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多西他赛联合奥沙利铂和 S-1(DOS)与奥沙利铂联合 S-1(SOX)用于治疗局部晚期胃或胃食管结合部腺癌(MATCH)的围手术期化疗:一项开放标签、随机、2 期临床试验。

Perioperative chemotherapy with docetaxel plus oxaliplatin and S-1 (DOS) versus oxaliplatin plus S-1 (SOX) for the treatment of locally advanced gastric or gastro-esophageal junction adenocarcinoma (MATCH): an open-label, randomized, phase 2 clinical trial.

机构信息

Department of Medical Oncology, National Cancer Center/ National Clinical Research Center for Cancer/ Cancer Hospital, Chinese Academy of Medical Sciences, and Peking Union Medical College, No. 17, Panjiayuannanli Street, Chaoyang District, Beijing, 100021, China.

Department of Pancreatic and Gastric Surgery, National Cancer Center/ National Clinical Research Center for Cancer/ Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.

出版信息

Gastric Cancer. 2024 May;27(3):571-579. doi: 10.1007/s10120-024-01471-z. Epub 2024 Mar 8.

DOI:10.1007/s10120-024-01471-z
PMID:38457083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11016518/
Abstract

BACKGROUND

It remains unclear whether addition of docetaxel to the combination of a platinum and fluoropyrimidine could provide more clinical benefits than doublet chemotherapies in the perioperative treatment for locally advanced gastric/gastro-esophageal junction (LAG/GEJ) cancer in Asia. In this randomized, phase 2 study, we assessed the efficacy and safety of perioperative docetaxel plus oxaliplatin and S-1 (DOS) versus oxaliplatin plus S-1 (SOX) in LAG/GEJ adenocarcinoma patients.

METHODS

Patients with cT3-4 N M0 G/GEJ adenocarcinoma were randomized (1:1) to receive 4 cycles of preoperative DOS or SOX followed by D2 gastrectomy and another 4 cycles of postoperative chemotherapy. The primary endpoint was major pathological response (MPR).

RESULTS

From Aug, 2015 to Dec, 2019,154 patients were enrolled and 147 patients included in final analysis, with a median age of 60 (26-73) years. DOS resulted in significantly higher MPR (25.4 vs. 11.8%, P = 0.04). R0 resection rate, the 3-year PFS and 3-year OS rates were 78.9 vs. 61.8% (P = 0.02), 52.3 vs. 35% (HR 0.667, 95% CI: 0.432-1.029, Log rank P = 0.07) and 57.5 vs. 49.2% (HR 0.685, 95% CI: 0.429-1.095, Log rank P = 0.11) in the DOS and SOX groups, respectively. Patients who acquired MPR experienced significantly better survival. DOS had similar tolerance to SOX.

CONCLUSIONS

Perioperative DOS improved MPR significantly and tended to produce longer PFS compared to SOX in LAG/GEJ cancer in Asia, and might be considered as a preferred option for perioperative chemotherapy and worth further investigation.

摘要

背景

局部晚期胃/胃食管交界(LAG/GEJ)腺癌患者在亚洲的围手术期治疗中,多西紫杉醇联合铂类和氟嘧啶类药物的疗效是否优于双药化疗仍不清楚。在这项随机、2 期研究中,我们评估了围手术期多西紫杉醇联合奥沙利铂和 S-1(DOS)与奥沙利铂联合 S-1(SOX)在 LAG/GEJ 腺癌患者中的疗效和安全性。

方法

cT3-4 N M0 G/GEJ 腺癌患者按 1:1 随机分为 4 个周期的术前 DOS 或 SOX 治疗,随后行 D2 胃切除术,再进行 4 个周期的术后化疗。主要终点为主要病理缓解(MPR)。

结果

2015 年 8 月至 2019 年 12 月,共纳入 154 例患者,最终分析纳入 147 例患者,中位年龄为 60(26-73)岁。DOS 组 MPR 显著更高(25.4% vs. 11.8%,P=0.04)。R0 切除率、3 年 PFS 和 3 年 OS 率分别为 78.9% vs. 61.8%(P=0.02)、52.3% vs. 35%(HR 0.667,95%CI:0.432-1.029,对数秩 P=0.07)和 57.5% vs. 49.2%(HR 0.685,95%CI:0.429-1.095,对数秩 P=0.11)。获得 MPR 的患者生存情况明显改善。DOS 的耐受性与 SOX 相似。

结论

与 SOX 相比,围手术期 DOS 可显著提高 MPR,且倾向于提高 LAG/GEJ 癌症患者的 PFS,可作为围手术期化疗的首选方案,值得进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/11016518/b96228dfebf8/10120_2024_1471_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/11016518/44eb7e75dac6/10120_2024_1471_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/11016518/b96228dfebf8/10120_2024_1471_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/11016518/44eb7e75dac6/10120_2024_1471_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2f4/11016518/b96228dfebf8/10120_2024_1471_Fig2_HTML.jpg

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