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Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment

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, radiothera...

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Autores principales: Kleinendorst, Simone C., Oosterwijk, Egbert, Bussink, Johan, Westdorp, Harm, Konijnenberg, Mark W., Heskamp, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for Cancer Research 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433955/
https://www.ncbi.nlm.nih.gov/pubmed/35471557
http://dx.doi.org/10.1158/1078-0432.CCR-21-4332
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author Kleinendorst, Simone C.
Oosterwijk, Egbert
Bussink, Johan
Westdorp, Harm
Konijnenberg, Mark W.
Heskamp, Sandra
author_facet Kleinendorst, Simone C.
Oosterwijk, Egbert
Bussink, Johan
Westdorp, Harm
Konijnenberg, Mark W.
Heskamp, Sandra
author_sort Kleinendorst, Simone C.
collection PubMed
description 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 phenotype 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 exposure 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 α- or β-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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spelling pubmed-94339552023-01-05 Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment Kleinendorst, Simone C. Oosterwijk, Egbert Bussink, Johan Westdorp, Harm Konijnenberg, Mark W. Heskamp, Sandra Clin Cancer Res Reviews 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 phenotype 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 exposure 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 α- or β-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. American Association for Cancer Research 2022-09-01 2022-04-26 /pmc/articles/PMC9433955/ /pubmed/35471557 http://dx.doi.org/10.1158/1078-0432.CCR-21-4332 Text en ©2022 The Authors; Published by the American Association for Cancer Research https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) license.
spellingShingle Reviews
Kleinendorst, Simone C.
Oosterwijk, Egbert
Bussink, Johan
Westdorp, Harm
Konijnenberg, Mark W.
Heskamp, Sandra
Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title_full Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title_fullStr Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title_full_unstemmed Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title_short Combining Targeted Radionuclide Therapy and Immune Checkpoint Inhibition for Cancer Treatment
title_sort combining targeted radionuclide therapy and immune checkpoint inhibition for cancer treatment
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433955/
https://www.ncbi.nlm.nih.gov/pubmed/35471557
http://dx.doi.org/10.1158/1078-0432.CCR-21-4332
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