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<p>Metastatic castration-resistant prostate cancer (mCRPC) remains a formidable clinical challenge, with conventional therapies yielding limited efficacy. Immunotherapy combined with radiotherapy (iRT) holds synergistic potential for mCRPC, though mechanistic complexities-including dose-dependent immunomodulation, temporal sequencing dynamics, and tumor microenvironment (TME)-mediated resistance-require further clarification. Radiotherapy enhances tumor immunogenicity by inducing antigen release, improving HLA expression, and activating T cells, thereby potentiating immunotherapy. Clinical trials validate iRT’s efficacy: for example, <sup>177</sup>Lu-PSMA-617 plus standard care prolonged median progression-free survival (PFS) from 3.4 to 8.7&#xa0;months and overall survival (OS) from 11.3 to 15.3&#xa0;months in PSMA+ mCRPC patients. In addition, avelumab combined with stereotactic ablative radiotherapy achieved a median PFS of 8.4&#xa0;months and OS of 14.1&#xa0;months in treatment-refractory mCRPC. Key challenges include optimizing treatment parameters (e.g., dosing, sequencing) and identifying predictive biomarkers. While early results are promising, ongoing research aims to refine iRT protocols and translate mechanistic insights into personalized strategies. This review synthesizes current advances, highlighting synergistic mechanisms, clinical evidence, and unresolved translational hurdles.</p>

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Synergistic potential and challenges of immunotherapy combined with radiotherapy in metastatic castration-resistant prostate cancer: a review of mechanisms and clinical advances

  • 期刊论文

  • 发表日期：

    2025年7月23日

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  • Zengzhao Wei,
  • Xuan Lan,
  • Encun Hou

摘要

Metastatic castration-resistant prostate cancer (mCRPC) remains a formidable clinical challenge, with conventional therapies yielding limited efficacy. Immunotherapy combined with radiotherapy (iRT) holds synergistic potential for mCRPC, though mechanistic complexities-including dose-dependent immunomodulation, temporal sequencing dynamics, and tumor microenvironment (TME)-mediated resistance-require further clarification. Radiotherapy enhances tumor immunogenicity by inducing antigen release, improving HLA expression, and activating T cells, thereby potentiating immunotherapy. Clinical trials validate iRT’s efficacy: for example, 177Lu-PSMA-617 plus standard care prolonged median progression-free survival (PFS) from 3.4 to 8.7 months and overall survival (OS) from 11.3 to 15.3 months in PSMA+ mCRPC patients. In addition, avelumab combined with stereotactic ablative radiotherapy achieved a median PFS of 8.4 months and OS of 14.1 months in treatment-refractory mCRPC. Key challenges include optimizing treatment parameters (e.g., dosing, sequencing) and identifying predictive biomarkers. While early results are promising, ongoing research aims to refine iRT protocols and translate mechanistic insights into personalized strategies. This review synthesizes current advances, highlighting synergistic mechanisms, clinical evidence, and unresolved translational hurdles.