Strauss Gary M, Herndon James E, Maddaus Michael A, Johnstone David W, Johnson Elizabeth A, Harpole David H, Gillenwater Heidi H, Watson Dorothy M, Sugarbaker David J, Schilsky Richard L, Vokes Everett E, Green Mark R
Tufts Medical Center, Division of Medical Oncology, Tufts-NEMC, Boston, MA 02111, USA.
J Clin Oncol. 2008 Nov 1;26(31):5043-51. doi: 10.1200/JCO.2008.16.4855. Epub 2008 Sep 22.
Adjuvant chemotherapy for resected non-small-cell lung cancer (NSCLC) is now accepted on the basis of several randomized clinical trials (RCTs) that demonstrated improved survival. Although there is strong evidence that adjuvant chemotherapy is effective in stages II and IIIA NSCLC, its utility in stage IB disease is unclear. This report provides a mature analysis of Cancer and Leukemia Group B (CALGB) 9633, the only RCT designed specifically for stage IB NSCLC.
Within 4 to 8 weeks of resection, patients were randomly assigned to adjuvant chemotherapy or observation. Eligible patients had pathologically confirmed T2N0 NSCLC and had undergone lobectomy or pneumonectomy. Chemotherapy consisted of paclitaxel 200 mg/m(2) intravenously over 3 hours and carboplatin at an area under the curve dose of 6 mg/mL per minute intravenously over 45 to 60 minutes every 3 weeks for four cycles. The primary end point was overall survival.
Three hundred-forty-four patients were randomly assigned. Median follow-up was 74 months. Groups were well-balanced with regard to demographics, histology, and extent of surgery. Grades 3 to 4 neutropenia were the predominant toxicity; there were no treatment-related deaths. Survival was not significantly different (hazard ratio [HR], 0.83; CI, 0.64 to 1.08; P = .12). However, exploratory analysis demonstrated a significant survival difference in favor of adjuvant chemotherapy for patients who had tumors > or = 4 cm in diameter (HR, 0.69; CI, 0.48 to 0.99; P = .043).
Because a significant survival advantage was not observed across the entire cohort, adjuvant chemotherapy should not be considered standard care in stage IB NSCLC. Given the magnitude of observed survival differences, CALGB 9633 was underpowered to detect small but clinically meaningful improvements. A statistically significant survival advantage for patients who had tumors > or = 4 cm supports consideration of adjuvant paclitaxel/carboplatin for stage IB patients who have large tumors.
基于多项显示生存期改善的随机临床试验(RCT),辅助化疗现已被用于已切除的非小细胞肺癌(NSCLC)。尽管有强有力的证据表明辅助化疗对II期和IIIA期NSCLC有效,但其在IB期疾病中的效用尚不清楚。本报告对癌症与白血病B组(CALGB)9633进行了成熟分析,这是唯一一项专门为IB期NSCLC设计的RCT。
在切除术后4至8周内,患者被随机分配接受辅助化疗或观察。符合条件的患者经病理证实为T2N0 NSCLC,且已接受肺叶切除术或全肺切除术。化疗方案为每3周静脉输注紫杉醇200mg/m²,持续3小时,同时静脉输注卡铂,曲线下面积剂量为6mg/mL每分钟,持续45至60分钟,共四个周期。主要终点为总生存期。
344例患者被随机分配。中位随访时间为74个月。两组在人口统计学、组织学和手术范围方面均衡良好。3至4级中性粒细胞减少是主要毒性反应;无治疗相关死亡。生存期无显著差异(风险比[HR],0.83;可信区间[CI],0.64至1.08;P = 0.12)。然而,探索性分析显示,对于肿瘤直径≥4cm的患者,辅助化疗有显著的生存差异(HR,0.69;CI,0.48至0.99;P = 0.043)。
由于在整个队列中未观察到显著的生存优势,辅助化疗不应被视为IB期NSCLC的标准治疗。鉴于观察到的生存差异程度,CALGB 9633检测小但具有临床意义的改善功效不足。对于肿瘤直径≥4cm的患者,统计学上显著的生存优势支持考虑对IB期大肿瘤患者采用辅助紫杉醇/卡铂治疗。