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帕博利珠单抗在微卫星高度不稳定(MSI-high)和乳腺癌易感基因(BRCA)阳性的去势抵抗性前列腺癌中的疗效。

Efficacy of pembrolizumab in MSI-high and BRCA-positive castration-resistant prostate cancer.

作者信息

Higa Keita, Yamamoto Satoshi, Kurokawa Koichiro, Watanabe Koki, Bamba Hiroki, Kanaoka Sanji, Nakamura Kazuyoshi

机构信息

Department of Urology, Kimitsu Chuo Byoin, Japan.

Department of Urology, Kimitsu Chuo Byoin, Japan.

出版信息

Cancer Genet. 2025 Sep;296-297:41-44. doi: 10.1016/j.cancergen.2025.06.002. Epub 2025 Jun 10.

DOI:10.1016/j.cancergen.2025.06.002
PMID:40527113
Abstract

This report presents a rare case of metastatic castration-resistant prostate cancer (CRPC) in an adult patient characterized by dual molecular alterations: microsatellite instability-high (MSI-H) and a BRCA2 mutation. Despite initial treatment with castration, Abiraterone, and sequential chemotherapy with docetaxel and cabazitaxel, the patient progressed to CRPC. Genetic testing revealed MSI-H and a BRCA2 mutation, prompting pembrolizumab therapy. The treatment led to a dramatic prostate-specific antigen (PSA) reduction . This case underscores the importance of comprehensive genomic profiling for advanced prostate cancer. MSI-H tumors often respond to immune checkpoint inhibitors (ICIs) such as pembrolizumab, while BRCA2 mutations are associated with poly(ADP-ribose) polymerase inhibitors (PARPi) sensitivity. This dual alteration presents therapeutic challenges, as evidenced by pembrolizumab's remarkable efficacy in this patient, highlighting its potential as a treatment option for MSI-H and BRCA-positive CRPC. Moreover, next-generation sequencing (NGS) played a crucial role in identifying actionable biomarkers not detected by earlier BRCA analyses, emphasizing the necessity of thorough genetic testing. Further research is needed to optimize treatment strategies for cases with coexisting MSI-H and BRCA mutations, including exploring the synergistic effects of ICIs and PARP i. This case demonstrates the promise of pembrolizumab and advances the understanding of genetic testing's role in tailoring therapies for complex molecular profiles in prostate cancer.

摘要

本报告介绍了一例成年转移性去势抵抗性前列腺癌(CRPC)罕见病例,其特征为双分子改变:微卫星高度不稳定(MSI-H)和BRCA2突变。尽管最初接受了去势治疗、阿比特龙治疗,以及多西他赛和卡巴他赛序贯化疗,但患者仍进展为CRPC。基因检测显示为MSI-H和BRCA2突变,于是开始使用帕博利珠单抗治疗。该治疗导致前列腺特异性抗原(PSA)显著降低。此病例强调了晚期前列腺癌综合基因组分析的重要性。MSI-H肿瘤通常对免疫检查点抑制剂(ICI)如帕博利珠单抗有反应,而BRCA2突变与聚(ADP-核糖)聚合酶抑制剂(PARPi)敏感性相关。这种双重改变带来了治疗挑战,帕博利珠单抗在该患者中显著的疗效证明了这一点,突出了其作为MSI-H和BRCA阳性CRPC治疗选择的潜力。此外,下一代测序(NGS)在识别早期BRCA分析未检测到的可操作生物标志物方面发挥了关键作用,强调了全面基因检测的必要性。需要进一步研究以优化MSI-H和BRCA突变共存病例的治疗策略,包括探索ICI和PARPi的协同作用。该病例展示了帕博利珠单抗的前景,并推动了对基因检测在为前列腺癌复杂分子谱定制治疗中作用的理解。

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