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转移性去势抵抗性前列腺癌的免疫联合治疗——失败试验与未来方向

英文原题:Immunotherapy combinations for metastatic castration-resistant prostate cancer - failed trials and future aspects.

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Immunotherapy combinations for metastatic castration-resistant prostate cancer - failed trials and future aspects.

PubMed 2023/06/30(内容时间) Curr Opin Urol Q2 · IF 2.3(JCR 2025)

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研究思路按摘要原文分段

免疫治疗,目前与免疫检查点阻断同义的一种治疗方式,对前列腺癌来说仍是一个挑战。尽管多项3期试验在联合方案中使用了检查点抑制剂,但迄今为止在总生存期或影像学无进展生存期方面均无获益。然而,针对多种独特细胞表面抗原的新策略正在兴起。这些策略包括独特的疫苗、嵌合抗原受体(CAR)T、双特异性T细胞衔接器平台以及抗体-药物偶联物。

新抗原正被各种免疫策略作为靶点。这些抗原是泛癌种的,因为它们可能在多种癌症上表达,但仍是治疗攻击的有效靶点。总结:单独使用检查点抑制剂或与多种药物如化疗、聚ADP核糖聚合酶(PARP)抑制剂或新型生物制剂联合的免疫治疗,在总生存期(OS)和影像学无进展生存期(rPFS)终点上均遭遇失败。尽管做出了这些努力,仍应继续开展其他免疫学工作,以开发独特的肿瘤靶向策略。

展开英文摘要原文

PURPOSE OF REVIEW: Immunotherapy, a treatment modality currently synonymous with immune checkpoint blockade remains a challenge for prostate cancer. Despite multiple phase 3 trials using checkpoint inhibitors in combinatorial approaches, there have been no benefits to date in overall survival or radiographic progression free survival.

However, newer strategies prevail that are directed to a variety of unique cell surface antigens. These strategies include unique vaccines, chimeric antigen receptor (CAR) T, bispecific T cell engager platforms, and antibody-drug conjugates. RECENT FINDINGS: New antigens are being targeted by various immunologic strategies. These antigens are pan-carcinoma as they may be expressed on a variety of cancers but remains effective targets for therapeutic attack.

SUMMARY: Immunotherapy with checkpoint inhibitors alone or in combination with a variety of agents such as chemotherapy, poly-ADP ribose polymerase (PARP) inhibitors or novel biologics have met with failure in the endpoints of overall survival (OS) and radiographic progresson-free survival (rPFS). Despite these efforts, other immunologic efforts to develop unique tumor-targeted strategies should be continued.

论文信息

作者
Slovin SF
单位
Memorial Sloan-Kettering Cancer Center, New York, New York, USA.United States
文献类型
综述
期刊
Current opinion in urology2023 Sep 1
原文标识
PubMed 37395505 · DOI 10.1097/MOU.0000000000001115