4.7 Review

Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment

Journal

CLINICAL CANCER RESEARCH
Volume 28, Issue 17, Pages 3652-3657

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-21-4332

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Funding

  1. Dutch Cancer Society [12567]
  2. Dutch Research Council (NWO) [09150172010054]

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The development of immunotherapy, particularly immune checkpoint inhibitors (ICI), has revolutionized cancer treatment, but its efficacy is still limited. Radiotherapy has great potential as an effective treatment combination strategy, by inducing immunogenic cell death and sensitizing tumors to ICI. Targeted radionuclide therapy (TRT) is a promising approach that delivers therapeutic radiation dose specifically to tumor cells, with ongoing clinical trials to assess its safety and efficacy in combination with ICI. Combining TRT and ICI may improve therapeutic response in patients with cancer, but further research is needed to determine optimal conditions for maximum efficacy.
The development of immunotherapy, in particular immune checkpoint inhibitors (ICI), has revolutionized cancer treatment in the past decades. However, its efficacy is still limited to subgroups of patients with cancer. Therefore, effective treatment combination strategies are needed. Here, radiotherapy is highly promising, as it can induce immunogenic cell death, triggering the release of pro-inflammatory cytokines, thereby creating an immunogenic pheno-type and sensitizing tumors to ICI. Recently, targeted radionuclide therapy (TRT) has attained significant interest for cancer treatment. In this approach, a tumor-targeting radiopharmaceutical is used to specifically deliver a therapeutic radiation dose to all tumor cells, including distant metastatic lesions, while limiting radiation expo-sure to healthy tissue. However, fundamental differences between TRT and conventional radiotherapy make it impossible to directly extrapolate the biological effects from conventional radiotherapy to TRT. In this review, we present a comprehensive overview of studies investigating the immunomodulatory effects of TRT and the efficacy of combined TRT-ICI treatment. Preclinical studies have evaluated a variety of murine cancer models in which a- or (3-emitting radionuclides were directed to a diverse set of targets. In addition, clinical trials are ongoing to assess safety and efficacy of combined TRT-ICI in patients with cancer. Taken together, research indicates that combining TRT and ICI might improve therapeutic response in patients with cancer. Future research has to disclose what the optimal conditions are in terms of dose and treatment schedule to maximize the efficacy of this combined approach.

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