Capecitabine and oxaliplatin for advanced esophagogastric cancer - PubMed (original) (raw)
Clinical Trial
. 2008 Jan 3;358(1):36-46.
doi: 10.1056/NEJMoa073149.
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- PMID: 18172173
- DOI: 10.1056/NEJMoa073149
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Clinical Trial
Capecitabine and oxaliplatin for advanced esophagogastric cancer
David Cunningham et al. N Engl J Med. 2008.
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Abstract
Background: We evaluated capecitabine (an oral fluoropyrimidine) and oxaliplatin (a platinum compound) as alternatives to infused fluorouracil and cisplatin, respectively, for untreated advanced esophagogastric cancer.
Methods: In a two-by-two design, we randomly assigned 1002 patients to receive triplet therapy with epirubicin and cisplatin plus either fluorouracil (ECF) or capecitabine (ECX) or triplet therapy with epirubicin and oxaliplatin plus either fluorouracil (EOF) or capecitabine (EOX). The primary end point was noninferiority in overall survival for the triplet therapies containing capecitabine as compared with fluorouracil and for those containing oxaliplatin as compared with cisplatin.
Results: For the capecitabine-fluorouracil comparison, the hazard ratio for death in the capecitabine group was 0.86 (95% confidence interval [CI], 0.80 to 0.99); for the oxaliplatin-cisplatin comparison, the hazard ratio for the oxaliplatin group was 0.92 (95% CI, 0.80 to 1.10). The upper limit of the confidence intervals for both hazard ratios excluded the predefined noninferiority margin of 1.23. Median survival times in the ECF, ECX, EOF, and EOX groups were 9.9 months, 9.9 months, 9.3 months, and 11.2 months, respectively; survival rates at 1 year were 37.7%, 40.8%, 40.4%, and 46.8%, respectively. In the secondary analysis, overall survival was longer with EOX than with ECF, with a hazard ratio for death of 0.80 in the EOX group (95% CI, 0.66 to 0.97; P=0.02). Progression-free survival and response rates did not differ significantly among the regimens. Toxic effects of capecitabine and fluorouracil were similar. As compared with cisplatin, oxaliplatin was associated with lower incidences of grade 3 or 4 neutropenia, alopecia, renal toxicity, and thromboembolism but with slightly higher incidences of grade 3 or 4 diarrhea and neuropathy.
Conclusions: Capecitabine and oxaliplatin are as effective as fluorouracil and cisplatin, respectively, in patients with previously untreated esophagogastric cancer. (Current Controlled Trials number, ISRCTN51678883 [controlled-trials.com].).
Copyright 2008 Massachusetts Medical Society.
Comment in
- Capecitabine and oxaliplatin for advanced esophagogastric cancer.
Bölke E, Peiper M, Budach W. Bölke E, et al. N Engl J Med. 2008 May 1;358(18):1965; author reply 1965. doi: 10.1056/NEJMc080178. N Engl J Med. 2008. PMID: 18450611 No abstract available. - Are capecitabine and oxaliplatin as effective as fluorouracil and cisplatin for gastroesophageal cancer?
Ajani JA. Ajani JA. Nat Clin Pract Gastroenterol Hepatol. 2008 Aug;5(8):414-5. doi: 10.1038/ncpgasthep1177. Epub 2008 Jun 17. Nat Clin Pract Gastroenterol Hepatol. 2008. PMID: 18560397 No abstract available. - Capecitabine and oxaliplatin for advanced esophagogastric cancer.
Cunningham D, Okines AF, Ashley S. Cunningham D, et al. N Engl J Med. 2010 Mar 4;362(9):858-9. doi: 10.1056/NEJMc0911925. N Engl J Med. 2010. PMID: 20200397 No abstract available.
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