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Capecitabine and oxaliplatin for advanced esophagogastric cancer

Capecitabine and oxaliplatin for advanced esophagogastric cancer
Capecitabine and oxaliplatin for advanced esophagogastric cancer
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
36-46
Cunningham, David
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Starling, Naureen
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Rao, Sheela
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Iveson, Timothy
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Nicolson, Marianne
ed578571-b31b-4046-a15e-ce4c56f424e1
Coxon, Fareeda
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Middleton, Gary
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Daniel, Francis
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Oates, Jacqueline
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Norman, Andrew Richard
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Cunningham, David
c40c8fe4-7eac-4b98-aaa5-b866da1e32ab
Starling, Naureen
5ea2ce97-d3f9-465f-a91a-79798a0c9b74
Rao, Sheela
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Iveson, Timothy
867cb6c5-ea9a-4521-a4cc-4cd4d2503b3a
Nicolson, Marianne
ed578571-b31b-4046-a15e-ce4c56f424e1
Coxon, Fareeda
861b2bac-87a1-4b70-95c1-6a28c5035c8c
Middleton, Gary
31c645ca-3e55-491c-866e-370b6bbd91e5
Daniel, Francis
74cadea0-11db-4cfd-b809-3097e7950f0e
Oates, Jacqueline
95e92193-7150-4f4d-93fd-57918eebacbd
Norman, Andrew Richard
888997c3-54f9-490f-9ee3-2d23753c4c7e

Cunningham, David, Starling, Naureen, Rao, Sheela, Iveson, Timothy, Nicolson, Marianne, Coxon, Fareeda, Middleton, Gary, Daniel, Francis, Oates, Jacqueline and Norman, Andrew Richard (2008) Capecitabine and oxaliplatin for advanced esophagogastric cancer. New England Journal of Medicine, 358 (1), 36-46.

Record type: Article

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

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Published date: 3 January 2008

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Local EPrints ID: 79353
URI: http://eprints.soton.ac.uk/id/eprint/79353
PURE UUID: 3c2757f4-d870-41bf-a952-75b749b0eaa3
ORCID for Timothy Iveson: ORCID iD orcid.org/0000-0002-4681-2712

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Date deposited: 15 Mar 2010
Last modified: 23 Jul 2022 01:42

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Contributors

Author: David Cunningham
Author: Naureen Starling
Author: Sheela Rao
Author: Timothy Iveson ORCID iD
Author: Marianne Nicolson
Author: Fareeda Coxon
Author: Gary Middleton
Author: Francis Daniel
Author: Jacqueline Oates
Author: Andrew Richard Norman

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