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一线贝伐珠单抗联合化疗加或不加维持治疗转移性乳腺癌:希腊肿瘤研究组的一项观察性研究。

Front-Line Bevacizumab plus Chemotherapy with or without Maintenance Therapy for Metastatic Breast Cancer: An Observational Study by the Hellenic Oncology Research Group.

机构信息

1st Department of Medical Oncology, Saint Savas Anticancer Hospital, 11522 Athens, Greece.

Department of Oncology, University Hospital of Larissa, 41221 Larissa, Greece.

出版信息

Curr Oncol. 2022 Feb 17;29(2):1237-1251. doi: 10.3390/curroncol29020105.

DOI:10.3390/curroncol29020105
PMID:35200604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8871254/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/a6e5c2a9e30e/curroncol-29-00105-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/a339790912df/curroncol-29-00105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/dd5a1451c758/curroncol-29-00105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/ca1028dd8bcb/curroncol-29-00105-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/62c4744a83d8/curroncol-29-00105-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/a6e5c2a9e30e/curroncol-29-00105-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/a339790912df/curroncol-29-00105-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/dd5a1451c758/curroncol-29-00105-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/ca1028dd8bcb/curroncol-29-00105-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/62c4744a83d8/curroncol-29-00105-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dacb/8871254/a6e5c2a9e30e/curroncol-29-00105-g005.jpg

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