Chemotherapy with 5-fluorouracil, cisplatin and streptozocin for neuroendocrine tumours

N. C. Turner, S. J. Strauss, D. Sarker, R. Gillmore, A. Kirkwood, A. Hackshaw, A. Papadopoulou, J. Bell, I. Kayani, C. Toumpanakis, F. Grillo, A. Mayer, D. Hochhauser, R. H. Begent, M. E. Caplin, T. Meyer

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153 Citations (Scopus)


BACKGROUND: The role of chemotherapy for neuroendocrine tumours remains controversial and there is no standard regimen. METHODS: We report the outcome for a consecutive series of chemonaive patients with metastatic or locally advanced neuroendocrine tumours treated with a combination of 5-fluorouracil (500 mgm(-2)), cisplatin (70 mgm(-2)) and streptozocin (1000 mgm(-2)) (FCiSt) administered three weekly for up to six cycles. Patients were assessed for radiological response, toxicity and survival. RESULTS: In the 79 patients assessable for response, treatment with FCiSt was associated with an overall response rate of 33% (38% for pancreatic primary sites and 25% for non-pancreatic primary sites). Stable disease occurred in a further 51%, with progression in 16%. The median time to progression was 9.1 months and median overall survival was 31.5 months. The most common grade 3-4 toxicity was neutropaenia (28% patients) but grade 3-4 infection was rare (7%). The most frequent non-haematological grade 3-4 toxicity was nausea and vomiting (17%). Prognostic factors included Ki-67, mitotic index, grade and chromogranin A, whereas response to chemotherapy was predicted by mitotic index, grade and a-fetoprotein. CONCLUSION: FCiSt is an effective regimen for neuroendocrine tumours with an acceptable toxicity profile. Grade and mitotic index are the best predictors of response. British Journal of Cancer (2010) 102, 1106-1112. doi:10.1038/sj.bjc.6605618 Published online 16 March 2010 (C) 2010 Cancer Research UK
Original languageEnglish
Pages (from-to)1106 - 1112
Number of pages7
JournalBJC: British Journal of Cancer
Issue number7
Publication statusPublished - Mar 2010


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