Biweekly fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) for patients with metastatic adenocarcinoma of the stomach or esophagogastric junction: a phase II trial of the Arbeitsgemeinschaft Internistische Onkologie

被引:202
作者
Al-Batran, S. -E. [1 ]
Hartmann, J. T. [2 ]
Hofheinz, R. [3 ]
Homann, N. [4 ]
Rethwisch, V. [5 ]
Probst, S. [6 ]
Stoehlmacher, J. [7 ]
Clemens, M. R. [8 ]
Mahlberg, R. [8 ]
Fritz, M. [9 ]
Seipelt, G. [10 ]
Sievert, M. [11 ]
Pauligk, C. [1 ]
Atmaca, A. [1 ]
Jaeger, E. [1 ]
机构
[1] Krankenhaus NW Frankfurt, Klin Onkol & Hamatol, D-60488 Frankfurt, Germany
[2] Univ Tubingen, SW Canc Ctr, Dept Med Oncol Hematol Immunol Rheumatol & Pulmol, D-72074 Tubingen, Germany
[3] Univ Klinikum Mannheim, Dept Med 3, Mannheim, Germany
[4] Med Univ Lubeck, Dept Med 1, Lubeck, Germany
[5] Katholisches Krankenhaus, Dept Hematol & Oncol, Hagen, Germany
[6] Stadt Kliniken, Dept Hematol & Oncol, Bielefeld, Germany
[7] Univ Klinikum Carl Gustav, Dept Internal Med 1, Dresden, Germany
[8] Dept Med 1, Trier, Germany
[9] Krankenhaus Bad Cannstatt, Stuttgart, Germany
[10] Gemeinsch Praxis Hamatol & Internist Onkol, Bad Soden, Germany
[11] Sanofi Aventis Deutschland GmbH, Med Oncol, Berlin, Germany
关键词
docetaxel; esophageal; FLOT; gastric; oxaliplatin;
D O I
10.1093/annonc/mdn403
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The combination of docetaxel (Taxotere), cisplatin, and fluorouracil improved efficacy in gastric cancer, but was associated with substantial toxicity. This study was designed to incorporate docetaxel into a tolerable biweekly (once every 2 weeks) oxaliplatin-based chemotherapy regimen. Patients and methods: Patients with measurable, metastatic adenocarcinoma of the stomach or esophagogastric junction and no prior chemotherapy received oxaliplatin 85 mg/m(2), leucovorin 200 mg/m(2), and fluorouracil 2600 mg/m(2) as a 24-h infusion in combination with docetaxel 50 mg/m(2) (FLOT) on day 1 every 2 weeks. Prophylactic growth factors were not administered. Results: Fifty-nine patients were enrolled; 54 received treatment. Patients had a median age of 60 years (range 29-76) and most (93%) of them had metastatic disease. Objective responses were observed in 57.7% of patients with a median time to treatment response of 1.54 months. Median progression-free survival (PFS) and overall survival were 5.2 and 11.1 months, respectively. Twenty-five percent of patients experienced prolonged (> 12 months) PFS. Frequent (> 10%) grade 3 or 4 toxic effects included neutropenia in 26 (48.1%), leukopenia in 15 (27.8%), diarrhea in 8 (14.8%), and fatigue in 6 (11.1%) patients. Complicated neutropenia was observed in two (3.8%) patients, only. Conclusions: Biweekly FLOT is active and has a favorable safety profile.
引用
收藏
页码:1882 / 1887
页数:6
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