Department of Breast disease, Henan Breast Cancer Center, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, Henan Province, China.
Deprtment of Ultrasonography, Fudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
J Cell Mol Med. 2024 Mar;28(5):e18008. doi: 10.1111/jcmm.18008. Epub 2023 Oct 27.
Anlotinib, a multitarget tyrosine kinase inhibitor, can inhibit tumour angiogenesis proliferation, metastasis, promote vascular normalization, increase T cell and NK cell activity and infiltration, remodel tumour microenvironment and synergistic immune enhancement. Our study aimes to evaluate the efficacy of anlotinib in the treatment of advanced metastatic breast cancer (MBC) after multiple lines of therapy. Patients included were treated with anlotinib for advanced MBC in the Affiliated Cancer Hospital of Zhengzhou University from 1 January 2019 to 30 June 2023. The objective remission rate, disease-free progression survival and adverse reactions were analysed. We compared and analysed the efficacy of anlotinib in the treatment of advanced metastatic breast cancer, which showed that ORR was 23.6% and DCR was 69.1%. The DCR of monotherapy was 66.7% and that of combination therapy was 69.6% in MBC patients. The combination therapy, combined with chemotherapy had the best effect (79.3%), combined with immunotherapy came second. In addition, the DCR (88.9%) was higher in MBC patients having received prior antiangiogenic therapy. According to the Kaplan-Meier (K-M) survival estimate analysis, the mPFS was 4.17 months (95% CI, 1.758-6.582 months) in Her-2 positive MBC patients, and 7.83 months (95% CI, 2.416-9.104) in Her-2 negative MBC patients. The mPFS was 5.76 months (95% CI, 3.231-8.298 m) in HR positive MBC patients, 7.83 months (95% CI, 3.182-12.478 m) in TNBC patients. Fatigue (20.0%), hypertension (21.8%) and liver dysfunction (18.2%) were common adverse reactions, followed by bone marrow suppression (16.4%), anorexia (14.5%), hypothyroidism (14.5%) and diarrhoea (14.5%). Altogether, Anlotinib monotherapy or combination therapy provides a viable third (or above)-line therapeutic strategy in patients with metastatic breast cancer. The adverse reactions of anlotinib are well tolerated and controllable.
安罗替尼是一种多靶点酪氨酸激酶抑制剂,能够抑制肿瘤血管生成、增殖、转移,促进血管正常化,增加 T 细胞和 NK 细胞活性和浸润,重塑肿瘤微环境,协同增强免疫。本研究旨在评估安罗替尼治疗多线治疗后的晚期转移性乳腺癌(MBC)的疗效。入组患者为 2019 年 1 月 1 日至 2023 年 6 月 30 日在郑州大学附属肿瘤医院接受安罗替尼治疗的晚期 MBC 患者。分析客观缓解率(ORR)、无进展生存时间(PFS)和不良反应。比较分析安罗替尼治疗晚期转移性乳腺癌的疗效,结果显示,ORR 为 23.6%,疾病控制率(DCR)为 69.1%。单药治疗的 DCR 为 66.7%,联合治疗的 DCR 为 69.6%。联合化疗的效果最好(79.3%),联合免疫治疗次之。此外,有抗血管生成治疗史的 MBC 患者 DCR (88.9%)更高。根据 Kaplan-Meier(K-M)生存估计分析,Her-2 阳性 MBC 患者的 mPFS 为 4.17 个月(95%CI:1.758-6.582 个月),Her-2 阴性 MBC 患者为 7.83 个月(95%CI:2.416-9.104 个月)。HR 阳性 MBC 患者的 mPFS 为 5.76 个月(95%CI:3.231-8.298 个月),TNBC 患者为 7.83 个月(95%CI:3.182-12.478 个月)。常见不良反应为疲劳(20.0%)、高血压(21.8%)和肝功能异常(18.2%),其次为骨髓抑制(16.4%)、食欲下降(14.5%)、甲状腺功能减退(14.5%)和腹泻(14.5%)。总之,安罗替尼单药或联合治疗可为转移性乳腺癌患者提供可行的三线(或以上)治疗策略。安罗替尼的不良反应可耐受且可控制。