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Efficacy comparisons of solvent-based paclitaxel, liposomal paclitaxel, nanoparticle albumin-bound paclitaxel, and docetaxel after neoadjuvant systemic treatment in breast cancer.

Authors :
Zhang, Weiwei
Wang, Ye
He, Jinzhi
Xu, Yinggang
Chen, Rui
Wan, Xinyu
Shi, Wenjie
Huang, Xiaofeng
Xu, Lu
Wang, Jue
Zha, Xiaoming
Source :
Nanomedicine: Nanotechnology, Biology & Medicine; Nov2023, Vol. 54, pN.PAG-N.PAG, 1p
Publication Year :
2023

Abstract

There are four kinds of taxanes: solvent-based paclitaxel (Sb-P), liposomal paclitaxel (Lps-P), nanoparticle albumin-bound paclitaxel (Nab-P), and docetaxel. This study aims to retrospectively evaluate the efficacy of different taxanes on neoadjuvant systemic treatment (NST) in breast cancer. Patients who were diagnosed with breast cancer and had received integral NST from August 2013 to April 2022 were enrolled. The efficacy was divided into total pathological complete response (total-pCR), breast pathological complete response (breast-pCR), and axillary pathological complete response (axillary-pCR) for in-depth analysis and discussion. The choice of taxane was an independent risk factor for total-pCR and breast-pCR rates. The highest total-pCR and breast-pCR rates were found in the Nab-P group. The difference was not significant among all the taxanes in the axillary-pCR rate. Nab-P significantly improved the total-pCR and breast-pCR rates. It should be the first choice among taxanes in NST for breast cancer. Compared to Sb-P, Lps-P, and docetaxel, Nab-P can significantly improve the total-pCR and breast-pCR rates. There was no difference in the axillary-pCR rates among four taxanes. Nab-P should be the first choice in the EC-T regimen with or without targeted therapy in NST for breast cancer. [Display omitted] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15499634
Volume :
54
Database :
Supplemental Index
Journal :
Nanomedicine: Nanotechnology, Biology & Medicine
Publication Type :
Academic Journal
Accession number :
173414151
Full Text :
https://doi.org/10.1016/j.nano.2023.102707