Sargent Daniel J, Patiyil Smitha, Yothers Greg, Haller Daniel G, Gray Richard, Benedetti Jacqueline, Buyse Marc, Labianca Roberto, Seitz Jean Francois, O'Callaghan Christopher J, Francini Guido, Grothey Axel, O'Connell Michael, Catalano Paul J, Kerr David, Green Erin, Wieand Harry S, Goldberg Richard M, de Gramont Aimery
Department of Health Sciences Research, North Central Cancer Treatment Group, Mayo Clinic, Rochester, MN 55905, USA.
J Clin Oncol. 2007 Oct 10;25(29):4569-74. doi: 10.1200/JCO.2006.10.4323. Epub 2007 Sep 17.
The traditional end point for colon adjuvant clinical trials is overall survival (OS). We previously validated disease-free survival (DFS) after 3-year follow-up as an excellent predictor of 5-year OS results. Here we explore shorter term DFS and OS end points, as well as stage dependency.
Individual patient data from 18 phase III trials including 43 arms and 20,898 patients were pooled. Association measures included correlation of event rates within arms, correlation of hazard ratios (HRs) between arms, trial level significance comparisons (via log-rank testing), and a formal surrogacy model.
DFS at earlier times was less accurate in predicting OS than 3-year DFS, but 2-year DFS remained a strong predictor. DFS with 1-year minimum follow-up demonstrated perfect negative predicted value; all trials negative at 1 year for DFS were negative for 5-year OS. OS with 3-year minimum follow-up was also an excellent predictor for 5-year OS; OS at earlier time points provided inaccurate prediction. The association between 3-year DFS and 5-year OS was greater for stage III patients; correlation of HR within trials was 0.92 (95% CI, 0.85 to 0.95) for stage III patients and 0.70 (95% CI, 0.44 to 0.80) for stage II patients.
DFS outcomes after 2- or 3-year median follow-up are excellent predictors of 5-year OS. DFS outcomes are appropriate for trials in which the majority of patients are stage III. DFS after 2- or 3-year median follow-up should be considered as the primary end point in future colon adjuvant trials.
结肠癌辅助临床试验的传统终点是总生存期(OS)。我们之前验证了3年随访后的无病生存期(DFS)是5年OS结果的优秀预测指标。在此,我们探讨更短期的DFS和OS终点,以及分期依赖性。
汇总了来自18项III期试验的个体患者数据,包括43个治疗组和20898例患者。关联测量包括各治疗组内事件发生率的相关性、各治疗组间风险比(HRs)的相关性、试验水平的显著性比较(通过对数秩检验)以及一个正式的替代模型。
早期的DFS在预测OS方面不如3年DFS准确,但2年DFS仍是一个强有力的预测指标。至少随访1年的DFS显示出完美的阴性预测值;所有1年时DFS为阴性的试验,其5年OS也为阴性。至少随访3年的OS也是5年OS的优秀预测指标;早期时间点的OS预测不准确。III期患者中3年DFS与5年OS之间的关联更强;III期患者试验内HR的相关性为0.92(95%CI,0.85至0.95),II期患者为0.70(95%CI,0.44至0.80)。
中位随访2年或3年后的DFS结果是5年OS的优秀预测指标。DFS结果适用于大多数患者为III期的试验。中位随访2年或3年后的DFS应被视为未来结肠癌辅助试验的主要终点。