Qu Yanchun, Liu Yufeng, Ding Kailin, Li Yong, Hong Xiaoyu, Zhang Haibo
Department of Oncology, The Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, People's Republic of China.
Department of Oncology, Guangdong Provincial Hospital of Traditional Chinese Medicine, Guangzhou, People's Republic of China.
Onco Targets Ther. 2021 Mar 2;14:1581-1588. doi: 10.2147/OTT.S289876. eCollection 2021.
Human epidermal growth factor receptor2 () overexpression/amplification is associated with high malignancy, rapid disease progression and poor overall survival in breast cancer. The application of anti- drugs has greatly improved the survival of patients with -positive breast cancer, but drug resistance issues affect the long-term efficacy. The mutation is considered to be one of the reasons for resistance to anti- therapy, and there is currently no standard treatment. We report for the first time the detection of amplification with mutation by second-generation sequencing (NGS) in a 57-year-old hormone receptor-negative, -positive woman with advanced breast cancer who was resistant to multi-line anti- therapies. She subsequently received pyrotinib combined with capecitabine treatment and achieved partial response. The small-molecule pan- family irreversible inhibitor pyrotinib combined with capecitabine has shown a promising effect in the treatment of mutation-induced resistance, but the molecular mechanism and efficacy need to be further verified.
人表皮生长因子受体2()过表达/扩增与乳腺癌的高恶性、疾病快速进展及总体生存率低相关。抗药物的应用极大地提高了阳性乳腺癌患者的生存率,但耐药问题影响长期疗效。突变被认为是抗治疗耐药的原因之一,目前尚无标准治疗方法。我们首次报告了一名57岁、激素受体阴性、阳性的晚期乳腺癌女性,她对多线抗治疗耐药,通过二代测序(NGS)检测到扩增及突变。她随后接受了吡咯替尼联合卡培他滨治疗并获得部分缓解。小分子泛家族不可逆抑制剂吡咯替尼联合卡培他滨在治疗突变诱导的耐药方面已显示出有前景的效果,但分子机制和疗效有待进一步验证。