Department of Pharmacy, Gifu University Hospital, Gifu, Japan.
Department of Surgical Oncology, Gifu University Graduate School of Medicine, Gifu, Japan.
Oncologist. 2020 Mar;25(3):e469-e476. doi: 10.1634/theoncologist.2019-0541. Epub 2019 Nov 20.
TAS-102 is effective for treating patients with metastatic colorectal cancer (mCRC). This study determined whether combining bevacizumab (Bmab) with TAS-102 improves clinical outcomes in refractory mCRC.
We retrospectively analyzed data from Japanese patients with refractory mCRC who received TAS-102 (35 mg/m , twice a day) with (T-B group) or without Bmab (TAS-102 monotherapy; T group) between July 2014 and December 2018. The primary endpoint was median overall survival (OS), and secondary endpoints were median time to treatment failure, overall response rate, and the incidence of adverse events. Clinical outcomes were compared using propensity score matched analysis.
Data from 57 patients were analyzed (T-B group: 21 patients, T group: 36 patients). Median OS was significantly longer in the T-B group than the T group (14.4 months vs. 4.5 months, p < .001). Cox proportional hazard analysis showed that combination therapy with Bmab was significantly correlated with OS. Propensity score matched analysis confirmed that the median OS was significantly longer in the T-B group than the T group (14.4 months vs. 6.1 months, p = .006) and that there was a significant correlation between Bmab and OS. The incidence of hypertension (grade ≥2) as an adverse event was significantly higher in the T-B group than the T group (23.8% vs. 0.0%, p = .005), whereas other adverse events were comparable between the two groups.
Treatment with Bmab in combination with TAS-102 is significantly associated with improved clinical outcomes in patients with mCRC refractory to standard therapies.
Combining bevacizumab (Bmab) with TAS-102 significantly improved overall survival and several prognostic indicators in patients with metastatic colorectal cancer (mCRC) refractory to standard therapies, with manageable toxicities. Treatment with Bmab in combination with TAS-102 is significantly associated with improved clinical outcomes in patients with mCRC.
TAS-102 可有效治疗转移性结直肠癌(mCRC)患者。本研究旨在确定贝伐珠单抗(Bmab)联合 TAS-102 是否能改善难治性 mCRC 患者的临床结局。
我们回顾性分析了 2014 年 7 月至 2018 年 12 月期间接受 TAS-102(35mg/m²,每日 2 次)联合(T-B 组)或不联合 Bmab(TAS-102 单药治疗;T 组)治疗的难治性 mCRC 日本患者的数据。主要终点为中位总生存期(OS),次要终点为中位无进展生存期、总缓解率和不良事件发生率。采用倾向评分匹配分析比较临床结局。
共分析了 57 例患者的数据(T-B 组:21 例,T 组:36 例)。T-B 组的中位 OS 明显长于 T 组(14.4 个月 vs. 4.5 个月,p<0.001)。Cox 比例风险分析显示,Bmab 联合治疗与 OS 显著相关。倾向评分匹配分析证实,T-B 组的中位 OS 明显长于 T 组(14.4 个月 vs. 6.1 个月,p=0.006),Bmab 与 OS 显著相关。T-B 组高血压(≥2 级)的发生率明显高于 T 组(23.8% vs. 0.0%,p=0.005),而两组其他不良事件发生率相当。
Bmab 联合 TAS-102 治疗可显著改善标准治疗难治性 mCRC 患者的临床结局。
贝伐珠单抗(Bmab)联合 TAS-102 治疗标准治疗难治性转移性结直肠癌(mCRC)患者,可显著提高总生存率和多个预后指标,且毒性可耐受。Bmab 联合 TAS-102 治疗可显著改善难治性 mCRC 患者的临床结局。