cancer treatment guidelines 2010 (ver. 3) [6]. Patients with ECOG performance status (PS) 0 or 1 were treated. When the patients had cancers other than EGC, we consulted with doctors from specific fields, and only if their prognosis was considered acceptable on the condition that curative ESD was achieved, we performed ESD. When patients had other comorbidities, we held discussions among individuals from our ESD treatment team, as well as other specific fields, and physicians closely judged the adaptation of gastric ESD.

2.3. Patient and Lesion Characteristics

We collected patient clinical data, including age, sex, body mass index (BMI), preoperative estimated glomerular filtration rate (eGFR), and comorbidities (cardiovascular disease (CVD), history of cerebrovascular disease, and cancers other than gastric cancer). Adverse events of ESD were also assessed. The locations of the lesions in the stomach were classified into upper, middle, or lower. Tumor size, pathological findings, and depth of invasion were examined along with the Japanese gastric cancer treatment guidelines [6]. Macroscopic type was classified into elevated, flat/depressed, or mixed (combination of the previous 2 types), as previously reported [20]. We compared these factors between the 2 groups.

2.4. Curative Evaluation of the Resected Specimens

Curability was examined according to Japanese gastric cancer treatment guidelines [6]. Curative resection (CR) was determined when the resected specimen with negative horizontal and vertical margins and without lymphovascular invasion met any of the following 4 criteria: (1) differentiated-type intramucosal adenocarcinoma without ulcerative findings regardless of the tumor size; (2) differentiated-type intramucosal adenocarcinoma with ulcerative findings and tumor size ≤30 mm; (3) differentiated-type shallow submucosal (SM1) carcinoma and tumor size ≤30 mm; (4) undifferentiated adenocarcinoma without ulcerative findings and tumor size ≤20 mm.

Non-CR was determined when the resected specimen did not meet any of the 4 CR criteria or was margin (horizontal or vertical) positive.

2.5. Long-Term Outcomes

We collected data regarding long-term outcomes. For patients who visited our hospital regularly, we obtained data from the databases in our hospital. For patients who did not visit our hospital regularly, we contacted the patients at their home or obtained information from their physician. We assessed overall survival (OS) and disease-specific survival (DSS) with regard to gastric cancer for each group and compared OS and DSS between the elderly and nonelderly groups. Survival rates between patients whose eGFR was <30 ml/min/1.73 m² (CKD stage G4 and G5 according to Japanese CKD guidelines [22]) and other patients in each group were analyzed. Also, survival rates between patients whose BMI was <22 kg/m² (BMI 22 kg/m² is Japanese ideal BMI [23]) and other patients in each group were analyzed. Additionally, univariate and multivariate analyses in each group as well as overall assessments between patients who died and those who were still alive during the observation period were performed.

2.6. Statistical Analysis

Patient and lesion characteristics, curability, adverse events, and items with regard to long-term outcomes were compared between the elderly and nonelderly groups using Fisher’s exact test, the chi-square test, or unpaired t-tests. OS, DSS, and the survival rate were investigated using the Kaplan–Meier method and were compared using the log-rank test. OS and the survival rate were calculated from the first ESD to the date of death or latest confirmation of patient survival. DSS was calculated from the first ESD to the date of death caused by gastric cancer or latest confirmation of patient survival. For calculating DSS, patients who died from conditions other than gastric cancer were excluded. Univariate and multivariate analyses were performed with cox-regression analysis. Variables with in univariate analysis were subjected to multivariate analysis. All statistical analyses were performed using SPSS version 22.0 (SPSS Inc., Chicago, IL, USA). A value <0.05 was considered statistically significant.

3. Results

3.1. Patient and Lesion Characteristics

Patient characteristics are shown in Table 1. The mean ages of the patients in the elderly and nonelderly groups were 83.4 ± 2.7 and 69.6 ± 7.9 years, respectively. There were no significant differences with regard to sex, BMI, and ECOG-PS between the 2 groups. Preoperative eGFR (ml/min/1.73 m²) was significantly lower in the elderly group than in the nonelderly group (57.6 ± 16.8 vs. 69.4 ± 18.9, , unpaired t-test). The percentage of patients who had already started using anticoagulants and/or antiplatelet drugs was significantly higher in the elderly group than in the nonelderly group (27.8% vs. 16.0%, , chi-square test). With regard to comorbidities, the number of patients with hypertension was higher in the elderly group than in the nonelderly group (50.0% vs. 38.4%, , chi-square test).

Table 2 shows the characteristics of the lesions. There were no significant differences with regard to macroscopic type, location, histological type, tumor depth, tumor size, and lymphatic vessel invasion between the elderly and nonelderly groups. On the other hand, the ratio of venous invasion was significantly higher in the elderly group than in the nonelderly group (4.7% vs. 1.0%, , Fisher’s exact test).

3.2. Curability and Adverse Events Related to ESD

The details of curability and adverse events are summarized in Table 3. There were no significant differences with regard to en block resection and CR between the elderly and nonelderly groups. Additional surgical resection was performed in 2 (1.9%) patients from the elderly group and 24 (5.6%) patients from the nonelderly group. In the nonelderly group, 3 out of 24 patients had residual tumor in their resected specimen and no patient had lymphatic metastasis. In elderly group, one patients had lymphatic metastasis as well as tumor recurrence in residual specimen (details of this patient are shown in Supplementary table 1). The rates of adverse events related to ESD, such as postoperative bleeding, perforation, aspiration pneumonia, and delirium, were not significantly different between the 2 groups. There were no deaths related to adverse events, and every adverse event was reversible.

3.3. Long-Term Outcomes of ESD

The long-term outcomes of ESD are shown in Table 4. The mean observation periods were 26.9 ± 23.2 and 36.4 ± 29.6 months in the elderly and nonelderly groups, respectively (, unpaired t-test.). The rate of the patients with ≥3 years follow-up was 28.7% and 41.9% (31 and 178 patients) in the elderly and nonelderly groups, respectively. The rate of the patients with ≥5 years follow-up period was 7.4% and 20.0% (8 and 85 patients) in the elderly and nonelderly groups, respectively.

Each group had 1 gastric cancer death. Within the observation period, 13 (12.0%) and 28 (6.6%) patients in the elderly and nonelderly groups, respectively, died from conditions other than gastric cancer. The mean time periods from ESD to death from conditions other than gastric cancer were 30.2 ± 16.6 and 26.8 ± 17.8 months in the elderly and nonelderly groups, respectively. The rate of patients who died from renal dysfunction was significantly higher in the elderly group than in the nonelderly group. OS in each group is shown in Figure 1(a). The mean survival time periods were 75.8 ± 5.9 and 122.8 ± 2.6 months in the elderly and nonelderly groups, respectively (, log-rank test). DSS is shown in Figure 1(b). The mean survival time periods were 98.0 ± 2.0 and 136.4 ± 0.6 months in the elderly and nonelderly groups, respectively (not significant, log-rank test).

(a)

(b)

Figure 1

Comparison of overall survival (OS) and disease-specific survival (DSS) between the elderly and nonelderly groups. (a) Comparison of OS between the elderly and nonelderly groups. The mean survival time periods were 75.8 ± 5.9 and 122.8 ± 2.6 months in the elderly and nonelderly groups, respectively (, log-rank test). (b) Comparison of DSS between the elderly and nonelderly groups. The mean survival time periods were 98.0 ± 2.0 and 136.4 ± 0.6 months in the elderly and nonelderly groups, respectively (not significant, log-rank test).

3.4. Univariate and Multivariate Analyses of Risk Factors

The results of univariate and multivariate analyses of the risk factors of death in all patients (elderly and nonelderly groups) are shown in Table 5. Overall, univariate analysis showed age, sex (male), eGFR <30 ml/min/1.73 m [2], CVD, and use of anticoagulants and/or antiplatelet drugs were significantly associated with the death after ESD. On the other hand, multivariate analysis showed that age and eGFR <30 ml/min/1.73 m [2] were independent risk factors of the death after ESD. In the nonelderly group, multivariate analysis showed BMI (<22 kg/m²) and eGFR <30 ml/min/1.73 m² were risk factors of the death after ESD. In the elderly group, multivariate analysis showed that eGFR <30 ml/min/1.73 m [2] was an independent risk factor of death (hazard ratio = 5.32; 95% confidence interval = 1.39–20.5; ). There were 7 (3 died) and 13 (3 died) patients whose eGFR was <30 ml/min/1.73 m² in the elderly and nonelderly groups, respectively. In the elderly group, of these 3 patients whose eGFR was <30 ml/min/1.73 m [2], 1 patient died from renal failure while cause of the death of the other 2 patients were unclear. In the nonelderly group, of these 3 patients whose eGFR was <30 ml/min/1.73 m [2], 1 patient died from multiple organ failure and 1 patient died from hepatocellular carcinoma, while cause of the death of the other 1 patient was unclear. The survival rates of the patients whose eGFR was <30 ml/min/1.73 m² and other patients in both groups are shown in Figures 2(a) and 2(b), respectively. The mean survival time periods of the patients whose eGFR was <30 ml/min/1.73 m² and other patients were 36.3 ± 7.9 and 78.2 ± 6.1 months (, log-rank test) in the elderly group and 35.7 ± 5.0 and 124.1 ± 2.6 months (, log-rank test) in the nonelderly group, respectively. There were 39 (2 died) and 141 (15 died) patients whose BMI was <22 kg/m² in the elderly and nonelderly groups, respectively. The survival rates of the patients whose BMI was <22 kg/m² and other patients in both groups are shown in Supplementary figure 1. The mean survival time periods of the patients whose BMI was <22 kg/m² and other patients were 93.3 ± 4.5 and 62.8 ± 5.8 months (not significant, log-rank test) in the elderly group and 91.8 ± 4.1 and 115.2 ± 2.2 months (, log-rank test) in the nonelderly group, respectively.

(a)

(b)

Figure 2

Comparison of the survival rate between patients whose estimated glomerular filtration rate (eGFR) was <30 ml/min/1.73 m² and other patients in the elderly and nonelderly groups. (a) Elderly group. The mean survival time periods were 36.3 ± 7.9 and 78.2 ± 6.1 months among patients whose eGFR was <30 ml/min/1.73 m² and among other patients, respectively (, log-rank test). (b) Nonelderly group. The mean survival time periods were 35.7 ± 5.0 and 124.1 ± 2.6 months among patients whose eGFR was <30 ml/min/1.73 m² and among other patients, respectively (, log-rank test).

3.5. Characteristics of the Patients Who Died from Gastric Cancer and Their Lesions

The details of the patients who died from gastric cancer and their lesions are shown in Supplementary table 1. As previously described, in each group, 1 patient died from gastric cancer. One patient was a 74-year-old man with non-CR. He refused to undergo additional treatment and died 35 months after ESD. The other patient was an 80-year-old man with non-CR. He had myelodysplastic syndrome (MDS). Gastrectomy and lymphadenectomy were performed when local recurrence was detected 24 months after ESD. The pathology showed lymph node metastasis. However, adjuvant chemotherapy could not be performed because of MDS. He died 35 months after ESD.

4. Discussion

Some previous studies have analyzed OS and the risk factors of death among elderly patients with EGC after ESD [18–20]. Sumiyoshi et al. reported that the 5-year survival rates of elderly patients with EGC who underwent ESD after CR and non-CR with and without additional surgical resection were 84.6%, 73.3%, and 58.8%, respectively [18]. Yoshifuku et al. reported that during the follow-up period after ESD for EGC, the frequency of death was significantly higher in patients with low- and high-risk comorbidities than in those with no comorbidities [19]. However, to the best of our knowledge, no reports have examined OS in elderly patients with EGC after ESD with a focus on not only eGFR but also CKD staging, and therefore, the present study is novel. The survival rate was significantly shorter among patients whose eGFR was <30 ml/min/1.73 m² than among other patients in both groups. Furthermore, eGFR <30 ml/min/1.73 m² was an independent risk factor of death in the elderly group. Imai et al. reported that eGFR declines in accordance with aging [24]. Patients with CKD have a high risk of hospitalization for pneumonia, sepsis, and bacteremia [25]. Especially, patients with severe CKD have more risk of cancer development [26]. Furthermore, CKD stages G4 and G5 (eGFR <30 ml/min/1.73 m²) are more frequently associated with terminal renal dysfunction and mortality, as well as the incidence of CVD events, when compared to the incidence of these events for other stages of CKD [27, 28]. Special care should be taken when following up elderly patients with eGFR <30 ml/min/1.73 m² who have a high risk of death during observation.

With regard to OS, the mean survival time was 75.8 ± 5.9 months in the elderly group. Considering the average life expectancy of male and female individuals in Japan [14], patients in the elderly group were assumed to live at least as long as the average life expectancy of Japanese individuals. In each of the study groups, 1 patient died from gastric cancer. Consequently, DSS was appropriate in both groups. Tsukuma et al. reported that the cumulative 5-year risk of EGC without any treatment progressing to the advanced stage was 63.0% [29], indicating that EGC generally grows slowly. However, once early gastric cancer grows up to advanced gastric cancer, the 3-year survival rate is 31% for those surgically treated and 0% for those observed conservatively [30]. These reports suggest the importance of ESD for EGC to achieve a high DSS rate.

Sekiguchi et al. reported that the 3-year (54.3% vs. 95.9%) and 5-year OS (54.3% vs. 76.3%) rates were significantly worse in patients with a low prognostic nutritional index among elderly patients who underwent ESD for EGC [20]. In this study, multivariate analysis showed that low BMI was a risk factor of death among nonelderly patients included. Therefore, we should consider a patient’s metabolic status, such as low BMI and low nutritional condition, when performing follow-up after ESD.

The results of this study showed that there were no significant differences with regard to en block resection, CR, and adverse events of ESD between elderly and nonelderly patients. Gastric ESD for EGC in elderly patients aged ≥80 years can achieve high rates of curability and a low risk of adverse events, which are similar to those in nonelderly patients. These results were almost the same as the results of previous reports [16–19]. We could confirm that gastric ESD is a minimally invasive and effective treatment even for elderly patients who are prone to having several comorbidities.

Venous invasion-positive tumors were significantly more common in the elderly group than in the nonelderly group. The presence of papillary or undifferentiated-type adenocarcinoma was reported to be significantly associated with venous involvement [31]. In the elderly group, 3 of 6 venous invasion-positive lesions contained a papillary or undifferentiated adenocarcinoma component. However, only 1 of 5 lesions in the nonelderly group had a papillary adenocarcinoma component, and no lesion had an undifferentiated adenocarcinoma component. This histological difference between the 2 groups might have contributed to the high rate of venous invasion in the elderly group. Of note, for 1 lesion in the elderly group, venous invasion was detected although the tumor was a differentiated-type lesion and the depth was within the intramucosa. When performing gastric ESD for elderly patients, we should consider these factors and pay attention to the explanation provided to patients before ESD, as well as to the postoperative follow-up.

Additional surgical resection was performed in 2 (1.9%) patients in the elderly group and 24 (5.6%) patients in the nonelderly group. Considering the fact that each group had 1 patient who died from gastric cancer, additional surgical resection should not be discouraged even for elderly patients if they consent to the treatment and their general status is appropriate. Sekiguchi et al. developed and validated a risk-scoring model of lymph node metastasis in EGC [32]. This scoring model may be one of the helpful items to judge the adaptation of additional surgical resection.

The present study has some limitations. First, the study design was retrospective, and the study was performed in a single center. Second, the numbers of patients and lesions were relatively small. Third, the follow-up period was relatively short. The mean observation periods in this study were 26.9 and 36.4 months in elderly and nonelderly patients, respectively. These results were rather short compared to those of previously reported (39–41 months) [19, 21]. The risk of cancer recurrence might be estimated lower due to short observation period. In the future, prospective studies with a long-term follow-up are needed to evaluate the long-term outcomes of ESD for EGC in elderly patients.

In conclusion, ESD for EGC can be performed safely and can achieve high curability with a good prognosis in elderly patients aged ≥80 years. After ESD, close attention should be paid when following up elderly patients with severe CKD.

Abbreviations

EGC:	Early gastric cancer
ESD:	Gastric endoscopic submucosal dissection
PS:	Performance status
BMI:	Body mass index
eGFR:	Estimated glomerular filtration rate
CVD:	Cardiovascular disease
CR:	Curative resection
SM:	Submucosa
OS:	Overall survival
CKD:	Chronic kidney disease
DSS:	Disease-specific survival
MDS:	Myelodysplastic syndrome.

Data Availability

All data arising from this study are contained within the manuscript.

Ethical Approval

The study protocol was approved by the Institutional Review Board of Chiba University and was registered (Clinical Registration Number, UMIN000024856).

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964 and later versions. Informed consent to be included in the study, or the equivalent, was obtained from all patients.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Kenichiro Okimoto wrote the paper and performed statistical analysis. Makoto Arai designed research. Hideaki Ishigami, Takashi Taida, Keiko Saito, Daisuke Maruoka, Tomoaki Matsumura, Tomoo Nakagawa, Tatsuro Katsuno, and Naoya Kato analyzed data.

Supplementary Materials

Supplementary table 1: characteristics of the patients who died from gastric cancer and their lesions. Supplementary figure 1: cComparison of the survival rate between patients whose body mass index (BMI) was <22 kg/m² and other patients in the elderly and nonelderly groups. Supplementary figure 1A: elderly group. The mean survival time periods were 93.3 ± 4.5 and 62.8 ± 5.8 months among patients whose BMI was <22 kg/m² and among other patients, respectively (not significant, log-rank test). Supplementary figure 1B: nonelderly group. The mean survival time periods were 91.8 ± 4.1 and 115.2 ± 2.2 months among patients whose BMI was <22 kg/m² and among other patients, respectively (, log-rank test). (Supplementary Materials)

References

J. Ferlay, I. Soerjomataram, R. Dikshit et al., “Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012,” International Journal of Cancer, vol. 136, no. 5, pp. E359–E386, 2015.
View at: Publisher Site | Google Scholar
I. Oda, T. Gotoda, H. Hamanaka et al., “Endoscopic submucosal dissection for early gastric cancer: technical feasibility, operation time and complications from a large consecutive series,” Digestive Endoscopy, vol. 17, no. 1, pp. 54–58, 2005.
View at: Publisher Site | Google Scholar
O. Goto, M. Fujishiro, S. Kodashima, S. Ono, and M. Omata, “Outcomes of endoscopic submucosal dissection for early gastric cancer with special reference to validation for curability criteria,” Endoscopy, vol. 41, no. 2, pp. 118–122, 2009.
View at: Publisher Site | Google Scholar
C. H. Park, H. Lee, D. W. Kim et al., “Clinical safety of endoscopic submucosal dissection compared with surgery in elderly patients with early gastric cancer: a propensity-matched analysis,” Gastrointestinal Endoscopy, vol. 80, no. 4, pp. 599–609, 2014.
View at: Publisher Site | Google Scholar
H. Suzuki, I. Oda, S. Abe et al., “High rate of 5-year survival among patients with early gastric cancer undergoing curative endoscopic submucosal dissection,” Gastric Cancer, vol. 19, no. 1, pp. 198–205, 2016.
View at: Publisher Site | Google Scholar
Japanese Gastric Cancer Association, “Japanese gastric cancer treatment guidelines 2010 (Ver. 3),” Gastric Cancer, vol. 14, no. 2, pp. 113–123, 2011.
View at: Publisher Site | Google Scholar
H. Ono, H. Kondo, T. Gotoda et al., “Endoscopic mucosal resection for treatment of early gastric cancer,” Gut, vol. 48, no. 2, pp. 225–229, 2001.
View at: Publisher Site | Google Scholar
I. Oda, D. Saito, M. Tada et al., “A multicenter retrospective study of endoscopic resection for early gastric cancer,” Gastric Cancer, vol. 9, no. 4, pp. 162–170, 2006.
View at: Publisher Site | Google Scholar
I.-K. Chung, J. H. Lee, S.-H. Lee et al., “Therapeutic outcomes in 1000 cases of endoscopic submucosal dissection for early gastric neoplasms: Korean ESD study Group multicenter study,” Gastrointestinal Endoscopy, vol. 69, no. 7, pp. 1228–1235, 2009.
View at: Publisher Site | Google Scholar
H. Isomoto, S. Shikuwa, N. Yamaguchi et al., “Endoscopic submucosal dissection for early gastric cancer: a large-scale feasibility study,” Gut, vol. 58, no. 3, pp. 333–336, 2009.
View at: Publisher Site | Google Scholar
T. Gotoda, M. Iwasaki, C. Kusano, S. Seewald, and I. Oda, “Endoscopic resection of early gastric cancer treated by guideline and expanded National Cancer Centre criteria,” British Journal of Surgery, vol. 97, no. 6, pp. 868–871, 2010.
View at: Publisher Site | Google Scholar
P. W. Y. Chiu, A. Y. B. Teoh, K. F. To et al., “Endoscopic submucosal dissection (ESD) compared with gastrectomy for treatment of early gastric neoplasia: a retrospective cohort study,” Surgical Endoscopy, vol. 26, no. 12, pp. 3584–3591, 2012.
View at: Publisher Site | Google Scholar
T. Kosaka, M. Endo, Y. Toya et al., “Long-term outcomes of endoscopic submucosal dissection for early gastric cancer: a single-center retrospective study,” Digestive Endoscopy, vol. 26, no. 2, pp. 183–191, 2014.
View at: Publisher Site | Google Scholar
Ministry of Internal Affairs and Communications Statistics Bureau, “Average life expectancy of Japanese population,” April 2016, http://www.stat.go.jp/data/nihon/02.htm.
View at: Google Scholar
N. Kakushima, M. Fujishiro, S. Kodashima et al., “Technical feasibility of endoscopic submucosal dissection for gastric neoplasms in the elderly Japanese population,” Journal of Gastroenterology and Hepatology, vol. 22, no. 3, pp. 311–314, 2007.
View at: Publisher Site | Google Scholar
H. Isomoto, K. Ohnita, N. Yamaguchi et al., “Clinical outcomes of endoscopic submucosal dissection in elderly patients with early gastric cancer,” European Journal of Gastroenterology and Hepatology, vol. 22, no. 3, pp. 311–317, 2010.
View at: Publisher Site | Google Scholar
T. Toyokawa, I. Fujita, T. Morikawa et al., “Clinical outcomes of ESD for early gastric neoplasms in elderly patients,” European Journal of Clinical Investigation, vol. 41, no. 5, pp. 474–478, 2011.
View at: Publisher Site | Google Scholar
T. Sumiyoshi, H. Kondo, R. Fujii et al., “Short- and long-term outcomes of endoscopic submucosal dissection for early gastric cancer in elderly patients aged 75 years and older,” Gastric Cancer, vol. 20, no. 3, pp. 489–495, 2017.
View at: Publisher Site | Google Scholar
Y. Yoshifuku, S. Oka, S. Tanaka et al., “Long-term prognosis after endoscopic submucosal dissection for early gastric cancer in super-elderly patients,” Surgical Endoscopy, vol. 30, no. 10, pp. 4321–4329, 2016.
View at: Publisher Site | Google Scholar
M. Sekiguchi, I. Oda, H. Suzuki et al., “Clinical outcomes and prognostic factors in gastric cancer patients aged ≥85 years undergoing endoscopic submucosal dissection,” Gastrointestinal Endoscopy, vol. 85, no. 5, pp. 963–972, 2017.
View at: Publisher Site | Google Scholar
N. Abe, T. Gotoda, T. Hirasawa et al., “Multicenter study of the long-term outcomes of endoscopic submucosal dissection for early gastric cancer in patients 80 years of age or older,” Gastric Cancer, vol. 15, no. 1, pp. 70–75, 2012.
View at: Publisher Site | Google Scholar
Japanese Society of Nephrology, Evidence-based Clinical Practice Guideline for CKD 2013, Japanese Society of Nephrology, Tokyo, Japan, 2014.
Y. Matsuzawa, K. Tokunaga, K. Kotani, Y. Keno, T. Kobayashi, and S. Tarui, “Simple estimation of ideal body weight from body mass index with the lowest morbidity,” Diabetes Research and Clinical Practice, vol. 10, no. 1, pp. S159–S164, 1990.
View at: Publisher Site | Google Scholar
E. Imai, M. Horio, K. Yamagata et al., “Slower decline of glomerular filtration rate in the Japanese general population: a longitudinal 10-year follow-up study,” Hypertension Research, vol. 31, no. 3, pp. 433–441, 2008.
View at: Publisher Site | Google Scholar
A. J. Collins, R. Foley, C. Herzog et al., “Excerpts from the United States renal data system 2007 annual data report,” American Journal of Kidney Diseases, vol. 51, no. 1, pp. S1–S320, 2008.
View at: Publisher Site | Google Scholar
P. Maisonneuve, L. Agodoa, R. Gellert et al., “Cancer in patients on dialysis for end-stage renal disease: an international collaborative study,” The Lancet, vol. 354, no. 9173, pp. 93–99, 1999.
View at: Publisher Site | Google Scholar
K. Nakamura, T. Okamura, T. Hayakawa et al., “Chronic kidney disease is a risk factor for cardiovascular death in a community-based population in Japan,” Circulation Journal, vol. 70, no. 8, pp. 954–959, 2006.
View at: Publisher Site | Google Scholar
R. Okubo, H. Kai, M. Kondo et al., “Health-related quality of life and prognosis in patients with chronic kidney disease: a 3-year follow-up study,” Clinical and Experimental Nephrology, vol. 18, no. 5, pp. 697–703, 2014.
View at: Publisher Site | Google Scholar
H. Tsukuma, A. Oshima, H. Narahara, and T. Morii, “Natural history of early gastric cancer: a non-concurrent, long term, follow up study,” Gut, vol. 47, no. 5, pp. 618–621, 2000.
View at: Publisher Site | Google Scholar
I. Matsushita, H. Hanai, M. Kajimura et al., “Should gastric cancer patients more than 80 Years of age undergo surgery?” Journal of Clinical Gastroenterology, vol. 35, no. 1, pp. 29–34, 2002.
View at: Publisher Site | Google Scholar
M. Sekiguchi, S. Sekine, I. Oda et al., “Risk factors for lymphatic and venous involvement in endoscopically resected gastric cancer,” Journal of Gastroenterology, vol. 48, no. 6, pp. 706–712, 2013.
View at: Publisher Site | Google Scholar
M. Sekiguchi, I. Oda, H. Taniguchi et al., “Risk stratification and predictive risk-scoring model for lymph node metastasis in early gastric cancer,” Journal of Gastroenterology, vol. 51, no. 10, pp. 961–970, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2019 Kenichiro Okimoto 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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