Hospital Universitario La Paz, 28046 Madrid, Spain.
Hospital Arnau de Vilanova de Lleida, 25198 Lleida, Spain.
Br J Cancer. 2014 Jul 15;111(2):241-8. doi: 10.1038/bjc.2014.346. Epub 2014 Jun 19.
Subgroup analyses of clinical studies suggest that bevacizumab plus XELOX is effective and tolerable in elderly patients with metastatic colorectal cancer (mCRC). The prospective BECOX study examined the efficacy and safety of bevacizumab plus XELOX, followed by bevacizumab plus capecitabine in elderly patients with mCRC.
Patients aged ⩾70 years with Eastern Cooperative Oncology Group performance status 0 out of 1 and confirmed mCRC were included. Patients received bevacizumab 7.5 mg kg(-1) and oxaliplatin 130 mg m(-2) on day 1, plus capecitabine 1000 mg m(-2) bid orally on days 1-14 every 21 days; oxaliplatin was discontinued after 6 cycles. The primary end point was time to progression (TTP).
The intent-to-treat population comprised 68 patients (65% male, median age 76 years). Median TTP was 11.1 months; median overall survival was 20.4 months; overall response rate was 46%. Grade 3 or 4 adverse events included diarrhoea (18%) and asthenia (16%). Grade 3 or 4 adverse events of special interest for bevacizumab included deep-vein thrombosis (6%) and pulmonary embolism (4%).
Bevacizumab plus XELOX was effective and well tolerated in elderly patients in the BECOX study. The adverse-event profile was similar to previous reports; no new safety concerns were identified. Fit elderly patients with mCRC should be considered for treatment with bevacizumab plus XELOX.
临床研究的亚组分析表明,贝伐珠单抗联合 XELOX 方案在转移性结直肠癌(mCRC)老年患者中是有效且耐受良好的。前瞻性 BECOX 研究评估了贝伐珠单抗联合 XELOX 方案,随后贝伐珠单抗联合卡培他滨在 mCRC 老年患者中的疗效和安全性。
纳入年龄 ⩾70 岁、东部肿瘤协作组体力状态 0 分且确诊为 mCRC 的患者。患者接受贝伐珠单抗 7.5 mg/kg 和奥沙利铂 130 mg/m²,第 1 天静脉滴注,卡培他滨 1000 mg/m²,bid,口服,第 1-14 天,每 21 天为 1 个周期;6 个周期后停用奥沙利铂。主要终点为无进展生存期(TTP)。
意向治疗人群包括 68 例患者(65%为男性,中位年龄 76 岁)。中位 TTP 为 11.1 个月;中位总生存期为 20.4 个月;总缓解率为 46%。3 级或 4 级不良事件包括腹泻(18%)和乏力(16%)。贝伐珠单抗相关 3 级或 4 级特殊关注的不良事件包括深静脉血栓形成(6%)和肺栓塞(4%)。
贝伐珠单抗联合 XELOX 在 BECOX 研究中对老年患者是有效且耐受良好的。不良事件谱与既往报告相似;未发现新的安全性问题。适合治疗的老年 mCRC 患者应考虑采用贝伐珠单抗联合 XELOX 方案。