4.7 Article

Gemcitabine-oxaliplatin combination for ovarian cancer resistant to taxane-platinum treatment: a phase II study from the GINECO group

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BRITISH JOURNAL OF CANCER
卷 100, 期 4, 页码 601-607

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NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6604878

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combination chemotherapy; platinum-resistant; ovarian cancer; oxaliplatin; gemcitabine; toxicity

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Advanced ovarian carcinoma in early progression (<6 months) (AOCEP) is considered resistant to most cytotoxic drugs. Gemcitabine (GE) and oxaliplatin (OXA) have shown single-agent activity in relapsed ovarian cancer. Their combination was tested in patients with AOCEP in phase II study. Fifty patients pre-treated with platinum-taxane received q3w administration of OXA (100 mgm(-2), dl) and GE (1000 mgm(-2), d1, d8, 100-min infusion). Patient characteristics were a : median age 64 years (range 46-79), and 1 (84%) or 2 (16%) earlier lines of treatment. Haematological toxicity included grade 3-4 neutropaenia (33%), anaemia (8%), and thrombocytopaenia (19%). Febrile neutropaenia occurred in 3%. Non-haematological toxicity included grade 2-3 nausea or vomiting (34%), grade 3 fatigue (25%), and grade 2 alopecia (24%). Eighteen (37%) patients experienced response. Median progression-free (PF) and overall survivals (OS) were 4.6 and 11.4 months, respectively. The OXA-GE combination has high activity and acceptable toxicity in AOCEP patients. A comparison of the doublet OXA -GE with single-agent treatment is warranted.

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