Efficacy and Side Effects in HER2-Positive Advanced Breast Cancer Patients Treated with Pyrrotinib: A Real-World Study in China

Xiaolei Wang, Chenxu Meng, Jing-jing Li, Yun Su, Fanfan Li, Jun Zhao
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Abstract

Background: Pyrotinib is a molecular and irreversible tyrosine kinase inhibitor independently developed in China, and its efficacy against HER2- positive breast cancer in the real world is not clear. In this study, we evaluated the efficacy and safety of pyrotinib in the treatment of HER2-positive advanced breast cancer based on real-world evidence. Materials and Methods: We designed a prospective observational study. Thirty-six patients with HER2-positive advanced breast cancer from a single medical center were included in the study from December 2018 to February 2021. All patients received the oral HER2 receptor inhibitor pyrotinib and received concurrent chemotherapy or endocrinotherapy. The follow-up endpoint is set as April 1, 2021. The primary endpoint is Objective Response Rate (ORR) and Disease Control Rate (DCR), and the secondary endpoint is Progression- Free Survival (PFS) and related side effects. Results: By the end point of follow-up, a total of 17 patients had progressed (including 6 deaths), and the progression-free survival rate was 52.78%. The median PFS was 13months (PFS range: 3-22 months). As the best response, 4 patients achieved CR, 20 patients achieved PR, 9 patients achieved SD, and 3 patient developed PD. The ORR was 66.67% and DCR was 91.67%. In the analysis, first-line pyrotinib treatment appeared to have higher ORR (88.88% vs 59.26%), but there was no significant difference. In addition, pyrotinib showed significant efficacy in patients with brain metastases, with an ORR of 42.85%. In terms of safety, the incidence of diarrhea was 80.55%, but only 4 patients had grade 3 diarrhea, which was tolerable after the drug dose was reduced; 1 patient had grade 4 neutropenia and grade 3 and thrombocytopenia, which were considered to be related to the chemotherapy drugs. The incidence of other adverse reactions was low, and all were grade 1 to 2. Conclusion: Pyrotinib combined with chemotherapy has a significant effect on HER2-positive breast cancer, and there is still a high ORR in patients who fail multiple lines of treatment. Side effects are overall controllable and safe.
吡罗替尼治疗HER2阳性晚期癌症患者的疗效和副作用:中国的一项现实世界研究
背景:派洛替尼是我国自主研发的一种分子不可逆酪氨酸激酶抑制剂,其在现实世界中对HER2阳性乳腺癌症的疗效尚不清楚。在这项研究中,我们根据现实世界的证据评估了焦替尼治疗HER2阳性晚期癌症的疗效和安全性。材料和方法:我们设计了一项前瞻性的观察性研究。2018年12月至2021年2月,来自一家医疗中心的36名HER2阳性晚期癌症患者被纳入研究。所有患者均接受口服HER2受体抑制剂吡替尼,并同时接受化疗或内分泌治疗。随访终点设定为2021年4月1日。主要终点是客观反应率(ORR)和疾病控制率(DCR),次要终点是无进展生存率(PFS)和相关副作用。结果:到随访结束时,共有17名患者取得了进展(包括6例死亡),无进展生存率为52.78%。中位PFS为13个月(PFS范围:3-22个月)。作为最佳反应,4名患者获得CR,20名患者获得PR,9名患者获得SD,3名患者出现PD。ORR为66.67%,DCR为91.67%。在分析中,一线吡替尼治疗似乎具有更高的ORR(88.88%与59.26%),但没有显著差异。此外,吡替尼在脑转移患者中显示出显著疗效,ORR为42.85%,安全性方面,腹泻发生率为80.55%,但只有4名患者出现3级腹泻,药物剂量降低后可耐受;1名患者有4级中性粒细胞减少症和3级血小板减少症,这被认为与化疗药物有关。其他不良反应发生率较低,均为1~2级。结论:派洛替尼联合化疗治疗HER2阳性乳腺癌症疗效显著,但多途径治疗失败的患者仍有较高的ORR。副作用总体可控且安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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