Department of Oncology, Mayo Clinic, Rochester, Minnesota 55905, USA.
Cancer. 2010 May 15;116(10):2382-9. doi: 10.1002/cncr.24967.
In extensive-stage small cell lung cancer (SCLC), the combination of pemetrexed plus carboplatin has shown activity and appeared to be well-tolerated. We conducted a trial to confirm the efficacy and to assess the tolerability of this chemotherapy combination.
Patients with untreated extensive-stage SCLC were enrolled in this phase 2 open-labeled study. They receive pemetrexed 500 mg/m(2) and carboplatin (area under the curve of 5) every 21 days for a maximum 6 cycles. The primary endpoint for this trial was the confirmed response rate and the accrual goal was 70 patients.
Forty-six eligible patients (29 aged <70 years, 17 aged >or=70 years) were accrued to this study. The efficacy outcomes were similar between the 2 age groups. Overall, the confirmed response rate was 35% (16 of 46; 95% confidence interval [CI], 21%-50%), where all 16 were partial responses. On the basis of these results, we had strong evidence that the study would not meet the preset efficacy criteria and was, therefore, closed before full accrual. The median duration of response was 4.4 months (95% CI, 2.9-5.2). Median overall survival for patients aged <70 years and aged >or=70 years was 9.2 months (95% CI, 5.4-11.6) and 10.8 months (95% CI, 2.2-14.3), respectively. Grade 3 or higher toxicity rates were similar between the younger and older patients. Grade 3/4 and grade 4 hematological toxicities were observed in 46% and 26% of patients, respectively.
Although well-tolerated, the combination of pemetrexed and carboplatin is not as effective as standard therapy in patients with untreated extensive-stage SCLC.
在广泛期小细胞肺癌(SCLC)中,培美曲塞联合卡铂显示出了疗效,且耐受性良好。我们进行了一项试验以确认这种化疗联合方案的疗效和可耐受性。
这项 2 期、开放性标签研究纳入了未经治疗的广泛期 SCLC 患者。他们接受培美曲塞 500mg/m²和卡铂(曲线下面积 5)每 21 天 1 次,最多 6 个周期。该试验的主要终点为确认缓解率,入组目标为 70 例患者。
本研究共入组 46 例符合条件的患者(年龄<70 岁 29 例,年龄≥70 岁 17 例)。2 个年龄组的疗效结果相似。总体而言,确认缓解率为 35%(46 例患者中 16 例;95%置信区间[CI],21%50%),所有患者均为部分缓解。基于这些结果,我们有充分证据表明该研究不会达到预设的疗效标准,因此在完全入组前提前关闭。缓解持续时间的中位数为 4.4 个月(95%CI,2.95.2)。年龄<70 岁和年龄≥70 岁的患者中位总生存期分别为 9.2 个月(95%CI,5.411.6)和 10.8 个月(95%CI,2.214.3)。年轻患者和老年患者的 3/4 级及 4 级毒性发生率相似。分别有 46%和 26%的患者发生 3/4 级和 4 级血液学毒性。
培美曲塞联合卡铂虽然耐受性良好,但在未经治疗的广泛期 SCLC 患者中的疗效不如标准治疗。