British Journal of Cancer · 2002 · 16 citations · 11 references
MedicineOncologyPharmacotherapyCancer PharmacologyChemotherapyGastrointestinal OncologyCombination Cancer TherapyEsophageal CancerGastrointestinal Cancer PharmacotherapyMalignant NeoplasmsPancreatic CancerToxicity ManagementComplete Response AssessmentEsophageal Cancer PharmacotherapyIrinotecan-based TherapyPancreatic Cancer Pharmacotherapy
Irinotecan, mitomycin and cisplatin all demonstrate activity in gastro-oesophageal cancers. This novel combination was administered to outpatients with previously untreated inoperable gastro-oesophageal or pancreatic cancer, in a 28-day cycle. A total of 26 out of 31 patients with gastro-oesophageal cancer and 12 out of 14 patients with pancreatic cancer have been treated with this combination, and were evaluable for response. The overall response rates for patients with gastro-oesophageal cancer was 42%, with a median survival of 9.5 months. In patients with pancreatic cancer, the overall response rate was 42% with a median survival of 8 months. There was a statistically significant increase in survival between those patients who achieved a stable disease response and those who achieved either a partial response or complete response. The toxicity profiles for both cancers were virtually identical. There were five treatment-related deaths, and a high admission rate (42%). Thus irinotecan, mitomycin and cisplatin is a new combination with activity in inoperable upper gastro-oesophageal cancers, but with a high toxicity profile. Future developments include reducing the dose of irinotecan and number of cycles of therapy to four.
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Howard A. Burris, Malcolm J. Moore, John Sahl Andersen et al. · Journal of Clinical Oncology · 1997 · 5.9K citations
Medicine, Oncology, Pharmacotherapy +16
U. Vanhoefer, Philippe Rougier, H. Wilke et al. · Journal of Clinical Oncology · 2000 · 533 citations
Medicine, Oncology, Pharmacology +16