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Clinical Trial
. 2014 Sep;105(9):1176-81.
doi: 10.1111/cas.12473. Epub 2014 Sep 6.

Multicenter retrospective analysis of systemic chemotherapy for advanced neuroendocrine carcinoma of the digestive system

Affiliations
Clinical Trial

Multicenter retrospective analysis of systemic chemotherapy for advanced neuroendocrine carcinoma of the digestive system

Tomohiro Yamaguchi et al. Cancer Sci. 2014 Sep.

Abstract

This study analyzed outcomes of systemic chemotherapy for advanced neuroendocrine carcinoma (NEC) of the digestive system. Clinical data from 258 patients with unresectable or recurrent NEC of the gastrointestinal tract (GI) or hepato-biliary-pancreatic system (HBP), who received chemotherapy, were collected from 23 Japanese institutions and analyzed retrospectively. Patients had primary sites in the esophagus (n = 85), stomach (n = 70), small bowel (n = 6), colorectum (n = 31), hepato-biliary system (n = 31) and pancreas (n = 31). Median overall survival (OS) was 13.4 months the esophagus, 13.3 months for the stomach, 29.7 months for the small bowel, 7.6 months for the colorectum, 7.9 months for the hepato-biliary system and 8.5 months for the pancreas. Irinotecan plus cisplatin (IP) and etoposide plus cisplatin (EP) were most commonly selected for GI-NEC and HBP-NEC. For patients treated with IP/EP (n = 160/46), the response rate was 50/28% and median OS was 13.0/7.3 months. Multivariate analysis among patients treated with IP or EP showed that the primary site (GI vs HBP; hazard ratio [HR] 0.58, 95% confidence interval [CI] 0.35-0.97) and baseline serum lactate dehydrogenase levels (not elevated vs elevated; HR 0.65, 95% CI 0.46-0.94) were independent prognostic factors for OS, while the efficacy of IP was slightly better than for EP (HR 0.80, 95% CI 0.48-1.33; P = 0.389). IP and EP are the most common treatment regimens for NEC of the digestive system. HBP primary sites and elevated lactate dehydrogenase levels are unfavorable prognostic factors for survival. A randomized controlled trial is required to establish the appropriate chemotherapy regimen for advanced NEC of the digestive system. This study was registered at UMIN as trial number 000005176.

Keywords: Cisplatin; digestive system; etoposide; irinotecan; neuroendocrine carcinoma.

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Figures

Fig 1
Fig 1
Flow chart of the study population. CRT, chemoradiotherapy; Cx, chemotherapy; EP, etoposide plus cisplatin; IP, irinotecan plus cisplatin; n, number; NEC, neuroendocrine carcinoma; RT, radiotherapy.
Fig 2
Fig 2
Kaplan–Meier curves for overall survival according to the primary site. CR, colorectum; Eso, esophagus; HB, hepato-biliary system; OS, overall survival; P, pancreas; SB, small bowel; Stm, stomach.
Fig 3
Fig 3
Kaplan–Meier curves for overall survival according to histology. MEEC, mixed endocrine-exocrine carcinoma; NEC, neuroendocrine carcinoma; OS, overall survival; PDNEC, poorly differentiated neuroendocrine carcinoma; RR, response rate; SCC, small cell carcinoma.

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