Efficacy and safety of lapatinib in Chinese breast cancer patients: a real-world study

BACKGROUND: Lapatinib is approved for the treatment of metastatic HER2-overexpressed breast cancer with capecitabine after progress on anthracycline, taxane, and trastuzumab in China. A post-marketing pharmacovigilance program was carried out to verify the real-world safety and the efficacy informat...

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Detalles Bibliográficos
Autores principales: Ye, Xuan, Luo, Xin, Du, Qiong, Li, Huan, Liu, Hong-Yue, Yu, Bo, Zhai, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154472/
https://www.ncbi.nlm.nih.gov/pubmed/32309387
http://dx.doi.org/10.21037/atm.2020.03.21
Descripción
Sumario:BACKGROUND: Lapatinib is approved for the treatment of metastatic HER2-overexpressed breast cancer with capecitabine after progress on anthracycline, taxane, and trastuzumab in China. A post-marketing pharmacovigilance program was carried out to verify the real-world safety and the efficacy information of lapatinib. METHODS: This was a prospective, non-interventional, long-term study in the real-world setting. All patients treated with lapatinib during the program (inclusion period 12 months) in Fudan University Shanghai Cancer Center (FUSCC) were included. The main outcome measures were progression-free survival (PFS) and incidence of adverse events. RESULTS: A total of 112 patients were enrolled. The median age was 52 years, 64.3% of patients were post-menopausal, 90 patients (80.4%) had stage IV disease, and the most common metastatic site was in the lung (43.8%), bone (30.4%), liver (26.8%), and brain (18.8%). About half of the patients (46.4%) experienced 3 or more systemic regimens before lapatinib. After a median follow-up of 34.3 months (range, 17.9–57.9 months), the median PFS was 8.1 months (95% CI, 5.8 to 10.4 months). Later phase of disease (stage IV), 3 or more prior treatments, pulmonary metastasis, liver metastasis, prior anthracycline or taxane, and poor adherence strongly correlated with worse survival (P<0.005). The grade 3 or 4 adverse events were diarrhea (9.8%), hand-foot syndrome (5.4%), and rash (4.5%). CONCLUSIONS: Upon implementation of lapatinib therapy in a real-world setting, the case mix was characterized by more early-stage breast cancer patients. The median PFS was slightly superior to what was published in the clinical trials. Pulmonary metastasis or liver metastasis significantly correlated with worse survival. We reported a similar prevalence of adverse events.