Comprehensive Genomic Profiling Testing for Castration-Resistant Prostate Cancer in Advanced Elderly Patients: A Single-Center Retrospective Cohort Study.

IF 2.5 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Prostate Pub Date : 2025-09-01 Epub Date: 2025-06-10 DOI:10.1002/pros.24926
Takafumi Fukushima, Keisuke Goto, Yoshinori Nakano, Shinsaku Tasaka, Kyohsuke Iwane, Ryo Tasaka, Kohei Kobatake, Akihiro Goriki, Asuka Toshida, Akiko Abe, Misako Ishihara, Hikaru Nakahara, Masanori Motonaga, Kentaro Tokumo, Yasutoshi Fujii, Hayes Clair Nelson, Hiroaki Niitsu, Shinya Ohara, Yuji Urabe, Wataru Okamoto, Eiso Hiyama, Koji Arihiro, Takao Hinoi, Nobuyuki Hinata
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引用次数: 0

Abstract

Background: Prostate cancer (PCa) is the second most common solid tumor in men, and its incidence is strongly dependent on age. With the aging global population, this poses a significant medical and sociodemographic issue. As treatment options for castration-resistant prostate cancer (CRPC) expand, the proportion of elderly patients with CRPC is expected to increase. Comprehensive genomic profiling (CGP) testing is becoming increasingly utilized for PCa; however, evidence on age-related outcomes or benefits is limited. This study aimed to evaluate the efficacy of CGP testing in advanced elderly patients with CRPC compared to younger patients.

Methods: We conducted a single-center, retrospective cohort study at Hiroshima University, including Japanese men aged ≥ 20 years who underwent CGP testing for CRPC between January 1, 2021, and May 31, 2024. Patients were categorized into the following two groups: the "advanced elderly group" (≥ 75 years) and the "younger group" (< 75 years). Clinical data were retrospectively extracted from medical records. CGP testing was performed using the FoundationOne® CDx, FoundationOne® Liquid CDx, Gurdant360® CDx, PleSSision Exome, or OncoGuide™ NCC Oncopanel System. Pathogenic alterations were categorized into relevant subgroups. Statistical analyzes were performed to compare patient backgrounds, genomic subgroups, and outcomes between the age groups.

Results: Overall, 85 patients (median age: 74 years) were included in the analysis, with 38 and 47 in the advanced elderly and younger groups, respectively. No significant differences were observed in baseline clinical characteristics other than age. CGP testing identified 355 pathogenic variants (140 and 215 in the advanced elderly and younger groups, respectively), with similar distributions of alteration types across the two groups. Among the subgroups, DNA repair and homologous recombination repair-related gene alterations were significantly more frequent in the younger group (p = 0.017) than in the advanced elderly group. Overall survival (OS) did not differ significantly between the age groups. However, patients who received systemic chemotherapy based on CGP testing results had significantly better OS than those who did not receive systemic therapy (p = 0.045). This trend remained significant in the advanced elderly group (p = 0.006).

Conclusions: CGP testing appears to offer clinical benefits for patients with CRPC, regardless of age.

晚期老年患者去势抵抗性前列腺癌的综合基因组谱检测:一项单中心回顾性队列研究。
背景:前列腺癌(PCa)是男性第二大常见的实体肿瘤,其发病率与年龄密切相关。随着全球人口老龄化,这构成了一个重大的医学和社会人口问题。随着去势抵抗性前列腺癌(CRPC)治疗方案的扩大,老年CRPC患者的比例预计会增加。综合基因组分析(CGP)测试越来越多地用于PCa;然而,与年龄相关的结果或益处的证据有限。本研究旨在评估CGP检测在晚期老年CRPC患者中的疗效,并与年轻患者进行比较。方法:我们在广岛大学进行了一项单中心、回顾性队列研究,纳入了年龄≥20岁的日本男性,他们在2021年1月1日至2024年5月31日期间接受了CRPC的CGP检测。患者分为两组:“高龄组”(≥75岁)和“年轻组”(结果:总体纳入85例患者(中位年龄:74岁),高龄组38例,年轻组47例。除年龄外,基线临床特征无显著差异。CGP检测鉴定出355种致病变异(老年晚期和年轻组分别为140种和215种),两组的变异类型分布相似。在亚组中,年轻组的DNA修复和同源重组修复相关基因改变明显高于高龄组(p = 0.017)。总生存率(OS)在年龄组间无显著差异。然而,基于CGP检测结果接受全身化疗的患者的OS明显优于未接受全身治疗的患者(p = 0.045)。这一趋势在高龄组中仍然显著(p = 0.006)。结论:无论年龄大小,CGP检测似乎都能为CRPC患者提供临床益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Prostate
Prostate 医学-泌尿学与肾脏学
CiteScore
5.10
自引率
3.60%
发文量
180
审稿时长
1.5 months
期刊介绍: The Prostate is a peer-reviewed journal dedicated to original studies of this organ and the male accessory glands. It serves as an international medium for these studies, presenting comprehensive coverage of clinical, anatomic, embryologic, physiologic, endocrinologic, and biochemical studies.
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