Genome-wide DNA methylation status is a predictor of the efficacy of anti-EGFR antibodies in the second-line treatment of metastatic colorectal cancer: Translational research of the EPIC trial.

IF 2.5 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY International Journal of Colorectal Disease Pub Date : 2024-06-11 DOI:10.1007/s00384-024-04659-y
Kota Ouchi, Shin Takahashi, Keiju Sasaki, Yuya Yoshida, Sakura Taniguchi, Yuki Kasahara, Keigo Komine, Hiroo Imai, Ken Saijo, Hidekazu Shirota, Masanobu Takahashi, Chikashi Ishioka
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Abstract

Purpose: The genome-wide DNA methylation status (GWMS) predicts of therapeutic response to anti-epidermal growth factor receptor (EGFR) antibodies in treating metastatic colorectal cancer. We verified the significance of GWMS as a predictive factor for the efficacy of anti-EGFR antibodies in the second-line treatment of metastatic colorectal cancer.

Methods: Clinical data were obtained from a prospective trial database, and a genome-wide DNA methylation analysis was performed. GWMS was classified into high-methylated colorectal cancer (HMCC) and low-methylated colorectal cancer (LMCC). The patients were divided into subgroups according to the treatment arm (cetuximab plus irinotecan or irinotecan alone) and GWMS, and the clinical outcomes were compared between the subgroups.

Results: Of the 112 patients, 58 (51.8%) were in the cetuximab plus irinotecan arm, and 54 (48.2%) were in the irinotecan arm; 47 (42.0%) were in the HMCC, and 65 (58.0%) were in the LMCC group regarding GWMS. Compared with the LMCC group, the progression-free survival (PFS) was significantly shortened in the HMCC group in the cetuximab plus irinotecan arm (median 1.4 vs. 4.1 months, p = 0.001, hazard ratio = 2.56), whereas no significant differences were observed in the irinotecan arm. A multivariate analysis showed that GWMS was an independent predictor of PFS and overall survival (OS) in the cetuximab plus irinotecan arm (p = 0.002, p = 0.005, respectively), whereas GWMS did not contribute to either PFS or OS in the irinotecan arm.

Conclusions: GWMS was a predictive factor for the efficacy of anti-EGFR antibodies in the second-line treatment of metastatic colorectal cancer.

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全基因组 DNA 甲基化状态是抗表皮生长因子受体(EGFR)抗体二线治疗转移性结直肠癌疗效的预测因子:EPIC试验的转化研究。
目的:全基因组DNA甲基化状态(GWMS)可预测抗表皮生长因子受体(EGFR)抗体治疗转移性结直肠癌的疗效。我们验证了 GWMS 作为抗表皮生长因子受体(EGFR)抗体二线治疗转移性结直肠癌疗效预测因素的重要性:方法:从前瞻性试验数据库中获取临床数据,并进行全基因组DNA甲基化分析。GWMS分为高甲基化结直肠癌(HMCC)和低甲基化结直肠癌(LMCC)。根据治疗方法(西妥昔单抗联合伊立替康或单用伊立替康)和GWMS将患者分为亚组,并比较亚组之间的临床结果:在112例患者中,西妥昔单抗联合伊立替康组58例(51.8%),伊立替康组54例(48.2%);在GWMS方面,HMCC组47例(42.0%),LMCC组65例(58.0%)。与LMCC组相比,西妥昔单抗联合伊立替康组的HMCC组无进展生存期(PFS)明显缩短(中位1.4个月对4.1个月,P=0.001,危险比=2.56),而伊立替康组无明显差异。多变量分析显示,在西妥昔单抗加伊立替康治疗组中,GWMS是PFS和总生存期(OS)的独立预测因素(分别为p = 0.002和p = 0.005),而在伊立替康治疗组中,GWMS对PFS和OS均无影响:结论:GWMS是抗EGFR抗体二线治疗转移性结直肠癌疗效的预测因素。
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来源期刊
CiteScore
4.90
自引率
3.60%
发文量
206
审稿时长
3-8 weeks
期刊介绍: The International Journal of Colorectal Disease, Clinical and Molecular Gastroenterology and Surgery aims to publish novel and state-of-the-art papers which deal with the physiology and pathophysiology of diseases involving the entire gastrointestinal tract. In addition to original research articles, the following categories will be included: reviews (usually commissioned but may also be submitted), case reports, letters to the editor, and protocols on clinical studies. The journal offers its readers an interdisciplinary forum for clinical science and molecular research related to gastrointestinal disease.
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