Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, Japan.
Cancer Chemother Pharmacol. 2013 Aug;72(2):445-52. doi: 10.1007/s00280-013-2218-6. Epub 2013 Jun 27.
The optimal strategy for maintenance chemotherapy is controversial. We evaluated the efficacy and safety of continuation maintenance with pemetrexed and switch maintenance with docetaxel in advanced non-squamous non-small-cell lung cancer (NSCLC).
Chemotherapy-naïve patients with non-squamous NSCLC were enrolled in this randomized phase II study. Patients who achieved disease control after four cycles of induction therapy with carboplatin (AUC 6) and pemetrexed (500 mg/m(2)) were randomized to maintenance therapy with pemetrexed (500 mg/m(2)) or docetaxel (60 mg/m(2)). The primary endpoint was survival without toxicity, defined as the time from the initiation of maintenance therapy to the first date of any grade 3/4 toxicity or death due to any cause.
A total of eighty-five patients were enrolled in the induction phase, and 26 patients were assigned to the pemetrexed maintenance therapy and 25 patients were assigned to the docetaxel maintenance therapy. Survival without toxicity was significantly longer in the pemetrexed group (median 20.8 months, 95 % confidence interval (CI) 0.7-not estimable) than in the docetaxel group (median 0.5 months, 95 % CI 0.2-2.0, hazard ratio 0.36, 95 % CI 0.17-0.74).
Continuation maintenance with pemetrexed may be a feasible treatment option for patients with non-squamous NSCLC who have achieved disease control after induction therapy with carboplatin and pemetrexed. Switch maintenance with docetaxel may also be efficacious but frequently causes severe hematologic toxicity.
维持化疗的最佳策略仍存在争议。我们评估了培美曲塞延续维持治疗和多西他赛转换维持治疗在晚期非鳞状非小细胞肺癌(NSCLC)中的疗效和安全性。
本随机Ⅱ期研究纳入了化疗初治的非鳞状 NSCLC 患者。在接受卡铂(AUC 6)和培美曲塞(500mg/m²)诱导治疗 4 个周期后达到疾病控制的患者被随机分配至培美曲塞(500mg/m²)或多西他赛(60mg/m²)维持治疗。主要终点为无毒性生存,定义为从维持治疗开始至因任何原因发生任何 3/4 级毒性或死亡的首次日期的时间。
共有 85 例患者入组诱导治疗阶段,26 例患者被分配至培美曲塞维持治疗组,25 例患者被分配至多西他赛维持治疗组。培美曲塞组的无毒性生存时间明显长于多西他赛组(中位 20.8 个月,95%置信区间 0.7-无法估计)(中位 0.5 个月,95%置信区间 0.2-2.0,风险比 0.36,95%置信区间 0.17-0.74)。
在接受卡铂和培美曲塞诱导治疗后疾病控制的非鳞状 NSCLC 患者中,培美曲塞延续维持治疗可能是一种可行的治疗选择。多西他赛转换维持治疗也可能有效,但常导致严重的血液学毒性。