Randomized Phase III Trial of Vinorelbine Plus Cisplatin Compared With Observation in Completely Resected Stage IB and II Non-Small-Cell Lung Cancer: Updated Survival Analysis of JBR-10

被引:323
作者
Butts, Charles A. [1 ]
Ding, Keyue
Seymour, Lesley
Twumasi-Ankrah, Philip
Graham, Barbara
Gandara, David
Johnson, David H.
Kesler, Kenneth A.
Green, Mark
Vincent, Mark
Cormier, Yvon
Goss, Glenwood
Findlay, Brian
Johnston, Michael
Tsao, Ming-Sound
Shepherd, Frances A.
机构
[1] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
关键词
B CALGB PROTOCOL-9633; ADJUVANT CHEMOTHERAPY; COMORBIDITY; THERAPY; SMOKING; NSCLC;
D O I
10.1200/JCO.2009.24.0333
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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.
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页码:29 / 34
页数:6
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