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Immune checkpoint inhibitor nivolumab induces durable response in microsatellite instability-high and DNA damage repair-deficient metastatic castration-resistant prostate cancer

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机构: [1]Department of Urology and Institute of Urology, West China Hospital, Sichuan University, Chengdu, China. [2]Department of Urology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.
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Prostate cancer is the second most common malignancy in men worldwide, and its incidence in China continues to rise [1]. Despite advances in androgen deprivation therapy (ADT) and androgen receptor (AR) pathway inhibitors, many patients eventually progress to metastatic castration-resistant prostate cancer (mCRPC). Based on molecular features, mCRPC can be classified into AR-driven, DNA damage repair (DDR)-deficient, microsatellite instability-high (MSIH)/mismatch repair-deficient (dMMR), and neuroendocrinelike subtypes, each with distinct biological characteristics and therapeutic implications [2]. Although DDR and MMR deficiencies are relatively uncommon, they offer actionable therapeutic opportunities. MSI-H/dMMR tumours are associated with a high tumour mutational burden (TMB) and abundant neoantigen expression, providing a strong rationale for immune checkpoint blockade. MSI-H/dMMR status has been used to guide programmed death 1 (PD-1) inhibitor therapy in various malignancies, e.g., in colorectal cancer, providing a rationale for its application in selected patients with mCRPC [3].

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大类 | 2 区 医学
小类 | 2 区 泌尿学与肾脏学
最新[2025]版:
大类 | 2 区 医学
小类 | 2 区 泌尿学与肾脏学
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第一作者机构: [1]Department of Urology and Institute of Urology, West China Hospital, Sichuan University, Chengdu, China.
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