Docetaxel combined with irinotecan or 5-fluorouracil in patients with advanced oesophago-gastric cancer: a randomised phase II study

作者：Roy A; Cunningham D^*; Hawkins R; Sorbye H; Adenis A; Barcelo J R; Lopez Vivanco G; Adler G; Canon J L; Lofts F; Castanon C; Fonseca E; Rixe O; Aparicio J; Cassinello J; Nicolson M; Mousseau M; Schalhorn A; D' Hondt L; Kerger J; Hossfeld D K; Giron C Garcia; Rodriguez R; Schoffski P; Misset J L

来源：British Journal of Cancer, 2012, 107(3): 435-441.

DOI：10.1038/bjc.2012.286

• oesophago-gastric cancer
• docetaxel
• irinotecan
• 5-fluorouracil

BACKGROUND: Docetaxel and irinotecan chemotherapy have shown good efficacy in the treatment of advanced oesophago-gastric cancer. This randomised phase II study evaluated the efficacy and toxicity profile of two non-platinum docetaxel-based doublet regimens in advanced oesophago-gastric cancer. %26lt;br%26gt;METHODS: Chemotherapy-naive patients with advanced oesophago-gastric cancer were randomised to receive either 3-weekly DI (docetaxel 60 mg m(-2) plus irinotecan 250 mg m(-2) (Day 1)) or 3-weekly DF (docetaxel 85 mg m(-2) (Day 1) followed by 5-fluorouracil 750 mg m(-2) per day as a continuous infusion (Days 1-5)). %26lt;br%26gt;RESULTS: A total of 85 patients received DI (n = 42) or DF (n = 43). The primary endpoint was overall response rate (ORR). The ORR and time to progression (TTP) in the evaluable population (n = 65) were 37.5% (DI) vs 33.3% (DF), and 4.2 months vs 4.4 months, respectively. In the intent-to-treat population, the observed ORR, TTP and median overall survival were similar between the two groups. Grade 3-4 neutropenia, febrile neutropenia and diarrhoea were more frequent in the DI arm as compared with the DF arm (83.3% vs 69.8%, 40.5% vs 18.6%, and 42.9% vs 16.3%, respectively). %26lt;br%26gt;CONCLUSION: Both docetaxel-based doublet regimens show comparable efficacy; however, the DF regimen was associated with a better toxicity profile and is an alternative treatment option for patients in whom platinum-based regimens are unsuitable. British Journal of Cancer (2012) 107, 435-441. doi: 10.1038/bjc.2012.286 www.bjcancer.

• 出版日期2012-7-24