Literature DB >> 16702612

Capecitabine, epirubicin and cisplatin in the treatment of oesophagogastric adenocarcinoma.

S Corporaal1, W M Smit, M G V M Russel, J van der Palen, H Boot, M C J C Legdeur.   

Abstract

BACKGROUND: Inoperable or metastatic oesophagogastric adenocarcinoma has a poor prognosis. From the many different chemotherapeutic regimens used in the past, a combination of epirubicin, cisplatin and continuous 5-fluorouracil infusion (ECF) showed a consistent response rate of +/- 50% with acceptable toxicity. Continuous 5-FU infusion may be replaced by oral fluoropyrimidines. Here we evaluate treatment with epirubicin and cisplatin combined with oral capecitabine (ECC), replacing intravenous 5-FU infusion.
METHODS: Retrospectively, we analysed 23 consecutive patients who were treated with epirubicin, cisplatin and oral capecitabine for inoperable or metastatic oesophagogastric adenocarcinoma during 2002 and 2003.
RESULTS: The overall response rate was 57%; another 26% achieved stable disease and only 17% had progressive disease. The median duration of response was 6.4 months; the median survival was 9.0 months. Previously treated patients (n=10) had a significantly worse overall response rate (20%) compared with previously untreated patients (85%). A nonsignificant difference in median survival was found between these groups (3.9 vs 9.8 months in previously treated vs untreated patients). An acceptable incidence of grade 3 and 4 toxicity was found.
CONCLUSION: Capecitabine in combination with epirubicin and cisplatin is an effective and safe alternative to ECF, without the risks of a continuous venous access.

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Year:  2006        PMID: 16702612

Source DB:  PubMed          Journal:  Neth J Med        ISSN: 0300-2977            Impact factor:   1.422


  2 in total

1.  Capecitabine treatment patterns in patients with gastroesophageal cancer in the United States.

Authors:  Muhammad Wasif Saif; Nianwen Shi; Susan Zelt
Journal:  World J Gastroenterol       Date:  2009-09-21       Impact factor: 5.742

2.  High-level copy number gains of established and potential drug target genes in gastric cancer as a lead for treatment development and selection.

Authors:  Mariette Labots; Tineke E Buffart; Josien C Haan; Nicole C T van Grieken; Marianne Tijssen; Cornelis J H van de Velde; Heike I Grabsch; Bauke Ylstra; Beatriz Carvalho; Remond J A Fijneman; Henk M W Verheul; Gerrit A Meijer
Journal:  Cell Oncol (Dordr)       Date:  2013-12-31       Impact factor: 6.730

  2 in total

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