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Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases

OBJECTIVES: Extensive application of anti-HER2 targeted therapy improves significantly the HER2-positive advanced breast cancer (BC) prognosis, however, it is still difficult to treat brain metastasis. In current study, we explored effective approaches via combining pyrotinib to treat brain metastas...

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Autores principales: Ma, Xiaoping, Li, Yan, Li, Li, Gao, Chunyan, Liu, Dan, Li, Hongyu, Zhao, Zhenhui, Zhao, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639475/
https://www.ncbi.nlm.nih.gov/pubmed/36331291
http://dx.doi.org/10.1080/07853890.2022.2139411
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author Ma, Xiaoping
Li, Yan
Li, Li
Gao, Chunyan
Liu, Dan
Li, Hongyu
Zhao, Zhenhui
Zhao, Bing
author_facet Ma, Xiaoping
Li, Yan
Li, Li
Gao, Chunyan
Liu, Dan
Li, Hongyu
Zhao, Zhenhui
Zhao, Bing
author_sort Ma, Xiaoping
collection PubMed
description OBJECTIVES: Extensive application of anti-HER2 targeted therapy improves significantly the HER2-positive advanced breast cancer (BC) prognosis, however, it is still difficult to treat brain metastasis. In current study, we explored effective approaches via combining pyrotinib to treat brain metastasis in patients with HER2-positive advanced BC based upon clinical data. MATERIALS AND METHODS: Current study included 61 HER2-positive BC patients with brain metastases (BM) who were treated by pyrotinib-based regimens. The systemic regimens included pyrotinib combined with capecitabine, pyrotinib combined with nab-paclitaxel, and pyrotinib combined with vinorelbine. Patients’ progression-free survival (PFS), overall survival (OS), clinical benefit rate (CBR) and objective response rate (ORR), as well as drug-related adverse events (AEs) in regard of each combination regimen were analyzed. RESULTS: Pyrotinib-based systemic therapy resulted in 8.6 months median PFS (mPFS) and 18.0 months median OS (mOS) among the BM patients. Regarding different regimens, the combination of pyrotinib with nab-paclitaxel was superior to the combination with capecitabine and vinorelbine with respect to PFS and OS. The central nervous system (CNS) ORR did not showcase significant difference among 3 regimens, however, nab-paclitaxel combined regimen obtained the best peripheral ORR (84.6%) (p ≤ .05). CONCLUSIONS: Pyrotinib-based combination therapy is safe for HER2-positive brain metastasis treatment. Compared with vinorelbine or capecitabine, pyrotinib combined with nab-paclitaxel is more effective with less toxicity, which is the preferable regimen for HER2-positive brain metastasis. KEY MESSAGES: Present investigation investigated effective methods through combining pyrotinib to treat brain metastasis with HER2-positive advanced brain cancer. The outcomes verified that pyrotinib-based combination therapy was safe and efficient to treat HER2-positive brain metastasis. Therefore, it is effective to treat brain metastasis applying anti-HER2 targeted therapies although pyrotinib showcases efficiency regarding its treatments for the metastasis.
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spelling pubmed-96394752022-11-08 Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases Ma, Xiaoping Li, Yan Li, Li Gao, Chunyan Liu, Dan Li, Hongyu Zhao, Zhenhui Zhao, Bing Ann Med Oncology OBJECTIVES: Extensive application of anti-HER2 targeted therapy improves significantly the HER2-positive advanced breast cancer (BC) prognosis, however, it is still difficult to treat brain metastasis. In current study, we explored effective approaches via combining pyrotinib to treat brain metastasis in patients with HER2-positive advanced BC based upon clinical data. MATERIALS AND METHODS: Current study included 61 HER2-positive BC patients with brain metastases (BM) who were treated by pyrotinib-based regimens. The systemic regimens included pyrotinib combined with capecitabine, pyrotinib combined with nab-paclitaxel, and pyrotinib combined with vinorelbine. Patients’ progression-free survival (PFS), overall survival (OS), clinical benefit rate (CBR) and objective response rate (ORR), as well as drug-related adverse events (AEs) in regard of each combination regimen were analyzed. RESULTS: Pyrotinib-based systemic therapy resulted in 8.6 months median PFS (mPFS) and 18.0 months median OS (mOS) among the BM patients. Regarding different regimens, the combination of pyrotinib with nab-paclitaxel was superior to the combination with capecitabine and vinorelbine with respect to PFS and OS. The central nervous system (CNS) ORR did not showcase significant difference among 3 regimens, however, nab-paclitaxel combined regimen obtained the best peripheral ORR (84.6%) (p ≤ .05). CONCLUSIONS: Pyrotinib-based combination therapy is safe for HER2-positive brain metastasis treatment. Compared with vinorelbine or capecitabine, pyrotinib combined with nab-paclitaxel is more effective with less toxicity, which is the preferable regimen for HER2-positive brain metastasis. KEY MESSAGES: Present investigation investigated effective methods through combining pyrotinib to treat brain metastasis with HER2-positive advanced brain cancer. The outcomes verified that pyrotinib-based combination therapy was safe and efficient to treat HER2-positive brain metastasis. Therefore, it is effective to treat brain metastasis applying anti-HER2 targeted therapies although pyrotinib showcases efficiency regarding its treatments for the metastasis. Taylor & Francis 2022-11-04 /pmc/articles/PMC9639475/ /pubmed/36331291 http://dx.doi.org/10.1080/07853890.2022.2139411 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oncology
Ma, Xiaoping
Li, Yan
Li, Li
Gao, Chunyan
Liu, Dan
Li, Hongyu
Zhao, Zhenhui
Zhao, Bing
Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title_full Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title_fullStr Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title_full_unstemmed Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title_short Pyrotinib-based treatments in HER2-positive breast cancer patients with brain metastases
title_sort pyrotinib-based treatments in her2-positive breast cancer patients with brain metastases
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9639475/
https://www.ncbi.nlm.nih.gov/pubmed/36331291
http://dx.doi.org/10.1080/07853890.2022.2139411
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