Division of Medical Senology, Istituto Europeo di Oncologia, IRCCS.
Department of Statistics and Quantitative Methods, University of Milan-Bicocca.
Anticancer Drugs. 2022 Jan 1;33(1):e628-e634. doi: 10.1097/CAD.0000000000001209.
Metronomic chemotherapy is a treatment option for metastatic breast cancer (MBC) patients who require prolonged disease control without cumulative toxicity. Data available on the efficacy and tolerability of prolonged usage of metronomic therapy are limited. We analyzed patients with MBC, enrolled in a clinical trial, who obtained a prolonged clinical benefit for a duration of at least 12 months with vinorelbine 30 or 40 mg orally three times a week, cyclophosphamide 50 mg daily and capecitabine 500 mg three times a day (VEX regimen). The patients were treated at the European Institute of Oncology, Milan. We identified 67 MBC patients. The median age before starting the VEX regimen was 53 years. There were 59 patients (88%) who had hormone-receptors positive and HER2 negative BC. We had 37 patients who received VEX as the first-line treatment for MBC, while 30 patients were pretreated. The objective response rate was 49% (95% CI, 37-62). The median duration of VEX treatment after the first year was 14 months (min-max range 0.3-81.3 months). The progression-free survival at 3 years was 25.4% (95% CI, 15.7-36.2) and at 4 years was 18.5% (95% CI, 10.1-28.8 time 0 corresponds to 1 year after starting VEX). A total of 25 patients required a dose reduction, 7% of patients experienced G3 hand and foot syndrome. Metronomic VEX regimen can induce prolonged clinical benefit in MBC. On the basis of this long-term safety evaluation, there is no evidence of specific cumulative or delayed toxicities with metronomic chemotherapy.
节拍化疗是一种治疗转移性乳腺癌(MBC)患者的选择,这些患者需要长期控制疾病而无累积毒性。关于节拍化疗延长使用的疗效和耐受性的数据有限。我们分析了在临床试验中接受治疗的 MBC 患者,这些患者接受每周三次口服长春瑞滨 30 或 40mg、环磷酰胺 50mg 每日和卡培他滨 500mg 每日三次(VEX 方案)治疗,持续至少 12 个月获得了延长的临床获益。这些患者在米兰的欧洲肿瘤研究所接受治疗。我们确定了 67 名 MBC 患者。开始 VEX 方案前的中位年龄为 53 岁。有 59 名患者(88%)为激素受体阳性和 HER2 阴性 BC。我们有 37 名患者将 VEX 作为 MBC 的一线治疗,而 30 名患者为预处理。客观缓解率为 49%(95%CI,37-62)。第一年之后 VEX 治疗的中位持续时间为 14 个月(最小-最大范围 0.3-81.3 个月)。3 年时无进展生存率为 25.4%(95%CI,15.7-36.2),4 年时为 18.5%(95%CI,10.1-28.8,时间 0 对应于开始 VEX 后 1 年)。共有 25 名患者需要减少剂量,7%的患者发生 G3 手足综合征。节拍 VEX 方案可在 MBC 中诱导延长的临床获益。基于这项长期安全性评估,节拍化疗没有累积或延迟毒性的证据。