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Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer

INTRODUCTION: Weekly paclitaxel (Ptx) and q3w docetaxel (Dtx) are equivalent in adjuvant breast cancer treatment. Weekly Ptx is better tolerated than q3w Dtx and became the first choice in daily practice, even preoperatively. METHODS: To compare the efficacy and safety of the two regimens, a retrosp...

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Autores principales: Bacinschi, Xenia Elena, Anghel, Rodica Maricela, Toma, Paula Iuliana, Safta, Inga, Ilie, Alis, Ilie, Silvia Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051895/
https://www.ncbi.nlm.nih.gov/pubmed/32161494
http://dx.doi.org/10.2147/CMAR.S234527
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author Bacinschi, Xenia Elena
Anghel, Rodica Maricela
Toma, Paula Iuliana
Safta, Inga
Ilie, Alis
Ilie, Silvia Mihaela
author_facet Bacinschi, Xenia Elena
Anghel, Rodica Maricela
Toma, Paula Iuliana
Safta, Inga
Ilie, Alis
Ilie, Silvia Mihaela
author_sort Bacinschi, Xenia Elena
collection PubMed
description INTRODUCTION: Weekly paclitaxel (Ptx) and q3w docetaxel (Dtx) are equivalent in adjuvant breast cancer treatment. Weekly Ptx is better tolerated than q3w Dtx and became the first choice in daily practice, even preoperatively. METHODS: To compare the efficacy and safety of the two regimens, a retrospective analysis was performed in breast cancer patients (pts) referred for neoadjuvant, sequential, taxane-containing chemotherapy to the Institute of Oncology and Oncofort Clinic, Bucharest, between 2008 and 2017. RESULTS: Forty-seven cases were eligible, median age was 56 years (34–73 years), mainly stage IIIA–B (53.2%, 25 pts) and ductal invasive (70.2%, 33 pts) of which 24 pts (51%) received q3w Dtx and 23 pts (48.9%) weekly Ptx. The histological response rates were 62.5% (15 pts) and 73.7% (17 pts) (p=0.47), average dose-intensity was 87.7% and 96.7% (p=0.002) and grade III–IV toxicity rate was 12.5% and 13% (p=0.64), respectively. Pathologic response was correlated with immunophenotype, PgR expression, tumor size and backbone chemotherapy (p<0.05). DISCUSSION: Our study showed an improved efficacy of taxane’s weekly administration, probably due to a better tolerance and a lower rate of dose-impairing toxicities.
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spelling pubmed-70518952020-03-11 Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer Bacinschi, Xenia Elena Anghel, Rodica Maricela Toma, Paula Iuliana Safta, Inga Ilie, Alis Ilie, Silvia Mihaela Cancer Manag Res Original Research INTRODUCTION: Weekly paclitaxel (Ptx) and q3w docetaxel (Dtx) are equivalent in adjuvant breast cancer treatment. Weekly Ptx is better tolerated than q3w Dtx and became the first choice in daily practice, even preoperatively. METHODS: To compare the efficacy and safety of the two regimens, a retrospective analysis was performed in breast cancer patients (pts) referred for neoadjuvant, sequential, taxane-containing chemotherapy to the Institute of Oncology and Oncofort Clinic, Bucharest, between 2008 and 2017. RESULTS: Forty-seven cases were eligible, median age was 56 years (34–73 years), mainly stage IIIA–B (53.2%, 25 pts) and ductal invasive (70.2%, 33 pts) of which 24 pts (51%) received q3w Dtx and 23 pts (48.9%) weekly Ptx. The histological response rates were 62.5% (15 pts) and 73.7% (17 pts) (p=0.47), average dose-intensity was 87.7% and 96.7% (p=0.002) and grade III–IV toxicity rate was 12.5% and 13% (p=0.64), respectively. Pathologic response was correlated with immunophenotype, PgR expression, tumor size and backbone chemotherapy (p<0.05). DISCUSSION: Our study showed an improved efficacy of taxane’s weekly administration, probably due to a better tolerance and a lower rate of dose-impairing toxicities. Dove 2020-02-26 /pmc/articles/PMC7051895/ /pubmed/32161494 http://dx.doi.org/10.2147/CMAR.S234527 Text en © 2020 Bacinschi et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Bacinschi, Xenia Elena
Anghel, Rodica Maricela
Toma, Paula Iuliana
Safta, Inga
Ilie, Alis
Ilie, Silvia Mihaela
Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title_full Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title_fullStr Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title_full_unstemmed Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title_short Pathologic Response After Weekly Paclitaxel versus Docetaxel in Operable Breast Cancer
title_sort pathologic response after weekly paclitaxel versus docetaxel in operable breast cancer
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7051895/
https://www.ncbi.nlm.nih.gov/pubmed/32161494
http://dx.doi.org/10.2147/CMAR.S234527
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