Division of Pulmonary Medicine, Kobe City Medical Center General Hospital, Kobe, Japan.
Cancer. 2012 Dec 15;118(24):6126-35. doi: 10.1002/cncr.26689. Epub 2012 Jun 6.
This study sought to ascertain whether induction-concurrent radiotherapy added to chemotherapy could improve the survival of patients undergoing surgery for stage IIIA N2 nonsmall cell lung cancer (NSCLC).
Patients with pathologically proven N2 disease were randomized to receive either induction chemotherapy (docetaxel 60 mg/m(2) and carboplatin AUC [area under the receiver operating characteristic curve] = 5 for 2 cycles) plus concurrent radiation therapy (40 Gy) followed by surgery (CRS arm) or induction chemotherapy followed by surgery (CS arm). They subsequently underwent pulmonary resection when possible.
Sixty patients were randomly assigned between December 2000 and August 2005. The study was prematurely terminated in January 2006 because of slow accrual. The most common toxicity was grade 3 or 4 leukopenia in 92.9% of patients in the CRS arm and 46.4% in the CS arm. Induction therapy was generally well tolerated, and there were no treatment-related deaths in either arm. Downstaging in the CS arm and CRS arm was 21% and 40%, respectively. The progression-free survival (PFS) and overall survival (OS) in the CS arm were 9.7 months and 29.9 months (PFS, hazard ratio [HR] = 0.68, P = .187), and those in the CRS arm were 12.4 months and 39.6 months (OS, HR = 0.77, P = .397), respectively. The PFS with and without downstaging was 55.0 and 9.4 months, respectively (HR = 3.39, P = .001). The OS with and without downstaging was 63.3 and 29.5 months, respectively (HR = 2.62, P = .021).
The addition of radiotherapy to induction chemotherapy conferred better local control without significant adverse events. Tumor downstaging is important for prolonging the OS in patients with stage IIIA (N2) NSCLC.
本研究旨在确定诱导-同期放化疗联合化疗是否能改善 IIIA N2 期非小细胞肺癌(NSCLC)患者的生存。
经病理证实存在 N2 疾病的患者被随机分为接受诱导化疗(多西他赛 60mg/m2 和卡铂 AUC[受体操作特性曲线下面积]=5,共 2 个周期)联合同期放疗(40Gy)后手术(CRS 组)或诱导化疗后手术(CS 组)。如果可能,他们随后接受肺切除术。
2000 年 12 月至 2005 年 8 月期间共 60 例患者被随机分配。由于入组缓慢,该研究于 2006 年 1 月提前终止。CRS 组中 92.9%的患者和 CS 组中 46.4%的患者最常见的毒性为 3 或 4 级白细胞减少。诱导治疗通常耐受良好,两组均无治疗相关死亡。CS 组和 CRS 组的降期分别为 21%和 40%。CS 组的无进展生存期(PFS)和总生存期(OS)分别为 9.7 个月和 29.9 个月(PFS,风险比[HR] = 0.68,P =.187),CRS 组分别为 12.4 个月和 39.6 个月(OS,HR = 0.77,P =.397)。有和无降期的 PFS 分别为 55.0 和 9.4 个月(HR = 3.39,P =.001)。有和无降期的 OS 分别为 63.3 和 29.5 个月(HR = 2.62,P =.021)。
放疗联合诱导化疗可改善局部控制,且无显著不良反应。肿瘤降期对延长 IIIA(N2)期 NSCLC 患者的 OS 非常重要。