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III 期结肠癌患者辅助化疗持续时间的影响(IDEA 协作组):来自六项随机、III 期临床试验的前瞻性、汇总分析的最终结果。

Effect of duration of adjuvant chemotherapy for patients with stage III colon cancer (IDEA collaboration): final results from a prospective, pooled analysis of six randomised, phase 3 trials.

机构信息

Sorbonne Université and Hôpital Saint Antoine, Paris, France.

Dana-Farber Cancer Institute, Boston, MA, USA.

出版信息

Lancet Oncol. 2020 Dec;21(12):1620-1629. doi: 10.1016/S1470-2045(20)30527-1.

Abstract

BACKGROUND

A prospective, pooled analysis of six randomised phase 3 trials was done to investigate disease-free survival regarding non-inferiority of 3 months versus 6 months of adjuvant chemotherapy for patients with stage III colon cancer; non-inferiority was not shown. Here, we report the final overall survival results.

METHODS

In this prospective, pooled analysis of six randomised phase 3 trials, we included patients with stage III colon cancer aged at least 18 years with an Eastern Cooperative Oncology Group performance status of 0-1 recruited between June 20, 2007, and Dec 31, 2015, across 12 countries in the CALGB/SWOG 80702, IDEA France, SCOT, ACHIEVE, TOSCA, and HORG trials, who started any treatment (modified intention-to-treat). Patients in all trials were randomly assigned to 3 months or 6 months of adjuvant fluorouracil, leucovorin, and oxaliplatin (FOLFOX) every 2 weeks or capecitabine and oxaliplatin (CAPOX) in different doses and methods every 3 weeks, at the treating physician's discretion. The primary endpoint was disease-free survival (time to relapse, secondary colorectal primary tumour, or death due to all causes), and overall survival (time to death due to all causes) was the prespecified secondary endpoint. The non-inferiority margin for overall survival was set as a hazard ratio (HR) of 1·11. Pre-planned subgroup analyses included regimen and risk group. Non-inferiority was declared if the one-sided false discovery rate adjusted (FDRadj) p value was less than 0·025.

FINDINGS

With median follow-up of 72·3 months (IQR 72·2-72·5), 2584 deaths among 12 835 patients were observed. 5064 (39·5%) patients received CAPOX and 7771 (60·5%) received FOLFOX. 5-year overall survival was 82·4% (95% CI 81·4-83·3) with 3 months of therapy and 82·8% (81·8-83·8) with 6 months of therapy (HR 1·02 [95% CI 0·95-1·11]; non-inferiority FDRadj p=0·058). For patients treated with CAPOX, 5-year overall survival was 82·1% (80·5-83·6) versus 81·2% (79·2-82·9; HR 0·96 [0·85-1·08]); non-inferiority FDRadj p=0·033), and for patients treated with FOLFOX 5-year overall survival was 82·6% (81·3-83·8) and 83·8% (82·6-85·0; HR 1·07 [0·97-1·18]; non-inferiority FDRadj p=0·34). Updated disease-free survival results confirmed previous findings (HR 1·08 [95% CI 1·02-1·15]; non-inferiority FDRadj p=0·25). Data on adverse events were not further recorded.

INTERPRETATION

Non-inferiority of 3 months versus 6 months of adjuvant chemotherapy for patients with stage III colon cancer was not confirmed in terms of overall survival, but the absolute 0·4% difference in 5-year overall survival should be placed in clinical context. Overall survival results support the use of 3 months of adjuvant CAPOX for most patients with stage III colon cancer. This conclusion is strengthened by the substantial reduction of toxicities, inconveniencies, and cost associated with a shorter treatment duration.

FUNDING

US National Cancer Institute.

摘要

背景

一项针对六项随机 3 期临床试验的前瞻性汇总分析旨在调查 III 期结肠癌患者辅助化疗 3 个月与 6 个月的无病生存率是否存在非劣效性;结果显示无病生存率非劣效性不成立。在此,我们报告最终的总生存结果。

方法

在这项针对六项随机 3 期临床试验的前瞻性汇总分析中,我们纳入了年龄至少 18 岁、东部肿瘤协作组体力状态为 0-1 分、于 2007 年 6 月 20 日至 2015 年 12 月 31 日在 12 个国家/地区招募的 III 期结肠癌患者,这些患者参与了 CALGB/SWOG 80702、IDEA France、SCOT、ACHIEVE、TOSCA 和 HORG 试验,他们接受了任何治疗(改良意向治疗)。所有试验中的患者均随机分配至接受每 2 周一次的氟尿嘧啶、亚叶酸钙和奥沙利铂(FOLFOX)3 个月或每 3 周一次的卡培他滨和奥沙利铂(CAPOX)不同剂量和方法的辅助治疗,具体方案由治疗医生决定。主要终点为无病生存率(复发、继发性结直肠原发肿瘤或任何原因导致的死亡时间),总生存(任何原因导致的死亡时间)是预设的次要终点。总生存的非劣效性边界设定为风险比(HR)为 1.11。预先计划的亚组分析包括方案和风险组。如果单侧假发现率调整(FDRadj)p 值小于 0.025,则宣布非劣效性。

结果

中位随访 72.3 个月(IQR 72.2-72.5),在 12835 例患者中观察到 2584 例死亡。5064 例(39.5%)患者接受 CAPOX 治疗,7771 例(60.5%)患者接受 FOLFOX 治疗。3 个月治疗组的 5 年总生存率为 82.4%(95%CI 81.4-83.3),6 个月治疗组为 82.8%(81.8-83.8)(HR 1.02 [95%CI 0.95-1.11];非劣效性 FDRadj p=0.058)。接受 CAPOX 治疗的患者中,5 年总生存率为 82.1%(80.5-83.6)与 81.2%(79.2-82.9)(HR 0.96 [0.85-1.08]);非劣效性 FDRadj p=0.033),接受 FOLFOX 治疗的患者中,5 年总生存率为 82.6%(81.3-83.8)和 83.8%(82.6-85.0)(HR 1.07 [0.97-1.18];非劣效性 FDRadj p=0.34)。更新的无病生存率结果证实了先前的发现(HR 1.08 [95%CI 1.02-1.15];非劣效性 FDRadj p=0.25)。未进一步记录关于不良事件的数据。

解释

III 期结肠癌患者辅助化疗 3 个月与 6 个月的无病生存率非劣效性未得到确认,但 5 年总生存率的绝对差异为 0.4%,应置于临床背景下考虑。总生存结果支持大多数 III 期结肠癌患者使用 3 个月的辅助 CAPOX。这一结论得到了与较短治疗持续时间相关的毒性、不便和成本的大量减少的支持。

资金来源

美国国立癌症研究所。

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