前列腺癌的新靶向疗法:从放射性配体疗法到 PARP 抑制剂和免疫疗法。

IF 1.5 4区 医学
Francesco Ceci, Lighea S Airò Farulla, Elena Bonatto, Laura Evangelista, Marta Aliprandi, Luigi G Cecchi, Francesco Mattana, Alessandro Bertocchi, Fabio DE Vincenzo, Matteo Perrino, Nadia Cordua, Federica Borea, Paolo A Zucali
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引用次数: 0

摘要

前列腺癌(PCa)仍然是全球健康面临的重大挑战,尤其是在晚期。尽管在早期检测和治疗方面取得了进展,但前列腺癌仍是男性第二大常见癌症。本综述旨在概述当前治疗 PCa 的方法和创新,重点关注最新进展和持续面临的挑战。我们对临床试验和研究进行了叙述性综述,重点关注 PARP 抑制剂(PARPis)、磷酸肌酸 3 激酶-蛋白激酶 B 抑制剂、免疫疗法和放射性配体疗法(RLTs)。数据来源于主要的临床试验数据库和同行评审期刊。雄激素剥夺疗法和雄激素受体通路抑制剂仍是治疗阉割敏感型和早期阉割耐药 PCa (CRPC) 的基础疗法。奥拉帕利(olaparib)和鲁卡帕利(rucaparib)等 PARPi 类药物已成为治疗同源重组修复基因突变的转移性 CRPC 的重要药物,凸显了个性化医疗的重要性。免疫检查点抑制剂(ICIs)的临床疗效仅限于特定的 PCa 亚组,在微卫星不稳定性/错配修复或细胞周期蛋白依赖性激酶 12 基因改变的患者中疗效显著改善,这凸显了将当前研究的重点放在识别和描述这些亚组以最大限度发挥 ICIs 临床疗效的重要性。RLT已显示出治疗mCRPC的有效性。不同的α发射体(如[225Ac]PSMA)和β发射体化合物(如[177Lu]PSMA)因其能量转移特性而对治疗产生不同的影响。VISION和TheraP等临床试验表明,RLT(尤其是[177Lu]PSMA-617)具有积极的疗效,因此获得了FDA的批准。目前正在进行的试验和未来展望探索了[225Ac]PSMA的潜力,旨在改善mCRPC患者的治疗效果。PCa 的治疗形势不断变化,既有疗法和新型疗法都取得了重大进展。在基因和分子研究的指导下,激素疗法、化疗、PARPis、免疫疗法和RLT的结合为个性化治疗开辟了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New target therapies in prostate cancer: from radioligand therapy, to PARP-inhibitors and immunotherapy.

Prostate cancer (PCa) remains a significant global health challenge, particularly in its advanced stages. Despite progress in early detection and treatment, PCa is the second most common cancer diagnosis among men. This review aims to provide an overview of current therapeutic approaches and innovations in PCa management, focusing on the latest advancements and ongoing challenges. We conducted a narrative review of clinical trials and research studies, focusing on PARP inhibitors (PARPis), phosphoinositide 3 kinase-protein kinase B inhibitors, immunotherapy, and radioligand therapies (RLTs). Data was sourced from major clinical trial databases and peer-reviewed journals. Androgen deprivation therapy and androgen-receptor pathway inhibitors remain foundational in managing castration-sensitive and early-stage castration-resistant PCa (CRPC). PARPi's, such as olaparib and rucaparib, have emerged as vital treatments for metastatic CRPC with homologous recombination repair gene mutations, highlighting the importance of personalized medicine. Immune checkpoint inhibitors (ICIs) have shown clinical benefit limited to specific subgroups of PCa, demonstrating significant improvement in efficacy in patients with microsatellite instability/mismatch repair or cyclin-dependent kinase 12 alteration, highlighting the importance of focusing ongoing research on identifying and characterizing these subgroups to maximize the clinical benefits of ICIs. RLTs have shown effectiveness in treating mCRPC. Different alpha emitters (like [225Ac]PSMA) and beta emitters compounds (like [177Lu]PSMA) impact treatment differently due to their energy transfer characteristics. Clinical trials like VISION and TheraP have demonstrated positive outcomes with RLT, particularly [177Lu]PSMA-617, leading to FDA approval. Ongoing trials and future perspectives explore the potential of [225Ac]PSMA, aiming to improve outcomes for patients with mCRPC. The landscape of PCa treatment is evolving, with significant advancements in both established and novel therapies. The combination of hormonal therapies, chemotherapy, PARPis, immunotherapy, and RLTs, guided by genetic and molecular insights, opens new possibilities for personalized treatment.

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来源期刊
the Quarterly Journal of Nuclear Medicine and Molecular Imaging
the Quarterly Journal of Nuclear Medicine and Molecular Imaging Medicine-Radiology, Nuclear Medicine and Imaging
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84
期刊介绍: The Quarterly Journal of Nuclear Medicine and Molecular Imaging publishes scientific papers on clinical and experimental topics of nuclear medicine. Manuscripts may be submitted in the form of editorials, original articles, review articles and special articles. The journal aims to provide its readers with papers of the highest quality and impact through a process of careful peer review and editorial work.
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