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转移性去势敏感型前列腺癌的管理现状与展望。

Current status and future perspective on the management of metastatic castration-sensitive prostate cancer.

机构信息

Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

Cancer Treat Res Commun. 2022;32:100606. doi: 10.1016/j.ctarc.2022.100606. Epub 2022 Jul 9.

Abstract

Since 1941, the standard treatment for metastatic castration-sensitive prostate cancer (mCSPC) was androgen deprivation therapy (ADT) by surgical or medical castration with or without first-generation antiandrogen. However, the efficacy of ADT does not last in most cases. In the 2010s, de-intensification by intermittent ADT was evaluated by RCTs for mCSPC to mitigate the treatment-emerged burdens. However, intermittent ADT failed to show non-inferiority in OS for mCSPC and is an optional treatment for selected patients with mCSPC. The treatment for patients with mCSPC has improved in the last years. Currently, based on the evidence from RCTs, intensification treatment by adding docetaxel, novel androgen receptor pathway inhibitors and multimodal treatment using radiotherapy to the primary have become new standard treatments for mCSPC. Furthermore, ongoing RCTs have been investigating the clinical values of more intensified treatments by combining multiple effective treatment for mCSPC. In addition, novel treatment using immunotherapeutics such as anti-PD-1 antibody and precision medicine approach using novel imaging and genomic marker has been investigated vigorously. Thus, we review current treatment evidence obtained by RCTs that included patients with mCSPC. The future key to mCSPC treatment could be personalized medicine including translational and clinical medicine aspects, with molecular testing to assess the biological tumor behavior to optimize clinical decision-making.

摘要

自 1941 年以来,转移性去势敏感型前列腺癌(mCSPC)的标准治疗方法是通过手术或医学去势进行雄激素剥夺疗法(ADT),联合或不联合第一代抗雄激素药物。然而,在大多数情况下,ADT 的疗效不会持久。在 21 世纪 10 年代,通过随机对照试验(RCTs)评估了 mCSPC 的间歇性 ADT 去强化治疗,以减轻治疗带来的负担。然而,间歇性 ADT 未能在 OS 方面显示出对 mCSPC 的非劣效性,并且是 mCSPC 特定患者的可选治疗方法。近年来,mCSPC 的治疗方法得到了改善。目前,根据 RCT 的证据,通过在初始治疗中添加多西他赛、新型雄激素受体通路抑制剂和放射治疗的多模式治疗来强化治疗,已经成为 mCSPC 的新的标准治疗方法。此外,正在进行的 RCT 一直在研究通过联合多种有效的 mCSPC 治疗方法来进行更强化治疗的临床价值。此外,还积极研究了使用免疫疗法(如抗 PD-1 抗体)和新型成像及基因组标志物的精准医学方法等新型治疗方法。因此,我们回顾了包括 mCSPC 患者在内的 RCT 获得的当前治疗证据。mCSPC 治疗的未来关键可能是个性化医学,包括转化医学和临床医学方面,通过分子检测评估生物肿瘤行为,以优化临床决策。

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