Decreased Risk of Radiation Pneumonitis With Incidental Concurrent Use of Angiotensin-Converting Enzyme Inhibitors and Thoracic Radiation Therapy

Purpose Angiotensin-converting enzyme (ACE) inhibitors have been shown to mitigate radiation-induced lung injury in preclinical models. The aim of this study was to evaluate whether ACE inhibitors decrease the risk of radiation pneumonitis in lung cancer patients receiving thoracic irradiation. Meth...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2012-09, Vol.84 (1), p.238-243
Hauptverfasser: Kharofa, Jordan, M.D, Cohen, Eric P., M.D, Tomic, Rade, M.D, Xiang, Qun, M.S, Gore, Elizabeth, M.D
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container_issue 1
container_start_page 238
container_title International journal of radiation oncology, biology, physics
container_volume 84
creator Kharofa, Jordan, M.D
Cohen, Eric P., M.D
Tomic, Rade, M.D
Xiang, Qun, M.S
Gore, Elizabeth, M.D
description Purpose Angiotensin-converting enzyme (ACE) inhibitors have been shown to mitigate radiation-induced lung injury in preclinical models. The aim of this study was to evaluate whether ACE inhibitors decrease the risk of radiation pneumonitis in lung cancer patients receiving thoracic irradiation. Methods and Materials Patients with Stage I through III small-cell and non-small-cell lung cancer treated definitively with radiation from 2004–2009 at the Clement J. Zablocki Veterans Affairs Medical Center were retrospectively reviewed. Acute pulmonary toxicity was quantified within 6 months of completion of treatment according to the Common Terminology Criteria for Adverse Events version 4. The use of ACE inhibitors, nonsteroidal anti-inflammatory drugs, inhaled glucocorticosteroids, statins, and angiotensin receptor blockers; dose–volume histogram parameters; and patient factors were assessed for association with Grade 2 or higher pneumonitis. Results A total of 162 patients met the criteria for inclusion. The majority of patients had Stage III disease (64%) and received concurrent chemotherapy (61%). Sixty-two patients were identified as ACE inhibitor users (38%). All patients had acceptable radiation plans based on dose–volume histogram constraints (V20 [volume of lung receiving at least 20 Gy] ≤37% and mean lung dose ≤20 Gy) with the exception of 2 patients who did not meet both criteria. Grade 2 or higher pulmonary toxicity occurred in 12 patients (7.4%). The rate of Grade 2 or higher pneumonitis was lower in ACE inhibitor users vs. nonusers (2% vs. 11%, p = 0.032). Rates of Grade 2 or higher pneumonitis were significantly increased in patients aged greater than 70 years (16% vs. 2%, p = 0.005) or in whom V5 (volume of lung receiving at least 5 Gy) was 50% or greater (13% vs. 4%, p = 0.04). V10 (volume of lung receiving at least 10 Gy), V20, V30 (volume of lung receiving at least 30 Gy), and mean lung dose were not independently associated with Grade 2 or higher pneumonitis. Conclusion ACE inhibitors may decrease the incidence of radiation pneumonitis in patients receiving thoracic radiation for lung cancer. These findings are consistent with preclinical evidence and should be prospectively evaluated.
doi_str_mv 10.1016/j.ijrobp.2011.11.013
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The aim of this study was to evaluate whether ACE inhibitors decrease the risk of radiation pneumonitis in lung cancer patients receiving thoracic irradiation. Methods and Materials Patients with Stage I through III small-cell and non-small-cell lung cancer treated definitively with radiation from 2004–2009 at the Clement J. Zablocki Veterans Affairs Medical Center were retrospectively reviewed. Acute pulmonary toxicity was quantified within 6 months of completion of treatment according to the Common Terminology Criteria for Adverse Events version 4. The use of ACE inhibitors, nonsteroidal anti-inflammatory drugs, inhaled glucocorticosteroids, statins, and angiotensin receptor blockers; dose–volume histogram parameters; and patient factors were assessed for association with Grade 2 or higher pneumonitis. Results A total of 162 patients met the criteria for inclusion. The majority of patients had Stage III disease (64%) and received concurrent chemotherapy (61%). Sixty-two patients were identified as ACE inhibitor users (38%). All patients had acceptable radiation plans based on dose–volume histogram constraints (V20 [volume of lung receiving at least 20 Gy] ≤37% and mean lung dose ≤20 Gy) with the exception of 2 patients who did not meet both criteria. Grade 2 or higher pulmonary toxicity occurred in 12 patients (7.4%). The rate of Grade 2 or higher pneumonitis was lower in ACE inhibitor users vs. nonusers (2% vs. 11%, p = 0.032). Rates of Grade 2 or higher pneumonitis were significantly increased in patients aged greater than 70 years (16% vs. 2%, p = 0.005) or in whom V5 (volume of lung receiving at least 5 Gy) was 50% or greater (13% vs. 4%, p = 0.04). V10 (volume of lung receiving at least 10 Gy), V20, V30 (volume of lung receiving at least 30 Gy), and mean lung dose were not independently associated with Grade 2 or higher pneumonitis. Conclusion ACE inhibitors may decrease the incidence of radiation pneumonitis in patients receiving thoracic radiation for lung cancer. These findings are consistent with preclinical evidence and should be prospectively evaluated.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2011.11.013</identifier><identifier>PMID: 22300564</identifier><identifier>CODEN: IOBPD3</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>ACE inhibitors ; Aged ; ANGIOTENSIN ; Angiotensin receptors ; Angiotensin-converting enzyme inhibitors ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Antiinflammatory agents ; Biological and medical sciences ; Captopril - therapeutic use ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - pathology ; Carcinoma, Non-Small-Cell Lung - radiotherapy ; CHEMOTHERAPY ; Corticoids ; ELDERLY PEOPLE ; ENZYME INHIBITORS ; ENZYMES ; HEALTH HAZARDS ; Hematology, Oncology and Palliative Medicine ; Humans ; Incidence ; INFLAMMATION ; Injuries ; IRRADIATION ; Lisinopril - therapeutic use ; Lung - radiation effects ; Lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - pathology ; Lung Neoplasms - radiotherapy ; LUNGS ; Male ; Medical sciences ; Middle Aged ; NEOPLASMS ; PATIENTS ; Peptidyl-dipeptidase A ; Pneumology ; PNEUMONITIS ; Pulmonary toxicity ; Radiation ; RADIATION DOSES ; RADIATION INJURIES ; Radiation pneumonitis ; Radiation Pneumonitis - epidemiology ; Radiation Pneumonitis - etiology ; Radiation Pneumonitis - pathology ; Radiation Pneumonitis - prevention &amp; control ; Radiation-induced lung injury ; Radiology ; RADIOLOGY AND NUCLEAR MEDICINE ; RADIOTHERAPY ; RECEPTORS ; Retrospective Studies ; Small Cell Lung Carcinoma - drug therapy ; Small Cell Lung Carcinoma - pathology ; Small Cell Lung Carcinoma - radiotherapy ; statins ; Thorax ; TOXICITY ; Tumor Burden ; Tumors of the respiratory system and mediastinum</subject><ispartof>International journal of radiation oncology, biology, physics, 2012-09, Vol.84 (1), p.238-243</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. 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The aim of this study was to evaluate whether ACE inhibitors decrease the risk of radiation pneumonitis in lung cancer patients receiving thoracic irradiation. Methods and Materials Patients with Stage I through III small-cell and non-small-cell lung cancer treated definitively with radiation from 2004–2009 at the Clement J. Zablocki Veterans Affairs Medical Center were retrospectively reviewed. Acute pulmonary toxicity was quantified within 6 months of completion of treatment according to the Common Terminology Criteria for Adverse Events version 4. The use of ACE inhibitors, nonsteroidal anti-inflammatory drugs, inhaled glucocorticosteroids, statins, and angiotensin receptor blockers; dose–volume histogram parameters; and patient factors were assessed for association with Grade 2 or higher pneumonitis. Results A total of 162 patients met the criteria for inclusion. The majority of patients had Stage III disease (64%) and received concurrent chemotherapy (61%). Sixty-two patients were identified as ACE inhibitor users (38%). All patients had acceptable radiation plans based on dose–volume histogram constraints (V20 [volume of lung receiving at least 20 Gy] ≤37% and mean lung dose ≤20 Gy) with the exception of 2 patients who did not meet both criteria. Grade 2 or higher pulmonary toxicity occurred in 12 patients (7.4%). The rate of Grade 2 or higher pneumonitis was lower in ACE inhibitor users vs. nonusers (2% vs. 11%, p = 0.032). Rates of Grade 2 or higher pneumonitis were significantly increased in patients aged greater than 70 years (16% vs. 2%, p = 0.005) or in whom V5 (volume of lung receiving at least 5 Gy) was 50% or greater (13% vs. 4%, p = 0.04). V10 (volume of lung receiving at least 10 Gy), V20, V30 (volume of lung receiving at least 30 Gy), and mean lung dose were not independently associated with Grade 2 or higher pneumonitis. Conclusion ACE inhibitors may decrease the incidence of radiation pneumonitis in patients receiving thoracic radiation for lung cancer. These findings are consistent with preclinical evidence and should be prospectively evaluated.</description><subject>ACE inhibitors</subject><subject>Aged</subject><subject>ANGIOTENSIN</subject><subject>Angiotensin receptors</subject><subject>Angiotensin-converting enzyme inhibitors</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Antiinflammatory agents</subject><subject>Biological and medical sciences</subject><subject>Captopril - therapeutic use</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Carcinoma, Non-Small-Cell Lung - radiotherapy</subject><subject>CHEMOTHERAPY</subject><subject>Corticoids</subject><subject>ELDERLY PEOPLE</subject><subject>ENZYME INHIBITORS</subject><subject>ENZYMES</subject><subject>HEALTH HAZARDS</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Incidence</subject><subject>INFLAMMATION</subject><subject>Injuries</subject><subject>IRRADIATION</subject><subject>Lisinopril - therapeutic use</subject><subject>Lung - radiation effects</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - pathology</subject><subject>Lung Neoplasms - radiotherapy</subject><subject>LUNGS</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>NEOPLASMS</subject><subject>PATIENTS</subject><subject>Peptidyl-dipeptidase A</subject><subject>Pneumology</subject><subject>PNEUMONITIS</subject><subject>Pulmonary toxicity</subject><subject>Radiation</subject><subject>RADIATION DOSES</subject><subject>RADIATION INJURIES</subject><subject>Radiation pneumonitis</subject><subject>Radiation Pneumonitis - epidemiology</subject><subject>Radiation Pneumonitis - etiology</subject><subject>Radiation Pneumonitis - pathology</subject><subject>Radiation Pneumonitis - prevention &amp; control</subject><subject>Radiation-induced lung injury</subject><subject>Radiology</subject><subject>RADIOLOGY AND NUCLEAR MEDICINE</subject><subject>RADIOTHERAPY</subject><subject>RECEPTORS</subject><subject>Retrospective Studies</subject><subject>Small Cell Lung Carcinoma - drug therapy</subject><subject>Small Cell Lung Carcinoma - pathology</subject><subject>Small Cell Lung Carcinoma - radiotherapy</subject><subject>statins</subject><subject>Thorax</subject><subject>TOXICITY</subject><subject>Tumor Burden</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkltrFDEUxwdR7Fr9BiIBEXyZNZe5vghlrVooKHWLvoVMcqZ7trPJNskU1m_hNzbDrBd8EQKHkN__XPI_Wfac0SWjrHqzXeLWu26_5JSxZTqUiQfZgjV1m4uy_PYwW1BR0Vwk-CR7EsKW0kTWxePshHNBaVkVi-zHO9AeVABDrjDcEteTK2VQRXSWfLYw7pzFiIF8xbghF1ajARvVQFbO6tH7dCHXASbdmb1BF8EGtHl6vQcf0d6Qc_v9sIMk3WCH0flAlDVkvXFeadR_VVtvwKv94Wn2qFdDgGfHeJpdvz9frz7ml58-XKzOLnNd0ibmRVUWouOsgbbroKtVk2JvSmiKVhWggZeMCVMaXTVCq1Z1pm5EW9e8MtQ0jTjNXs55XYgog8YIeqOdtaCj5JwVbVFXiXo9U3vv7kYIUe4waBgGZcGNQTLaitSKEHVCixnV3oXgoZd7jzvlDwmSk2VyK2fL5GSZTCdZlmQvjhXGbgfmt-iXRwl4dQRU0GrovUouhD9cJXjByynR25mD9Gv3CH4aCqwGg36ayTj8Xyf_JtADWkw1b-EAYetGb5MjksnAJZVfpvWatosxKkrKuPgJFEHNLw</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Kharofa, Jordan, M.D</creator><creator>Cohen, Eric P., M.D</creator><creator>Tomic, Rade, M.D</creator><creator>Xiang, Qun, M.S</creator><creator>Gore, Elizabeth, M.D</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U7</scope><scope>C1K</scope><scope>OTOTI</scope></search><sort><creationdate>20120901</creationdate><title>Decreased Risk of Radiation Pneumonitis With Incidental Concurrent Use of Angiotensin-Converting Enzyme Inhibitors and Thoracic Radiation Therapy</title><author>Kharofa, Jordan, M.D ; Cohen, Eric P., M.D ; Tomic, Rade, M.D ; Xiang, Qun, M.S ; Gore, Elizabeth, M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c508t-46543b218e9bbeb7a89bbfd5e849a4ece25113d5dc683ca9abd78397726d0d883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>ACE inhibitors</topic><topic>Aged</topic><topic>ANGIOTENSIN</topic><topic>Angiotensin receptors</topic><topic>Angiotensin-converting enzyme inhibitors</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Antiinflammatory agents</topic><topic>Biological and medical sciences</topic><topic>Captopril - therapeutic use</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Carcinoma, Non-Small-Cell Lung - radiotherapy</topic><topic>CHEMOTHERAPY</topic><topic>Corticoids</topic><topic>ELDERLY PEOPLE</topic><topic>ENZYME INHIBITORS</topic><topic>ENZYMES</topic><topic>HEALTH HAZARDS</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Incidence</topic><topic>INFLAMMATION</topic><topic>Injuries</topic><topic>IRRADIATION</topic><topic>Lisinopril - therapeutic use</topic><topic>Lung - radiation effects</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - pathology</topic><topic>Lung Neoplasms - radiotherapy</topic><topic>LUNGS</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>NEOPLASMS</topic><topic>PATIENTS</topic><topic>Peptidyl-dipeptidase A</topic><topic>Pneumology</topic><topic>PNEUMONITIS</topic><topic>Pulmonary toxicity</topic><topic>Radiation</topic><topic>RADIATION DOSES</topic><topic>RADIATION INJURIES</topic><topic>Radiation pneumonitis</topic><topic>Radiation Pneumonitis - epidemiology</topic><topic>Radiation Pneumonitis - etiology</topic><topic>Radiation Pneumonitis - pathology</topic><topic>Radiation Pneumonitis - prevention &amp; control</topic><topic>Radiation-induced lung injury</topic><topic>Radiology</topic><topic>RADIOLOGY AND NUCLEAR MEDICINE</topic><topic>RADIOTHERAPY</topic><topic>RECEPTORS</topic><topic>Retrospective Studies</topic><topic>Small Cell Lung Carcinoma - drug therapy</topic><topic>Small Cell Lung Carcinoma - pathology</topic><topic>Small Cell Lung Carcinoma - radiotherapy</topic><topic>statins</topic><topic>Thorax</topic><topic>TOXICITY</topic><topic>Tumor Burden</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kharofa, Jordan, M.D</creatorcontrib><creatorcontrib>Cohen, Eric P., M.D</creatorcontrib><creatorcontrib>Tomic, Rade, M.D</creatorcontrib><creatorcontrib>Xiang, Qun, M.S</creatorcontrib><creatorcontrib>Gore, Elizabeth, M.D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>OSTI.GOV</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kharofa, Jordan, M.D</au><au>Cohen, Eric P., M.D</au><au>Tomic, Rade, M.D</au><au>Xiang, Qun, M.S</au><au>Gore, Elizabeth, M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased Risk of Radiation Pneumonitis With Incidental Concurrent Use of Angiotensin-Converting Enzyme Inhibitors and Thoracic Radiation Therapy</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>84</volume><issue>1</issue><spage>238</spage><epage>243</epage><pages>238-243</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><coden>IOBPD3</coden><abstract>Purpose Angiotensin-converting enzyme (ACE) inhibitors have been shown to mitigate radiation-induced lung injury in preclinical models. The aim of this study was to evaluate whether ACE inhibitors decrease the risk of radiation pneumonitis in lung cancer patients receiving thoracic irradiation. Methods and Materials Patients with Stage I through III small-cell and non-small-cell lung cancer treated definitively with radiation from 2004–2009 at the Clement J. Zablocki Veterans Affairs Medical Center were retrospectively reviewed. Acute pulmonary toxicity was quantified within 6 months of completion of treatment according to the Common Terminology Criteria for Adverse Events version 4. The use of ACE inhibitors, nonsteroidal anti-inflammatory drugs, inhaled glucocorticosteroids, statins, and angiotensin receptor blockers; dose–volume histogram parameters; and patient factors were assessed for association with Grade 2 or higher pneumonitis. Results A total of 162 patients met the criteria for inclusion. The majority of patients had Stage III disease (64%) and received concurrent chemotherapy (61%). Sixty-two patients were identified as ACE inhibitor users (38%). All patients had acceptable radiation plans based on dose–volume histogram constraints (V20 [volume of lung receiving at least 20 Gy] ≤37% and mean lung dose ≤20 Gy) with the exception of 2 patients who did not meet both criteria. Grade 2 or higher pulmonary toxicity occurred in 12 patients (7.4%). The rate of Grade 2 or higher pneumonitis was lower in ACE inhibitor users vs. nonusers (2% vs. 11%, p = 0.032). Rates of Grade 2 or higher pneumonitis were significantly increased in patients aged greater than 70 years (16% vs. 2%, p = 0.005) or in whom V5 (volume of lung receiving at least 5 Gy) was 50% or greater (13% vs. 4%, p = 0.04). V10 (volume of lung receiving at least 10 Gy), V20, V30 (volume of lung receiving at least 30 Gy), and mean lung dose were not independently associated with Grade 2 or higher pneumonitis. Conclusion ACE inhibitors may decrease the incidence of radiation pneumonitis in patients receiving thoracic radiation for lung cancer. These findings are consistent with preclinical evidence and should be prospectively evaluated.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22300564</pmid><doi>10.1016/j.ijrobp.2011.11.013</doi><tpages>6</tpages></addata></record>
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ispartof International journal of radiation oncology, biology, physics, 2012-09, Vol.84 (1), p.238-243
issn 0360-3016
1879-355X
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subjects ACE inhibitors
Aged
ANGIOTENSIN
Angiotensin receptors
Angiotensin-converting enzyme inhibitors
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Antiinflammatory agents
Biological and medical sciences
Captopril - therapeutic use
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - pathology
Carcinoma, Non-Small-Cell Lung - radiotherapy
CHEMOTHERAPY
Corticoids
ELDERLY PEOPLE
ENZYME INHIBITORS
ENZYMES
HEALTH HAZARDS
Hematology, Oncology and Palliative Medicine
Humans
Incidence
INFLAMMATION
Injuries
IRRADIATION
Lisinopril - therapeutic use
Lung - radiation effects
Lung cancer
Lung Neoplasms - drug therapy
Lung Neoplasms - pathology
Lung Neoplasms - radiotherapy
LUNGS
Male
Medical sciences
Middle Aged
NEOPLASMS
PATIENTS
Peptidyl-dipeptidase A
Pneumology
PNEUMONITIS
Pulmonary toxicity
Radiation
RADIATION DOSES
RADIATION INJURIES
Radiation pneumonitis
Radiation Pneumonitis - epidemiology
Radiation Pneumonitis - etiology
Radiation Pneumonitis - pathology
Radiation Pneumonitis - prevention & control
Radiation-induced lung injury
Radiology
RADIOLOGY AND NUCLEAR MEDICINE
RADIOTHERAPY
RECEPTORS
Retrospective Studies
Small Cell Lung Carcinoma - drug therapy
Small Cell Lung Carcinoma - pathology
Small Cell Lung Carcinoma - radiotherapy
statins
Thorax
TOXICITY
Tumor Burden
Tumors of the respiratory system and mediastinum
title Decreased Risk of Radiation Pneumonitis With Incidental Concurrent Use of Angiotensin-Converting Enzyme Inhibitors and Thoracic Radiation Therapy
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