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Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy

PURPOSE: Radiation therapy (RT) and nivolumab are standard therapies for a wide range of advanced and metastatic cancers, yet little is known about the toxicity profile of their combined treatment. The rate of grade ≥3 toxicities from nivolumab monotherapy and radiation-only palliative treatments ha...

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Autores principales: Amin, Neha P., Zainib, Maliha, Parker, Sean M., Agarwal, Manuj, Mattes, Malcolm D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128090/
https://www.ncbi.nlm.nih.gov/pubmed/30202808
http://dx.doi.org/10.1016/j.adro.2018.04.015
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author Amin, Neha P.
Zainib, Maliha
Parker, Sean M.
Agarwal, Manuj
Mattes, Malcolm D.
author_facet Amin, Neha P.
Zainib, Maliha
Parker, Sean M.
Agarwal, Manuj
Mattes, Malcolm D.
author_sort Amin, Neha P.
collection PubMed
description PURPOSE: Radiation therapy (RT) and nivolumab are standard therapies for a wide range of advanced and metastatic cancers, yet little is known about the toxicity profile of their combined treatment. The rate of grade ≥3 toxicities from nivolumab monotherapy and radiation-only palliative treatments has been reported at 10% to 18% and 0% to 26%, respectively. We reviewed our experience to assess the acute toxicity profile of concurrent RT-nivolumab. METHODS AND MATERIALS: A retrospective review of all consecutive patients from January 2015 to May 2017 who received concurrent RT-nivolumab was conducted at 4 separate centers. Concurrent RT-nivolumab was defined as RT completed between 3 days prior to initial nivolumab infusion and 28 days after the last nivolumab infusion. RESULTS: Of the 261 patients who received nivolumab, 46 (17.6%) had concurrent RT to 67 treatment sites. The median follow-up was 3.3 months (interquartile range, 1.7-6.1 months) and the 1-year overall survival rate was 22%. For the 11 of 46 patients (24%) who were alive at last analysis, the median follow-up was 12.8 months (interquartile range, 8.3-14.9 months). The most common histology, RT prescription, and treatment site were non-small cell lung cancer (23 of 46 patients; 50%), 30 Gy in 10 fractions (24 of 67 patients; 35.8%), and abdomen/pelvis (16 of 67 patients; 24%), respectively. Four patients with melanoma had concurrent ipilimumab and were removed from the final toxicity analysis of RT-nivolumab. Within 3 months of treatment with RT-nivolumab, 4 of 42 patients (9.5%) experienced grade 3 toxicity and 2 of these patients' toxicities were attributed specifically to the addition of RT: grade 3 hearing loss after whole brain RT and grade 3 pancreatitis after stereotactic body RT to the left adrenal gland. One death from transaminitis was attributed to nivolumab alone because the RT field did not encompass the liver. CONCLUSIONS: Concurrent RT-nivolumab did not appear to increase the toxicity profile from the previously reported toxicity rates from nivolumab or radiation alone.
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spelling pubmed-61280902018-09-10 Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy Amin, Neha P. Zainib, Maliha Parker, Sean M. Agarwal, Manuj Mattes, Malcolm D. Adv Radiat Oncol Toxicity Report PURPOSE: Radiation therapy (RT) and nivolumab are standard therapies for a wide range of advanced and metastatic cancers, yet little is known about the toxicity profile of their combined treatment. The rate of grade ≥3 toxicities from nivolumab monotherapy and radiation-only palliative treatments has been reported at 10% to 18% and 0% to 26%, respectively. We reviewed our experience to assess the acute toxicity profile of concurrent RT-nivolumab. METHODS AND MATERIALS: A retrospective review of all consecutive patients from January 2015 to May 2017 who received concurrent RT-nivolumab was conducted at 4 separate centers. Concurrent RT-nivolumab was defined as RT completed between 3 days prior to initial nivolumab infusion and 28 days after the last nivolumab infusion. RESULTS: Of the 261 patients who received nivolumab, 46 (17.6%) had concurrent RT to 67 treatment sites. The median follow-up was 3.3 months (interquartile range, 1.7-6.1 months) and the 1-year overall survival rate was 22%. For the 11 of 46 patients (24%) who were alive at last analysis, the median follow-up was 12.8 months (interquartile range, 8.3-14.9 months). The most common histology, RT prescription, and treatment site were non-small cell lung cancer (23 of 46 patients; 50%), 30 Gy in 10 fractions (24 of 67 patients; 35.8%), and abdomen/pelvis (16 of 67 patients; 24%), respectively. Four patients with melanoma had concurrent ipilimumab and were removed from the final toxicity analysis of RT-nivolumab. Within 3 months of treatment with RT-nivolumab, 4 of 42 patients (9.5%) experienced grade 3 toxicity and 2 of these patients' toxicities were attributed specifically to the addition of RT: grade 3 hearing loss after whole brain RT and grade 3 pancreatitis after stereotactic body RT to the left adrenal gland. One death from transaminitis was attributed to nivolumab alone because the RT field did not encompass the liver. CONCLUSIONS: Concurrent RT-nivolumab did not appear to increase the toxicity profile from the previously reported toxicity rates from nivolumab or radiation alone. Elsevier 2018-05-24 /pmc/articles/PMC6128090/ /pubmed/30202808 http://dx.doi.org/10.1016/j.adro.2018.04.015 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Toxicity Report
Amin, Neha P.
Zainib, Maliha
Parker, Sean M.
Agarwal, Manuj
Mattes, Malcolm D.
Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title_full Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title_fullStr Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title_full_unstemmed Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title_short Multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
title_sort multi-institutional report on toxicities of concurrent nivolumab and radiation therapy
topic Toxicity Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128090/
https://www.ncbi.nlm.nih.gov/pubmed/30202808
http://dx.doi.org/10.1016/j.adro.2018.04.015
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