Breast Cancer, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
Ann Med. 2022 Dec;54(1):3085-3095. doi: 10.1080/07853890.2022.2139411.
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 combining pyrotinib to treat brain metastasis in patients with HER2-positive advanced BC based upon clinical data.
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.
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%) ( ≤ .05).
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.
广泛应用抗 HER2 靶向治疗显著改善了 HER2 阳性晚期乳腺癌(BC)的预后,但仍难以治疗脑转移。本研究基于临床资料,探讨了联合吡咯替尼治疗 HER2 阳性晚期 BC 伴脑转移(BM)患者的有效方法。
本研究纳入 61 例 HER2 阳性 BC 伴 BM 患者,采用吡咯替尼为基础的方案治疗。全身方案包括吡咯替尼联合卡培他滨、吡咯替尼联合白蛋白紫杉醇、吡咯替尼联合长春瑞滨。分析各联合方案的无进展生存期(PFS)、总生存期(OS)、临床获益率(CBR)和客观缓解率(ORR),以及药物相关不良事件(AE)。
BM 患者接受吡咯替尼为基础的全身治疗后中位 PFS(mPFS)和中位 OS(mOS)分别为 8.6 个月和 18.0 个月。不同方案中,吡咯替尼联合白蛋白紫杉醇方案在 PFS 和 OS 方面优于吡咯替尼联合卡培他滨和吡咯替尼联合长春瑞滨方案。3 种方案中枢神经系统(CNS)ORR 无显著差异,但白蛋白紫杉醇联合方案外周 ORR 最佳(84.6%)( ≤ .05)。
吡咯替尼为基础的联合治疗方案安全,用于治疗 HER2 阳性脑转移。与长春瑞滨或卡培他滨相比,吡咯替尼联合白蛋白紫杉醇更有效且毒性更小,是治疗 HER2 阳性脑转移的首选方案。
本研究探讨了联合吡咯替尼治疗 HER2 阳性晚期脑转移的有效方法。结果证实,吡咯替尼为基础的联合治疗方案安全有效,可治疗 HER2 阳性脑转移。因此,尽管吡咯替尼对转移瘤的治疗有效,但应用抗 HER2 靶向治疗治疗脑转移仍然有效。