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A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer

The docetaxel–carboplatin combination is active and well tolerated in patients with epithelial ovarian cancer. We added epirubicin to this combination to investigate additional benefits of anthracyclines in epithelial ovarian cancer. Twenty-one patients, FIGO Ic-IV, performance status 0–1, were trea...

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Autores principales: O'Neill, V J, Kaye, S B, Reed, N S, Paul, J, Davis, J A, Vasey, P A
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375366/
https://www.ncbi.nlm.nih.gov/pubmed/11986768
http://dx.doi.org/10.1038/sj.bjc.6600259
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author O'Neill, V J
Kaye, S B
Reed, N S
Paul, J
Davis, J A
Vasey, P A
author_facet O'Neill, V J
Kaye, S B
Reed, N S
Paul, J
Davis, J A
Vasey, P A
author_sort O'Neill, V J
collection PubMed
description The docetaxel–carboplatin combination is active and well tolerated in patients with epithelial ovarian cancer. We added epirubicin to this combination to investigate additional benefits of anthracyclines in epithelial ovarian cancer. Twenty-one patients, FIGO Ic-IV, performance status 0–1, were treated in four dose cohorts. Docetaxel was fixed at 75 mg m(−2), carboplatin doses were AUC 4–5 and epirubicin doses were 50–60 mg m(−2). Drugs were given on day 1, every 3 weeks, except in cohort 3, where epirubicin was given on day 8. Dexamethasone was given prophylactically. One dose-limiting toxicity occurred in cohorts 1, 2 and 4, two occurred in cohort 3. Complicated neutropenia occurred in two patients in cohorts 1 and 2 and one patient in cohorts 3 and 4. Two patients experienced grade III diarrhoea or stomatitis in cohort 1 and two in cohort 3. There were no treatment-related deaths. Grade II sensory neuropathy occurred in one patient. No cardiac toxicity or significant oedema was observed. The overall response rate was 36%, and 62% were CA125 responders. The predefined maximum tolerated dose was exceeded in cohort 3. The cohort 4 dose level (epirubicin 50 mg m(−2), carboplatin AUC 4, docetaxel 75 mg m(−2)), warrants further study. British Journal of Cancer (2002) 86, 1385–1390. DOI: 10.1038/sj/bjc/6600259 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23753662009-09-10 A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer O'Neill, V J Kaye, S B Reed, N S Paul, J Davis, J A Vasey, P A Br J Cancer Clinical The docetaxel–carboplatin combination is active and well tolerated in patients with epithelial ovarian cancer. We added epirubicin to this combination to investigate additional benefits of anthracyclines in epithelial ovarian cancer. Twenty-one patients, FIGO Ic-IV, performance status 0–1, were treated in four dose cohorts. Docetaxel was fixed at 75 mg m(−2), carboplatin doses were AUC 4–5 and epirubicin doses were 50–60 mg m(−2). Drugs were given on day 1, every 3 weeks, except in cohort 3, where epirubicin was given on day 8. Dexamethasone was given prophylactically. One dose-limiting toxicity occurred in cohorts 1, 2 and 4, two occurred in cohort 3. Complicated neutropenia occurred in two patients in cohorts 1 and 2 and one patient in cohorts 3 and 4. Two patients experienced grade III diarrhoea or stomatitis in cohort 1 and two in cohort 3. There were no treatment-related deaths. Grade II sensory neuropathy occurred in one patient. No cardiac toxicity or significant oedema was observed. The overall response rate was 36%, and 62% were CA125 responders. The predefined maximum tolerated dose was exceeded in cohort 3. The cohort 4 dose level (epirubicin 50 mg m(−2), carboplatin AUC 4, docetaxel 75 mg m(−2)), warrants further study. British Journal of Cancer (2002) 86, 1385–1390. DOI: 10.1038/sj/bjc/6600259 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-05-06 /pmc/articles/PMC2375366/ /pubmed/11986768 http://dx.doi.org/10.1038/sj.bjc.6600259 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Clinical
O'Neill, V J
Kaye, S B
Reed, N S
Paul, J
Davis, J A
Vasey, P A
A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title_full A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title_fullStr A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title_full_unstemmed A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title_short A dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
title_sort dose-finding study of carboplatin–epirubicin–docetaxel in advanced epithelial ovarian cancer
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375366/
https://www.ncbi.nlm.nih.gov/pubmed/11986768
http://dx.doi.org/10.1038/sj.bjc.6600259
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