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Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment

Currently, there is no preferred standard chemotherapy regimen available for patients with metastatic triple negative breast cancer (mTNBC) and no cohort studies on the efficacy of vinorelbine plus platinum (NP) regimen in patients with mTNBC who failed to anthracyclines and/or taxanes have been rep...

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Autores principales: li, Meiying, Fan, Ying, Li, Qing, Zhang, Pin, Yuan, Peng, Ma, Fei, Wang, Jiayu, Luo, Yang, Cai, Ruigang, Chen, Shanshan, Li, Qiao, Xu, Binghe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985432/
https://www.ncbi.nlm.nih.gov/pubmed/26512619
http://dx.doi.org/10.1097/MD.0000000000001928
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author li, Meiying
Fan, Ying
Li, Qing
Zhang, Pin
Yuan, Peng
Ma, Fei
Wang, Jiayu
Luo, Yang
Cai, Ruigang
Chen, Shanshan
Li, Qiao
Xu, Binghe
author_facet li, Meiying
Fan, Ying
Li, Qing
Zhang, Pin
Yuan, Peng
Ma, Fei
Wang, Jiayu
Luo, Yang
Cai, Ruigang
Chen, Shanshan
Li, Qiao
Xu, Binghe
author_sort li, Meiying
collection PubMed
description Currently, there is no preferred standard chemotherapy regimen available for patients with metastatic triple negative breast cancer (mTNBC) and no cohort studies on the efficacy of vinorelbine plus platinum (NP) regimen in patients with mTNBC who failed to anthracyclines and/or taxanes have been reported. We present the single-center, retrospective experience of NP regimen in a total of 41 patients with mTNBC. All patients were treated with NP regimen, main combination used was vinorelbine-cisplatin in 34 patients (82.9%). The median follow-up was 36.8 months. Objective response rate was 34.1% (n = 14) in the whole study group. Three patients experienced complete response (7.3%), 11 patients acquired partial response (26.8%), stable disease was observed in 14 patients (34.1%), and 10 patients (24.4%) had progressive disease. Response evaluation was not applicable in 3 patients who received the treatment of NP regimen after surgical removal of the metastatic lesions. The median overall survival and progression-free survival were 18.9 months (95% confidence interval, 15.6–22.1 months) and 6.7 months (95% confidence interval, 2.9–10.5 months), respectively. The main adverse events were grade 3/4 neutropenia (n = 20, 48.8%) and grade 1/2 gastrointestinal toxicity (n = 20, 48.8%). NP regimen is active and tolerable in patients with mTNBC pretreated with anthracyclines and/or taxanes. Therefore, among other chemotherapy regimens, NP combination may provide a rational treatment option for this patient subset.
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spelling pubmed-49854322016-08-26 Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment li, Meiying Fan, Ying Li, Qing Zhang, Pin Yuan, Peng Ma, Fei Wang, Jiayu Luo, Yang Cai, Ruigang Chen, Shanshan Li, Qiao Xu, Binghe Medicine (Baltimore) 5700 Currently, there is no preferred standard chemotherapy regimen available for patients with metastatic triple negative breast cancer (mTNBC) and no cohort studies on the efficacy of vinorelbine plus platinum (NP) regimen in patients with mTNBC who failed to anthracyclines and/or taxanes have been reported. We present the single-center, retrospective experience of NP regimen in a total of 41 patients with mTNBC. All patients were treated with NP regimen, main combination used was vinorelbine-cisplatin in 34 patients (82.9%). The median follow-up was 36.8 months. Objective response rate was 34.1% (n = 14) in the whole study group. Three patients experienced complete response (7.3%), 11 patients acquired partial response (26.8%), stable disease was observed in 14 patients (34.1%), and 10 patients (24.4%) had progressive disease. Response evaluation was not applicable in 3 patients who received the treatment of NP regimen after surgical removal of the metastatic lesions. The median overall survival and progression-free survival were 18.9 months (95% confidence interval, 15.6–22.1 months) and 6.7 months (95% confidence interval, 2.9–10.5 months), respectively. The main adverse events were grade 3/4 neutropenia (n = 20, 48.8%) and grade 1/2 gastrointestinal toxicity (n = 20, 48.8%). NP regimen is active and tolerable in patients with mTNBC pretreated with anthracyclines and/or taxanes. Therefore, among other chemotherapy regimens, NP combination may provide a rational treatment option for this patient subset. Wolters Kluwer Health 2015-10-30 /pmc/articles/PMC4985432/ /pubmed/26512619 http://dx.doi.org/10.1097/MD.0000000000001928 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5700
li, Meiying
Fan, Ying
Li, Qing
Zhang, Pin
Yuan, Peng
Ma, Fei
Wang, Jiayu
Luo, Yang
Cai, Ruigang
Chen, Shanshan
Li, Qiao
Xu, Binghe
Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title_full Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title_fullStr Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title_full_unstemmed Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title_short Vinorelbine Plus Platinum in Patients with Metastatic Triple Negative Breast Cancer and Prior Anthracycline and Taxane Treatment
title_sort vinorelbine plus platinum in patients with metastatic triple negative breast cancer and prior anthracycline and taxane treatment
topic 5700
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985432/
https://www.ncbi.nlm.nih.gov/pubmed/26512619
http://dx.doi.org/10.1097/MD.0000000000001928
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