Beyond success: unveiling the hidden potential of radiotherapy and immunotherapy in solid tumors.
Yuze WuMing YiMengke NiuBinghan ZhouQi MeiKongming WuPublished in: Cancer communications (London, England) (2024)
Immunotherapy, particularly with immune checkpoint inhibitors, has significantly transformed cancer treatment. Despite its success, many patients struggle to respond adequately or sustain long-lasting clinical improvement. A growing consensus has emerged that radiotherapy (RT) enhances the response rate and overall efficacy of immunotherapy. Although combining RT and immunotherapy has been extensively investigated in preclinical models and has shown promising results, establishing itself as a dynamic and thriving area of research, clinical evidence for this combination strategy over the past five years has shown both positive and disappointing results, suggesting the need for a more nuanced understanding. This review provides a balanced and updated analysis of the combination of immunotherapy and RT. We summarized the preclinical mechanisms through which RT boosts antitumor immune responses and mainly focused on the outcomes of recently updated clinical trials, including those that may not have met expectations. We investigated the optimization of the therapeutic potential of this combined strategy, including key challenges, such as fractionation and scheduling, lymph node irradiation, and toxicity. Finally, we offered insights into the prospects and challenges associated with the clinical translation of this combination therapy, providing a realistic perspective on the current state of research and potential future directions.
Keyphrases
- combination therapy
- lymph node
- clinical trial
- immune response
- end stage renal disease
- early stage
- chronic kidney disease
- ejection fraction
- newly diagnosed
- stem cells
- type diabetes
- multidrug resistant
- radiation induced
- oxidative stress
- squamous cell carcinoma
- prognostic factors
- locally advanced
- metabolic syndrome
- atomic force microscopy
- peritoneal dialysis
- adipose tissue
- mesenchymal stem cells
- patient reported
- double blind