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 |
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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 & 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. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c508t-46543b218e9bbeb7a89bbfd5e849a4ece25113d5dc683ca9abd78397726d0d883</citedby><cites>FETCH-LOGICAL-c508t-46543b218e9bbeb7a89bbfd5e849a4ece25113d5dc683ca9abd78397726d0d883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0360301611035012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26324253$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22300564$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22149476$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><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><title>Decreased Risk of Radiation Pneumonitis With Incidental Concurrent Use of Angiotensin-Converting Enzyme Inhibitors and Thoracic Radiation Therapy</title><title>International journal of radiation oncology, biology, physics</title><addtitle>Int J Radiat Oncol Biol Phys</addtitle><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.</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 & 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 & 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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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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