Genome-wide association studies in advanced prostate cancer: KYUCOG-1401-A study

前列腺癌 全基因组关联研究 单核苷酸多态性 肿瘤科 医学 内科学 血脂异常 雄激素剥夺疗法 遗传关联 癌症 生物信息学 基因型 生物 遗传学 疾病 基因
作者
Masaki Shiota,Shuichi Tatarano,Toshiyuki Kamoto,Hideyasu Matsuyama,Hideki Sakai,Tsukasa Igawa,Tomomi Kamba,Naohiro Fujimoto,Yuya Sekine,Hiroko Kimura,Shintaro Narita,Naoki Terada,Yukihide Momozawa,Shusuke Akamatsu,Tomonori Habuchi,Akira Yokomizo,Seiji Naito,Masatoshi Eto
出处
期刊:Endocrine-related Cancer [Bioscientifica]
卷期号:30 (7) 被引量:5
标识
DOI:10.1530/erc-23-0044
摘要

Androgen-deprivation therapy (ADT) has been widely used for the treatment of advanced prostate cancer. However, prognosis and adverse events (AEs) vary among patients. This study aimed to identify genetic markers able to predict the outcome of ADT. Japanese patients treated with primary ADT for advanced prostate cancer in the KYUCOG-1401 trial were enrolled as a development set. A distinct population of advanced prostate cancer cases treated with ADT was included as a validation set. Single-nucleotide polymorphisms (SNPs) associated with radiographic progression-free survival (rPFS) at 1 year and AEs including de novo diabetes mellitus (DM), arthralgia, and de novo dyslipidemia were identified in the development set by a genome-wide association study (GWAS). The SNPs associated with rPFS in the development study were then genotyped in the validation set. GWAS followed by validation identified SNPs (rs76237622 in PRR27 and rs117573572 in MTAP) that were associated with overall survival (OS) in ADT. A genetic prognostic model using these SNPs showed excellent predictive efficacy for PFS and OS in ADT. In addition, GWAS showed that several SNPs were associated with de novo DM, arthralgia, and de novo dyslipidemia in ADT. This study identified novel multiple SNPs that correlated with outcomes in ADT. Future studies on correlations affecting the therapeutic efficacy of ADT-based combination therapies would make a valuable contribution to the development of personalized medicine.

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