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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.
Afiliação
  • Ma X; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Li Y; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Li L; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Gao C; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Liu D; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Li H; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Zhao Z; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
  • Zhao B; Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Ann Med ; 54(1): 3085-3095, 2022 12.
Article em En | MEDLINE | ID: mdl-36331291
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 MESSAGESPresent 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias da Mama Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Ann Med Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Neoplasias da Mama Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Ann Med Assunto da revista: MEDICINA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
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