Cross Cancer Institute, 11560 University Ave, Edmonton, Alberta, Canada, T6G 1Z2.
J Clin Oncol. 2010 Jan 1;28(1):29-34. doi: 10.1200/JCO.2009.24.0333. Epub 2009 Nov 23.
PURPOSE Adjuvant cisplatin-based chemotherapy (ACT) is now an accepted standard for completely resected stage II and III A non-small-cell lung cancer (NSCLC). Long-term follow-up is important to document persistent benefit and late toxicity. We report here updated overall survival (OS) and disease-specific survival (DSS) data. PATIENTS AND METHODS Patients with completely resected stage IB (T2N0, n = 219) or II (T1-2N1, n = 263) NSCLC were randomly assigned to receive 4 cycles of vinorelbine/cisplatin or observation. All efficacy analyses were performed on an intention-to-treat basis. Results Median follow-up was 9.3 years (range, 5.8 to 13.8; 33 lost to follow-up); there were 271 deaths in 482 randomly assigned patients. ACT continues to show a benefit (hazard ratio [HR], 0.78; 95% CI, 0.61 to 0.99; P = .04). There was a trend for interaction with disease stage (P = .09; HR for stage II, 0.68; 95% CI, 0.5 to 0.92; P = .01; stage IB, HR, 1.03; 95% CI, 0.7 to 1.52; P = .87). ACT resulted in significantly prolonged DSS (HR, 0.73; 95% CI, 0.55 to 0.97; P = .03). Observation was associated with significantly higher risk of death from lung cancer (P = .02), with no difference in rates of death from other causes or second primary malignancies between the arms. CONCLUSION Prolonged follow-up of patients from the JBR.10 trial continues to show a benefit in survival for adjuvant chemotherapy. This benefit appears to be confined to N1 patients. There was no increase in death from other causes in the chemotherapy arm.
辅助顺铂为基础的化疗(ACT)目前被公认为完全切除的 II 期和 IIIA 期非小细胞肺癌(NSCLC)的标准治疗方法。长期随访对于证明持续获益和晚期毒性非常重要。我们在此报告更新的总生存(OS)和疾病特异性生存(DSS)数据。
完全切除的 I 期 B(T2N0,n = 219)或 II 期(T1-2N1,n = 263)NSCLC 患者被随机分配接受 4 个周期的长春瑞滨/顺铂或观察。所有疗效分析均基于意向治疗进行。
中位随访时间为 9.3 年(范围,5.8 至 13.8;33 例失访);482 例随机分配患者中有 271 例死亡。ACT 继续显示出获益(风险比[HR],0.78;95%CI,0.61 至 0.99;P =.04)。与疾病分期存在趋势性交互作用(P =.09;II 期 HR,0.68;95%CI,0.5 至 0.92;P =.01;I B 期 HR,1.03;95%CI,0.7 至 1.52;P =.87)。ACT 显著延长了 DSS(HR,0.73;95%CI,0.55 至 0.97;P =.03)。观察与肺癌死亡风险显著增加相关(P =.02),但两组之间其他原因死亡或第二原发恶性肿瘤的发生率无差异。
JBR.10 试验患者的长期随访继续显示辅助化疗在生存方面的获益。这种获益似乎仅限于 N1 患者。化疗组没有因其他原因导致的死亡增加。