Washington University School of Medicine, 4960 Children's Place, St Louis, MO 63110, USA.
J Clin Oncol. 2011 Aug 10;29(23):3120-5. doi: 10.1200/JCO.2010.33.4979. Epub 2011 Jul 11.
Cancer and Leukemia Group B conducted a randomized phase II trial to investigate two novel chemotherapy regimens in combination with concurrent thoracic radiation therapy (TRT).
Patients with unresectable stage III non-small-cell lung cancer (NSCLC) were randomly assigned to carboplatin (area under the curve, 5) and pemetrexed (500 mg/m(2)) every 21 days for four cycles and TRT (70 Gy; arm A) or the same treatment with cetuximab administered concurrent only with TRT (arm B). Patients in both arms received up to four cycles of pemetrexed as consolidation therapy. The primary end point was the 18-month overall survival (OS) rate; if the 18-month OS rate was ≥ 55%, the regimen(s) would be considered for further study.
Of the 101 eligible patients enrolled (48 in arm A and 53 in arm B), 60% were male; the median age was 66 years (range, 32 to 81 years); 44% and 35% had adenocarcinoma and squamous carcinoma, respectively; and more patients enrolled onto arm A compared with arm B had a performance status of 0 (58% v 34%, respectively; P = .04). The 18-month OS rate was 58% (95% CI, 46% to 74%) in arm A and 54% (95% CI, 42% to 70%) in arm B. No significant difference in OS between patients with squamous and nonsquamous NSCLC was observed (P = .667). The toxicities observed were consistent with toxicities associated with concurrent chemoradiotherapy.
The combination of pemetrexed, carboplatin, and TRT met the prespecified criteria for further evaluation. This regimen should be studied further in patients with locally advanced unresectable nonsquamous NSCLC.
癌症和白血病小组 B 进行了一项随机的 II 期试验,旨在研究两种新型化疗方案联合同期胸部放射治疗 (TRT) 的效果。
无法切除的 III 期非小细胞肺癌 (NSCLC) 患者被随机分配至卡铂(曲线下面积 5)和培美曲塞(500mg/m²)每 21 天给药 4 个周期联合 TRT(70Gy;A 组),或相同治疗方案联合仅在 TRT 时使用西妥昔单抗(B 组)。两组患者均接受最多 4 个周期的培美曲塞巩固治疗。主要终点是 18 个月总生存(OS)率;如果 18 个月 OS 率≥55%,则认为该方案(们)值得进一步研究。
共纳入 101 例符合条件的患者(A 组 48 例,B 组 53 例),其中 60%为男性;中位年龄为 66 岁(范围 32-81 岁);44%和 35%分别为腺癌和鳞状细胞癌;与 B 组相比,更多的 A 组患者的体能状态为 0(分别为 58%和 34%;P=0.04)。A 组的 18 个月 OS 率为 58%(95%CI,46%-74%),B 组为 54%(95%CI,42%-70%)。未观察到鳞状细胞癌和非鳞状细胞癌患者之间的 OS 存在显著差异(P=0.667)。观察到的毒性与同期放化疗相关的毒性一致。
培美曲塞、卡铂和 TRT 的联合符合进一步评估的预设标准。该方案应在局部晚期不可切除的非鳞状 NSCLC 患者中进一步研究。