Liang Xu, Gui Xinyu, Yan Ying, Di Lijun, Liu Xiaoran, Li Huiping, Song Guohong
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Breast Oncology, Peking University Cancer Hospital and Institute, Beijing, People's Republic of China.
Oncologist. 2024 Feb 2;29(2):e198-e205. doi: 10.1093/oncolo/oyad228.
Pyrotinib is currently approved for the treatment of HER2-positive advanced breast cancer in China. Data on the overall survival (OS) and efficacy in patients with brain metastasis (BM) remain scarce. This study evaluated the effectiveness of pyrotinib in a real-world setting, especially in patients with BM.
We reviewed patients with metastatic breast cancer treated with pyrotinib-based therapy between June 2018 and June 2022. Progression-free survival (PFS), OS, objective response rate, and safety were analyzed following the administration of pyrotinib.
A total of 239 patients were included. The median PFS in patients who received pyrotinib-based therapy as first-line (15/239), second-line (115/239), or third-or-higher-line (109/239) treatment was 14.00, 9.33, and 8.20 months, respectively, and the median OS was not reached, 29.07 and 22.23 months, respectively. The median PFS in patients who pretreated with trastuzumab (214/239), trastuzumab plus pertuzumab (22/239), lapatinib (68/239), or trastuzumab emtansine (14/239) was 9.33, 6.87, 7.20, and 7.20 months, respectively. In 61 patients with BM, the median PFS was 7.50 months, the median central nervous system (CNS)-PFS was 11.17 months, and the median OS was 21.27 months. Furthermore, 19 patients with concomitant brain radiotherapy tended to achieve a longer OS than 42 patients without radiation (34.17 vs. 20.70 months, P = .112).
Long-term outcomes of pyrotinib-based therapy are promising for patients with HER2-positive metastatic breast cancer in real world and in patients with BM, regardless of the treatment lines and prior anti-HER2 therapies.
吡咯替尼目前在中国被批准用于治疗HER2阳性晚期乳腺癌。关于脑转移(BM)患者的总生存期(OS)和疗效的数据仍然很少。本研究评估了吡咯替尼在真实世界中的有效性,尤其是在BM患者中的有效性。
我们回顾了2018年6月至2022年6月期间接受以吡咯替尼为基础治疗的转移性乳腺癌患者。在给予吡咯替尼后分析无进展生存期(PFS)、OS、客观缓解率和安全性。
共纳入239例患者。接受以吡咯替尼为基础治疗作为一线(15/239)、二线(115/239)或三线及以上(109/239)治疗的患者的中位PFS分别为14.00、9.33和8.20个月,中位OS未达到、为29.07和22.23个月。接受曲妥珠单抗(214/239)、曲妥珠单抗加帕妥珠单抗(22/239)、拉帕替尼(68/239)或曲妥珠单抗恩美曲妥珠单抗(14/239)预处理的患者的中位PFS分别为9.33、6.87、7.20和7.20个月。在61例BM患者中,中位PFS为7.50个月,中位中枢神经系统(CNS)-PFS为11.17个月,中位OS为21.27个月。此外,19例接受同步脑放疗的患者的OS往往比42例未接受放疗的患者更长(34.17对20.70个月,P = 0.112)。
对于HER2阳性转移性乳腺癌患者以及BM患者,无论治疗线数和既往抗HER2治疗如何,以吡咯替尼为基础的治疗的长期结果都是有希望的。