1st Department of Medical Oncology, Saint Savas Anticancer Hospital, 11522 Athens, Greece.
Department of Oncology, University Hospital of Larissa, 41221 Larissa, Greece.
Curr Oncol. 2022 Feb 17;29(2):1237-1251. doi: 10.3390/curroncol29020105.
Front-line bevacizumab (BEV) in combination with taxanes offers benefit in progression-free survival (PFS) in metastatic breast cancer (mBC). The medical records of mBC patients, treated with front-line BEV-based chemotherapy, were retrospectively reviewed in order to generate real life safety and efficacy data. Patients with human epidermal growth factor receptor 2 (HER2)-negative mBC treated with front-line BEV in combination with chemotherapy were eligible. Maintenance therapy with BEV and/or hormonal agents was at the physicians' discretion. Among the 387 included patients, the most common adverse events were anemia (61.9%, mainly grade 1), grade 3/4 neutropenia (16.5%), grade 1/2 fatigue (22.3%), and grade 1/2 neuropathy (19.6%). Dose reductions were required in 164 cycles (7.1%) and toxicity led to treatment discontinuation in 21 patients (5.4%). The median PFS and the median overall survival (OS) were 13.3 (95% CI: 11.7-14.8) and 32.3 months (95% CI: 27.7-36.9), respectively. Maintenance therapy, with hormonal agents (ET) and/or BEV, was associated with longer OS versus no maintenance therapy (47.2 versus 23.6 months; < 0.001) in patients with hormone receptor (HR)-positive disease and BEV maintenance offered longer OS versus no maintenance in patients with HR-negative disease (52.8 versus 23.3; = 0.023). These real-life data show that front-line BEV-based chemotherapy in HER2-negative mBC patients is an effective treatment with an acceptable toxicity profile. The potential benefit of maintenance treatment, especially ET, is important and warrants further research.
贝伐珠单抗(bevacizumab,BEV)联合紫杉烷类药物可改善转移性乳腺癌(mBC)患者的无进展生存期(progression-free survival,PFS)。本研究回顾性分析了接受一线 BEV 为基础的化疗治疗的 mBC 患者的病历资料,旨在生成真实世界的安全性和疗效数据。纳入标准为:HER2 阴性 mBC 患者,接受一线 BEV 联合化疗治疗。BEV 和/或激素维持治疗由医生决定。在 387 例纳入患者中,最常见的不良反应为贫血(61.9%,主要为 1 级)、3/4 级中性粒细胞减少症(16.5%)、1/2 级乏力(22.3%)和 1/2 级周围神经病变(19.6%)。需要减少剂量的周期有 164 个(7.1%),毒性导致 21 例患者(5.4%)停药。中位 PFS 和总生存期(overall survival,OS)分别为 13.3 个月(95%CI:11.7-14.8)和 32.3 个月(95%CI:27.7-36.9)。对于激素受体(hormone receptor,HR)阳性疾病患者,激素药物(endocrine therapy,ET)和/或 BEV 维持治疗可延长 OS(47.2 个月 vs. 23.6 个月;<0.001);对于 HR 阴性疾病患者,BEV 维持治疗可延长 OS(52.8 个月 vs. 23.3 个月;=0.023)。这些真实世界的数据表明,HER2 阴性 mBC 患者的一线 BEV 为基础的化疗是一种有效的治疗方法,具有可接受的毒性特征。维持治疗,尤其是 ET,具有潜在获益,值得进一步研究。