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Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience

Background: The safety impact of radiotherapy (RT) timing relative to immune checkpoint inhibitors (ICIs) for advanced non-small-cell lung cancer (NSCLC) is unclear. We investigated if RT within 14 days (Interval 1) and 90 days (Interval 2) of ICI use is associated with toxicities compared to RT out...

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Autores principales: Tjong, Michael C., Ragulojan, Malavan, Poon, Ian, Louie, Alexander V., Cheng, Susanna Y., Doherty, Mark, Zhang, Liying, Ung, Yee, Cheung, Patrick, Cheema, Parneet K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775081/
https://www.ncbi.nlm.nih.gov/pubmed/35049695
http://dx.doi.org/10.3390/curroncol29010021
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author Tjong, Michael C.
Ragulojan, Malavan
Poon, Ian
Louie, Alexander V.
Cheng, Susanna Y.
Doherty, Mark
Zhang, Liying
Ung, Yee
Cheung, Patrick
Cheema, Parneet K.
author_facet Tjong, Michael C.
Ragulojan, Malavan
Poon, Ian
Louie, Alexander V.
Cheng, Susanna Y.
Doherty, Mark
Zhang, Liying
Ung, Yee
Cheung, Patrick
Cheema, Parneet K.
author_sort Tjong, Michael C.
collection PubMed
description Background: The safety impact of radiotherapy (RT) timing relative to immune checkpoint inhibitors (ICIs) for advanced non-small-cell lung cancer (NSCLC) is unclear. We investigated if RT within 14 days (Interval 1) and 90 days (Interval 2) of ICI use is associated with toxicities compared to RT outside these intervals. Methods: Advanced NSCLC patients treated with both RT and ICIs were reviewed. Toxicities were graded as per CTCAE v4.0 and attributed to either ICIs or RT by clinicians. Associations between RT timing and Grade ≥2 toxicities were analyzed using logistic regression models adjusted for patient, disease, and treatment factors (α = 0.05). Results: Sixty-four patients were identified. Twenty received RT within Interval 1 and 40 within Interval 2. There were 20 Grade ≥2 toxicities in 18 (28%) patients; pneumonitis (6) and nausea (2) were most prevalent. One treatment-related death (immune encephalitis) was observed. Rates of patients with Grade ≥2 toxicities were 35%/25% in the group with/without RT within Interval 1 and 30%/25% in the group with/without RT within Interval 2. No significant association between RT timing relative to ICI use period and Grade ≥2 toxicities was observed. Conclusion: Albeit limited by the small sample size, the result suggested that pausing ICIs around RT use may not be necessary.
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spelling pubmed-87750812022-01-21 Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience Tjong, Michael C. Ragulojan, Malavan Poon, Ian Louie, Alexander V. Cheng, Susanna Y. Doherty, Mark Zhang, Liying Ung, Yee Cheung, Patrick Cheema, Parneet K. Curr Oncol Article Background: The safety impact of radiotherapy (RT) timing relative to immune checkpoint inhibitors (ICIs) for advanced non-small-cell lung cancer (NSCLC) is unclear. We investigated if RT within 14 days (Interval 1) and 90 days (Interval 2) of ICI use is associated with toxicities compared to RT outside these intervals. Methods: Advanced NSCLC patients treated with both RT and ICIs were reviewed. Toxicities were graded as per CTCAE v4.0 and attributed to either ICIs or RT by clinicians. Associations between RT timing and Grade ≥2 toxicities were analyzed using logistic regression models adjusted for patient, disease, and treatment factors (α = 0.05). Results: Sixty-four patients were identified. Twenty received RT within Interval 1 and 40 within Interval 2. There were 20 Grade ≥2 toxicities in 18 (28%) patients; pneumonitis (6) and nausea (2) were most prevalent. One treatment-related death (immune encephalitis) was observed. Rates of patients with Grade ≥2 toxicities were 35%/25% in the group with/without RT within Interval 1 and 30%/25% in the group with/without RT within Interval 2. No significant association between RT timing relative to ICI use period and Grade ≥2 toxicities was observed. Conclusion: Albeit limited by the small sample size, the result suggested that pausing ICIs around RT use may not be necessary. MDPI 2022-01-07 /pmc/articles/PMC8775081/ /pubmed/35049695 http://dx.doi.org/10.3390/curroncol29010021 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tjong, Michael C.
Ragulojan, Malavan
Poon, Ian
Louie, Alexander V.
Cheng, Susanna Y.
Doherty, Mark
Zhang, Liying
Ung, Yee
Cheung, Patrick
Cheema, Parneet K.
Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title_full Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title_fullStr Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title_full_unstemmed Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title_short Safety Related to the Timing of Radiotherapy and Immune Checkpoint Inhibitors in Patients with Advanced Non-Small Cell Lung Cancer: A Single Institutional Experience
title_sort safety related to the timing of radiotherapy and immune checkpoint inhibitors in patients with advanced non-small cell lung cancer: a single institutional experience
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775081/
https://www.ncbi.nlm.nih.gov/pubmed/35049695
http://dx.doi.org/10.3390/curroncol29010021
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