Frontiers in Nuclear Medicine (Apr 2024)

Immunological effects of radiopharmaceutical therapy

  • Amanda G. Shea,
  • Malick Bio Idrissou,
  • Ana Isabel Torres,
  • Tessa Chen,
  • Reiner Hernandez,
  • Reiner Hernandez,
  • Zachary S. Morris,
  • Zachary S. Morris,
  • Quaovi H. Sodji,
  • Quaovi H. Sodji

DOI
https://doi.org/10.3389/fnume.2024.1331364
Journal volume & issue
Vol. 4

Abstract

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Radiation therapy (RT) is a pillar of cancer therapy used by more than half of all cancer patients. Clinically, RT is mostly delivered as external beam radiation therapy (EBRT). However, the scope of EBRT is limited in the metastatic setting, where all sites of disease need to be irradiated. Such a limitation is attributed to radiation-induced toxicities, for example on bone marrow and hematologic toxicities, resulting from a large EBRT field. Radiopharmaceutical therapy (RPT) has emerged as an alternative to EBRT for the irradiation of all sites of metastatic disease. While RPT can reduce tumor burden, it can also impact the immune system and anti-tumor immunity. Understanding these effects is crucial for predicting and managing treatment-related hematological toxicities and optimizing their integration with other therapeutic modalities, such as immunotherapies. Here, we review the immunomodulatory effects of α- and β-particle emitter-based RPT on various immune cell lines, such as CD8+ and CD4+ T cells, natural killer (NK) cells, and regulatory T (Treg) cells. We briefly discuss Auger electron-emitter (AEE)-based RPT, and finally, we highlight the combination of RPT with immune checkpoint inhibitors, which may offer potential therapeutic synergies for patients with metastatic cancers.

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