Department of Respiratory Medicine, Graduate School of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.
Cancer Chemother Pharmacol. 2012 Aug;70(2):271-6. doi: 10.1007/s00280-012-1910-2. Epub 2012 Jun 30.
Subgroup analyses of randomized studies have consistently shown that pemetrexed is exclusively effective in non-small-cell lung cancer (NSCLC) other than squamous cell carcinoma and the combination of pemetrexed and platinum agents is recommended for first-line chemotherapy in advanced non-squamous NSCLC; however, there have been few prospective studies of a selected population.
This was a single-arm phase II study of carboplatin and pemetrexed in Japanese patients with chemo-naive advanced non-squamous NSCLC. Patients received six cycles of pemetrexed (500 mg/m(2)) combined with carboplatin (area under the curve: AUC 6) every 3 weeks. Maintenance chemotherapy with pemetrexed was permitted in patients whose disease did not progress after combination chemotherapy. The primary endpoint was the response rate, and secondary endpoints were safety and survival.
Fifty-one patients were enrolled between November 2009 and March 2011, and 49 patients were evaluable for both safety and efficacy. All but one patient had adenocarcinoma histology. Forty-four (90 %) patients completed four cycles, and 33 (67 %) completed six cycles of chemotherapy. Partial response was achieved in 25 patients (response rate: 51 %) and stable disease in 18 patients (37 %). Median progression-free survival (PFS) and overall survival (OS) were 6.3 months and 24.3 months, respectively. The median PFS and OS were 7.9 months and 24.3 months in patients with epidermal growth factor receptor (EGFR) mutation, and 6.3 months and 21.0 months in patients with EGFR wild type or unknown. There were no statistical differences between EGFR mutants and non-mutants for both PFS (p = 0.09) and OS (p = 0.23). Grade 3/4 neutropenia and thrombocytopenia were observed in 16 (33 %) and 9 (18 %) patients, respectively. Non-hematologic toxicities were generally mild, and there were no treatment-related deaths.
The combination of carboplatin and pemetrexed was safe and effective in advanced non-squamous NSCLC. Although the sample size was small, our results indicate that pemetrexed is a key drug for advanced non-squamous NSCLC, irrespective of the EGFR mutation status (UMIN-CTR number 000002451).
随机研究的亚组分析一致表明,培美曲塞仅对非鳞状非小细胞肺癌(NSCLC)有效,而非鳞状细胞癌,培美曲塞联合铂类药物被推荐用于晚期非鳞状 NSCLC 的一线化疗;然而,对于选定人群的前瞻性研究很少。
这是一项在日本未经化疗的晚期非鳞状 NSCLC 患者中进行的卡铂和培美曲塞单臂 II 期研究。患者每 3 周接受 6 个周期的培美曲塞(500mg/m2)联合卡铂(曲线下面积:AUC 6)。联合化疗后疾病未进展的患者可接受培美曲塞维持化疗。主要终点为缓解率,次要终点为安全性和生存。
2009 年 11 月至 2011 年 3 月期间,共纳入 51 例患者,49 例患者可评估疗效和安全性。所有患者均为腺癌组织学。44 例(90%)患者完成了 4 个周期的化疗,33 例(67%)患者完成了 6 个周期的化疗。25 例患者(缓解率:51%)获得部分缓解,18 例(37%)患者疾病稳定。中位无进展生存期(PFS)和总生存期(OS)分别为 6.3 个月和 24.3 个月。表皮生长因子受体(EGFR)突变患者的中位 PFS 和 OS 分别为 7.9 个月和 24.3 个月,EGFR 野生型或未知患者的中位 PFS 和 OS 分别为 6.3 个月和 21.0 个月。在 PFS(p=0.09)和 OS(p=0.23)方面,EGFR 突变与非突变患者之间均无统计学差异。16 例(33%)患者出现 3/4 级中性粒细胞减少,9 例(18%)患者出现血小板减少。非血液学毒性通常较轻,无治疗相关死亡。
卡铂联合培美曲塞治疗晚期非鳞状 NSCLC 安全有效。尽管样本量较小,但我们的结果表明,培美曲塞是晚期非鳞状 NSCLC 的关键药物,与 EGFR 突变状态无关(UMIN-CTR 编号 000002451)。