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接受细胞毒性辅助治疗的结肠癌患者在复发后生存时间延长时,无病生存率和总生存率之间的关系:基于 20800 例患者 ACCENT 数据集的模拟。

Association between disease-free survival and overall survival when survival is prolonged after recurrence in patients receiving cytotoxic adjuvant therapy for colon cancer: simulations based on the 20,800 patient ACCENT data set.

机构信息

Hopital Saint Antoine, Group Hospitalier Pitie-Salpetriere, Paris, France.

出版信息

J Clin Oncol. 2010 Jan 20;28(3):460-5. doi: 10.1200/JCO.2009.23.1407. Epub 2009 Dec 14.

Abstract

PURPOSE

We previously validated disease-free survival (DFS) as a surrogate for overall survival (OS) in fluorouracil-based adjuvant colon cancer clinical trials. New therapies have extended survival after recurrence from 1 to approximately 2 years. We examined the possible impact of this improvement on the DFS/OS association.

METHODS

The Adjuvant Colon Cancer Endpoints (ACCENT) data set of 20,898 patients was analyzed. In an exploratory fashion, time from recurrence to death in patients experiencing recurrence was extended using several algorithms, and the association of DFS after 3 years of median follow-up and OS after varying lengths of follow-up (median of 5, 6, and 7 years) was assessed.

RESULTS

Seven thousand four hundred two patients (35%) experienced recurrence. Median time from recurrence to death was 24 months in the hypothetical data sets. When times from recurrence to death were doubled, the association between treatment effects on DFS and 5-year OS was modest (R(2) = 0.51 for both 2- and 3-year DFS) but remained strong for DFS and 6-year OS (R(2) = 0.67 for both 2- and 3-year DFS) and 7-year OS (R(2) = 0.70 for both 2- and 3-year DFS). The reduced DFS/OS association with extended survival after recurrence was greater in stage II than stage III patients. Multiple simulations provided consistent findings.

CONCLUSION

Extended survival after recurrence reduces the association between treatment effects on 3-year DFS and 5-year OS, particularly in stage II patients; longer follow-up strengthens the association. In modern adjuvant trials, 6 or 7 years may be required to demonstrate OS improvements, further supporting DFS as the preferred primary end point for future adjuvant colon cancer clinical trials.

摘要

目的

我们之前已经验证了无病生存期(DFS)作为氟尿嘧啶辅助结肠癌临床试验中总生存期(OS)的替代指标。新的治疗方法将复发后的生存时间从 1 年延长到了大约 2 年。我们研究了这种改善对 DFS/OS 相关性的可能影响。

方法

分析了 20898 例患者的辅助结肠癌终点(ACCENT)数据集。通过几种算法,对复发患者的复发后死亡时间进行了扩展,评估了中位随访 3 年后 DFS 和不同随访时间(中位随访时间为 5、6 和 7 年)后的 OS 的相关性。

结果

7402 例患者(35%)经历了复发。在假设的数据集中,复发后到死亡的中位时间为 24 个月。当从复发到死亡的时间加倍时,DFS 和 5 年 OS 之间的治疗效果相关性是适度的(2 年和 3 年 DFS 的 R²分别为 0.51),但对于 DFS 和 6 年 OS(2 年和 3 年 DFS 的 R²分别为 0.67)和 7 年 OS(2 年和 3 年 DFS 的 R²分别为 0.70)仍然很强。在复发后生存时间延长的情况下,DFS/OS 相关性的降低在 II 期患者中比 III 期患者更为明显。多项模拟结果一致。

结论

复发后生存时间的延长降低了 3 年 DFS 和 5 年 OS 之间的治疗效果相关性,特别是在 II 期患者中;更长的随访时间加强了这种相关性。在现代辅助试验中,可能需要 6 或 7 年的时间才能证明 OS 的改善,进一步支持将 DFS 作为未来辅助结肠癌临床试验的首选主要终点。

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