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Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer

Anthracyclines and taxanes are very effective drugs in the treatment of advanced breast cancer. With G-CSF support, the dose-intensity of this combination can be increased by reducing the interval between chemotherapy cycles, the so-called ‘shortening of cycle time’. We treated 36 patients with adva...

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Autores principales: Lalisang, R I, Voest, E E, Wils, J A, Nortier, J W, Erdkamp, F L, Hillen, H F, Wals, J, Schouten, H C, Blijham, G H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363253/
https://www.ncbi.nlm.nih.gov/pubmed/10864197
http://dx.doi.org/10.1054/bjoc.2000.1202
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author Lalisang, R I
Voest, E E
Wils, J A
Nortier, J W
Erdkamp, F L
Hillen, H F
Wals, J
Schouten, H C
Blijham, G H
author_facet Lalisang, R I
Voest, E E
Wils, J A
Nortier, J W
Erdkamp, F L
Hillen, H F
Wals, J
Schouten, H C
Blijham, G H
author_sort Lalisang, R I
collection PubMed
description Anthracyclines and taxanes are very effective drugs in the treatment of advanced breast cancer. With G-CSF support, the dose-intensity of this combination can be increased by reducing the interval between chemotherapy cycles, the so-called ‘shortening of cycle time’. We treated 36 patients with advanced breast cancer in a multicentre phase I/II study. The treatment regimen consisted of epirubicin 75 mg m(−2)followed by paclitaxel 135 mg m(−2)(3 h) in combination with G-CSF. At least six patients were treated in each cohort and were evaluated over the first three cycles. Starting at an interval of 14 days, in subsequent cohorts of patients the interval could be shortened to 10 days. An 8-day interval was not feasible due mainly to incomplete neutrophil recovery at the day of the next scheduled cycle. In the 10-day interval cohort it was feasible to increase the paclitaxel dose to 175 mg m(−2). The haematological and non-haematological toxicity was relatively mild. No cumulative myelosuppression was observed over at least three consecutive cycles. In combination with G-CSF, epirubicin 75 mg m(−2)and paclitaxel 175 mg m(−2)could be safely administered every 10 days over at least three cycles, enabling a dose intensity of 52 and 122 mg m(−2)per week, respectively. © 2000 Cancer Research Campaign
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spelling pubmed-23632532009-09-10 Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer Lalisang, R I Voest, E E Wils, J A Nortier, J W Erdkamp, F L Hillen, H F Wals, J Schouten, H C Blijham, G H Br J Cancer Regular Article Anthracyclines and taxanes are very effective drugs in the treatment of advanced breast cancer. With G-CSF support, the dose-intensity of this combination can be increased by reducing the interval between chemotherapy cycles, the so-called ‘shortening of cycle time’. We treated 36 patients with advanced breast cancer in a multicentre phase I/II study. The treatment regimen consisted of epirubicin 75 mg m(−2)followed by paclitaxel 135 mg m(−2)(3 h) in combination with G-CSF. At least six patients were treated in each cohort and were evaluated over the first three cycles. Starting at an interval of 14 days, in subsequent cohorts of patients the interval could be shortened to 10 days. An 8-day interval was not feasible due mainly to incomplete neutrophil recovery at the day of the next scheduled cycle. In the 10-day interval cohort it was feasible to increase the paclitaxel dose to 175 mg m(−2). The haematological and non-haematological toxicity was relatively mild. No cumulative myelosuppression was observed over at least three consecutive cycles. In combination with G-CSF, epirubicin 75 mg m(−2)and paclitaxel 175 mg m(−2)could be safely administered every 10 days over at least three cycles, enabling a dose intensity of 52 and 122 mg m(−2)per week, respectively. © 2000 Cancer Research Campaign Nature Publishing Group 2000-06 2000-05-18 /pmc/articles/PMC2363253/ /pubmed/10864197 http://dx.doi.org/10.1054/bjoc.2000.1202 Text en Copyright © 2000 Cancer Research Campaign 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 Regular Article
Lalisang, R I
Voest, E E
Wils, J A
Nortier, J W
Erdkamp, F L
Hillen, H F
Wals, J
Schouten, H C
Blijham, G H
Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title_full Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title_fullStr Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title_full_unstemmed Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title_short Dose-dense epirubicin and paclitaxel with G-CSF: a study of decreasing intervals in metastatic breast cancer
title_sort dose-dense epirubicin and paclitaxel with g-csf: a study of decreasing intervals in metastatic breast cancer
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363253/
https://www.ncbi.nlm.nih.gov/pubmed/10864197
http://dx.doi.org/10.1054/bjoc.2000.1202
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