Toxicity of radiation and immunotherapy combinations

Purpose: Although immunotherapy is a rapidly emerging modality for cancer care, there have been multiple reports of fatal toxicities. There have also been cases of treatment-related deaths with combined non-immunotherapeutic biologic compounds with radiation therapy. Thus, provision of summative inf...

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Main Authors: Vivek Verma, MD, Taylor R. Cushman, BS, Chad Tang, MD, James W. Welsh, MD
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Advances in Radiation Oncology
Online Access:http://www.sciencedirect.com/science/article/pii/S2452109418301337
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spelling doaj-87d33d4553a64736a6236e0033a196ab2020-11-24T23:42:45ZengElsevierAdvances in Radiation Oncology2452-10942018-10-0134506511Toxicity of radiation and immunotherapy combinationsVivek Verma, MD0Taylor R. Cushman, BS1Chad Tang, MD2James W. Welsh, MD3Department of Radiation Oncology, Allegheny General Hospital, Pittsburgh, PennsylvaniaDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TexasDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, TexasDepartment of Radiation Oncology, University of Texas MD Anderson Cancer Center, Houston, Texas; Corresponding author. Department of Radiation Oncology, Unit 97, University of Texas, MD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030.Purpose: Although immunotherapy is a rapidly emerging modality for cancer care, there have been multiple reports of fatal toxicities. There have also been cases of treatment-related deaths with combined non-immunotherapeutic biologic compounds with radiation therapy. Thus, provision of summative information appraising the safety of combinatorial immunotherapy and radiation therapy (iRT) is imperative. Because this has not been well characterized, this review summarizes the available evidence to date. Methods and materials: Owing to the heterogeneity and relatively low quantity of published reports, this review was conducted in a narrative rather than systematic format. Results: The results of combined iRT, both concurrent and sequential, are discussed for oncologic therapy of the brain, lung, liver, and prostate. Most evidence is from small samples and shorter follow-up but does consist of multiple prospective publications. Most data exist for ipilimumab, with programmed cell death -1 inhibitors emerging in more recent years. With 2 large phase 3 trials as exceptions, there were no instances of iRT-related deaths across all discussed studies. Altogether, grade 3 to 4 toxicities were relatively low in frequency; of the studies that compared iRT with an “immunotherapy only” or “RT only” cohort, none documented a clear increase in high-grade adverse events with combined-modality management. Conclusions: Despite the low quantity of data, combined iRT offers encouraging safety profiles. There is no evidence that iRT produces an overt increase in high-grade toxicities. Further data, especially on concurrent iRT, are anticipated from numerous iRT trials that are currently ongoing worldwide.http://www.sciencedirect.com/science/article/pii/S2452109418301337
collection DOAJ
language English
format Article
sources DOAJ
author Vivek Verma, MD
Taylor R. Cushman, BS
Chad Tang, MD
James W. Welsh, MD
spellingShingle Vivek Verma, MD
Taylor R. Cushman, BS
Chad Tang, MD
James W. Welsh, MD
Toxicity of radiation and immunotherapy combinations
Advances in Radiation Oncology
author_facet Vivek Verma, MD
Taylor R. Cushman, BS
Chad Tang, MD
James W. Welsh, MD
author_sort Vivek Verma, MD
title Toxicity of radiation and immunotherapy combinations
title_short Toxicity of radiation and immunotherapy combinations
title_full Toxicity of radiation and immunotherapy combinations
title_fullStr Toxicity of radiation and immunotherapy combinations
title_full_unstemmed Toxicity of radiation and immunotherapy combinations
title_sort toxicity of radiation and immunotherapy combinations
publisher Elsevier
series Advances in Radiation Oncology
issn 2452-1094
publishDate 2018-10-01
description Purpose: Although immunotherapy is a rapidly emerging modality for cancer care, there have been multiple reports of fatal toxicities. There have also been cases of treatment-related deaths with combined non-immunotherapeutic biologic compounds with radiation therapy. Thus, provision of summative information appraising the safety of combinatorial immunotherapy and radiation therapy (iRT) is imperative. Because this has not been well characterized, this review summarizes the available evidence to date. Methods and materials: Owing to the heterogeneity and relatively low quantity of published reports, this review was conducted in a narrative rather than systematic format. Results: The results of combined iRT, both concurrent and sequential, are discussed for oncologic therapy of the brain, lung, liver, and prostate. Most evidence is from small samples and shorter follow-up but does consist of multiple prospective publications. Most data exist for ipilimumab, with programmed cell death -1 inhibitors emerging in more recent years. With 2 large phase 3 trials as exceptions, there were no instances of iRT-related deaths across all discussed studies. Altogether, grade 3 to 4 toxicities were relatively low in frequency; of the studies that compared iRT with an “immunotherapy only” or “RT only” cohort, none documented a clear increase in high-grade adverse events with combined-modality management. Conclusions: Despite the low quantity of data, combined iRT offers encouraging safety profiles. There is no evidence that iRT produces an overt increase in high-grade toxicities. Further data, especially on concurrent iRT, are anticipated from numerous iRT trials that are currently ongoing worldwide.
url http://www.sciencedirect.com/science/article/pii/S2452109418301337
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