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III 期随机临床试验比较卡培他滨 6 个月与 12 个月作为 III 期结肠癌辅助化疗:JFMC37-0801 研究的最终结果。

Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study.

机构信息

Department of Surgery, Division of Lower Gastrointestinal Surgery, Hyogo College of Medicine, Hyogo, Japan.

Department of Surgery, Gifu Prefectural General Medical Center, Gifu, Japan.

出版信息

Br J Cancer. 2019 Apr;120(7):689-696. doi: 10.1038/s41416-019-0410-0. Epub 2019 Mar 5.

DOI:10.1038/s41416-019-0410-0
PMID:30833647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6461756/
Abstract

BACKGROUND

Up to 6-months oxaliplatin-containing regimen is now widely accepted as a standard adjuvant chemotherapy for stage III colorectal cancer (CRC). However, oral fluoropyrimidine monotherapy is used for some part of patients, especially in Asian countries including Japan, and its optimal duration is yet to be fully investigated.

METHODS

A total of 1306 patients with curatively-resected stage III CRC were randomly assigned to receive capecitabine (2500 mg/m/day) for 14 out of 21 days for 6 (n = 654) or 12 (n = 650) months. The primary endpoint was disease-free survival (DFS), and the secondary endpoints were relapse-free survival (RFS), overall survival (OS), and adverse events.

RESULTS

The 3- and 5-year DFS were 70.0% and 65.3% in the 6M group and 75.3% and 68.7% in the 12M group, respectively (p = 0.0549, HR = 0.858, 90% CI: 0.732-1.004). The 5-year RFS was 69.3% and 74.1% in the 6M and 12M groups, respectively (p = 0.0143, HR = 0.796, 90% CI: 0.670-0.945). The 5-year OS was 83.2% and 87.6%, respectively (p = 0.0124, HR = 0.727, 90% CI: 0.575-0.919). The incidence of overall grade 3-4 adverse events was almost comparable in both groups.

CONCLUSIONS

Although 12-month adjuvant capecitabine did not demonstrate superior DFS to that of 6-month, the observed better RFS and OS in the 12-month treatment period could be of value in selected cases.

摘要

背景

目前,含奥沙利铂的 6 个月治疗方案已被广泛接受为 III 期结直肠癌(CRC)的标准辅助化疗。然而,在包括日本在内的亚洲国家,部分患者仍使用口服氟嘧啶单药治疗,其最佳持续时间尚未得到充分研究。

方法

共 1306 例可治愈性切除的 III 期 CRC 患者被随机分配接受卡培他滨(2500mg/m/天)治疗,21 天为 1 个周期,6 个月(n=654)或 12 个月(n=650)。主要终点为无病生存(DFS),次要终点为无复发生存(RFS)、总生存(OS)和不良事件。

结果

6 个月组和 12 个月组的 3 年和 5 年 DFS 分别为 70.0%和 65.3%,75.3%和 68.7%(p=0.0549,HR=0.858,90%CI:0.732-1.004)。6 个月组和 12 个月组的 5 年 RFS 分别为 69.3%和 74.1%(p=0.0143,HR=0.796,90%CI:0.670-0.945)。5 年 OS 分别为 83.2%和 87.6%(p=0.0124,HR=0.727,90%CI:0.575-0.919)。两组总体 3-4 级不良事件发生率几乎相当。

结论

尽管 12 个月辅助卡培他滨治疗并未显示出优于 6 个月的 DFS,但在 12 个月治疗期间观察到的更好的 RFS 和 OS 可能对某些病例具有价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/e96a72d9fa6c/41416_2019_410_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/ccf293beea81/41416_2019_410_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/a505d8cc918a/41416_2019_410_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/3df47871d17e/41416_2019_410_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/e96a72d9fa6c/41416_2019_410_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/ccf293beea81/41416_2019_410_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/a505d8cc918a/41416_2019_410_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/3df47871d17e/41416_2019_410_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840b/6461756/e96a72d9fa6c/41416_2019_410_Fig4_HTML.jpg

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