Phase III Trial in Metastatic Gastroesophageal Adenocarcinoma with Fluorouracil, Leucovorin Plus Either Oxaliplatin or Cisplatin: A Study of the Arbeitsgemeinschaft Internistische Onkologie

Salah‐Eddin Al‐Batran(Heidelberg University), J. T. Hartmann(Heidelberg University), Stephan Probst(Heidelberg University), Harald Schmalenberg(Heidelberg University), Stephan Hollerbach(Heidelberg University), Ralf‐Dieter Hofheinz(Heidelberg University), Volker Rethwisch(Heidelberg University), G. Seipelt(Heidelberg University), Nils Homann(Heidelberg University), G. Wilhelm(Heidelberg University), Gunter Schuch(Heidelberg University), Jan Stoehlmacher(Heidelberg University), Hans Günter Derigs(Heidelberg University), Susanna Hegewisch‐Becker(Heidelberg University), Johannes Grossmann(Heidelberg University), Claudia Pauligk(Heidelberg University), Akin Atmaca(Heidelberg University), Carsten Bokemeyer(Heidelberg University), Alexander Knuth(Heidelberg University), Elke Jäger(Heidelberg University)
Journal of Clinical Oncology
March 18, 2008
Cited by 784Open Access
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Abstract

PURPOSE: This study was designed to compare fluorouracil, leucovorin, and oxaliplatin with fluorouracil, leucovorin, and cisplatin in patients with advanced gastric cancer. PATIENTS AND METHODS: Patients with previously untreated advanced adenocarcinoma of the stomach or esophagogastric junction were randomly assigned to receive either fluorouracil 2,600 mg/m(2) via 24-hour infusion, leucovorin 200 mg/m(2), and oxaliplatin 85 mg/m(2) (FLO) every 2 weeks or fluorouracil 2,000 mg/m(2) via 24-hour infusion, leucovorin 200 mg/m(2) weekly, and cisplatin 50 mg/m(2) every 2 weeks (FLP). The primary end point was progression-free survival (PFS). RESULTS: Two hundred twenty patients (median age, 64 years; metastatic, 94%) were randomly assigned. FLO was associated with significantly less (any grade) anemia (54% v 72%), nausea (53% v 70%), vomiting (31% v 52%), alopecia (22% v 39%), fatigue (19% v 34%), renal toxicity (11% v 34%), thromboembolic events (0.9% v 7.8%), and serious adverse events related to the treatment (9% v 19%). FLP was associated with significantly less peripheral neuropathy (22% v 63%). There was a trend toward improved median PFS with FLO versus FLP (5.8 v 3.9 months, respectively; P = .077) and no significant difference in median overall survival (10.7 v 8.8 months, respectively). However, in patients older than 65 years (n = 94), treatment with FLO resulted in significantly superior response rates (41.3% v 16.7%; P = .012), time to treatment failure (5.4 v 2.3 months; P < .001), and PFS (6.0 v 3.1 month; P = .029) and an improved OS (13.9 v 7.2 months) as compared with FLP, respectively. CONCLUSION: FLO reduced toxicity as compared with FLP. In older adult patients, FLO also seemed to be associated with improved efficacy.


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