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Radiation necrosis in renal cell carcinoma brain metastases treated with checkpoint inhibitors and radiosurgery: An international multicenter study

BACKGROUND Patients with renal cell carcinoma (RCC) brain metastases are frequently treated with immune checkpoint inhibitors (ICIs) and stereotactic radiosurgery (SRS). However, data reporting on the risk of developing radiation necrosis (RN) are limited. METHODS RN rates were compared for concurre...

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Published in:Cancer 2022-04, Vol.128 (7), p.1429-1438
Main Authors: Lehrer, Eric J., Gurewitz, Jason, Bernstein, Kenneth, Patel, Dev, Kondziolka, Douglas, Niranjan, Ajay, Wei, Zhishuo, Lunsford, L. Dade, Malouff, Timothy D., Ruiz‐Garcia, Henry, Patel, Samir, Bonney, Phillip A., Hwang, Lindsay, Yu, Cheng, Zada, Gabriel, Mathieu, David, Trudel, Claire, Prasad, Rahul N., Palmer, Joshua D., Jones, Brianna M., Sharma, Sonam, Fakhoury, Kareem R., Rusthoven, Chad G., Deibert, Christopher P., Picozzi, Piero, Franzini, Andrea, Attuati, Luca, Lee, Cheng‐Chia, Yang, Huai‐Che, Ahluwalia, Manmeet S., Sheehan, Jason P., Trifiletti, Daniel M.
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cited_by cdi_FETCH-LOGICAL-c3937-83d7d4804e806bf87dfeca1ef6d4c9d7b3cf51c610d118ad0cf2f07c7ad5cce53
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container_end_page 1438
container_issue 7
container_start_page 1429
container_title Cancer
container_volume 128
creator Lehrer, Eric J.
Gurewitz, Jason
Bernstein, Kenneth
Patel, Dev
Kondziolka, Douglas
Niranjan, Ajay
Wei, Zhishuo
Lunsford, L. Dade
Malouff, Timothy D.
Ruiz‐Garcia, Henry
Patel, Samir
Bonney, Phillip A.
Hwang, Lindsay
Yu, Cheng
Zada, Gabriel
Mathieu, David
Trudel, Claire
Prasad, Rahul N.
Palmer, Joshua D.
Jones, Brianna M.
Sharma, Sonam
Fakhoury, Kareem R.
Rusthoven, Chad G.
Deibert, Christopher P.
Picozzi, Piero
Franzini, Andrea
Attuati, Luca
Lee, Cheng‐Chia
Yang, Huai‐Che
Ahluwalia, Manmeet S.
Sheehan, Jason P.
Trifiletti, Daniel M.
description BACKGROUND Patients with renal cell carcinoma (RCC) brain metastases are frequently treated with immune checkpoint inhibitors (ICIs) and stereotactic radiosurgery (SRS). However, data reporting on the risk of developing radiation necrosis (RN) are limited. METHODS RN rates were compared for concurrent therapy (ICI/SRS administration within 4 weeks of one another) and nonconcurrent therapy with the χ2 test. Univariable logistic regression was used to identify factors associated with developing RN. RESULTS Fifty patients (23 concurrent and 27 nonconcurrent) with 395 brain metastases were analyzed. The median follow‐up was 12.1 months; the median age was 65 years. The median margin dose was 20 Gy, and 4% underwent prior whole‐brain radiation therapy (WBRT). The median treated tumor volume was 3.32 cm3 (range, 0.06‐42.38 cm3); the median volume of normal brain tissue receiving a dose of 12 Gy or higher (V12 Gy) was 8.42 cm3 (range, 0.27‐111.22 cm3). Any‐grade RN occurred in 17.4% and 22.2% in the concurrent and nonconcurrent groups, respectively (P = .67). Symptomatic RN occurred in 4.3% and 14.8% in the concurrent and nonconcurrent groups, respectively (P = .23). Increased tumor volume during SRS (odds ratio [OR], 1.08; 95% confidence interval [CI], 1.01‐1.19; P = .04) was associated with developing RN, although V12 Gy (OR, 1.03; 95% CI, 0.99‐1.06; P = .06), concurrent therapy (OR, 0.74; 95% CI, 0.17‐2.30; P = .76), prior WBRT, and ICI agents were not statistically significant. CONCLUSIONS Symptomatic RN occurs in a minority of patients with RCC brain metastases treated with ICI/SRS. The majority of events were grade 1 to 3 and were managed medically. Concurrent ICI/SRS does not appear to increase this risk. Attempts to improve dose conformality (reduce V12) may be the most successful mitigation strategy in single‐fraction SRS. The concurrent administration of immune checkpoint inhibitors and stereotactic radiosurgery in patients with renal cell carcinoma brain metastases is safe and well tolerated. Symptomatic radiation necrosis occurred in
doi_str_mv 10.1002/cncr.34087
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Dade ; Malouff, Timothy D. ; Ruiz‐Garcia, Henry ; Patel, Samir ; Bonney, Phillip A. ; Hwang, Lindsay ; Yu, Cheng ; Zada, Gabriel ; Mathieu, David ; Trudel, Claire ; Prasad, Rahul N. ; Palmer, Joshua D. ; Jones, Brianna M. ; Sharma, Sonam ; Fakhoury, Kareem R. ; Rusthoven, Chad G. ; Deibert, Christopher P. ; Picozzi, Piero ; Franzini, Andrea ; Attuati, Luca ; Lee, Cheng‐Chia ; Yang, Huai‐Che ; Ahluwalia, Manmeet S. ; Sheehan, Jason P. ; Trifiletti, Daniel M.</creator><creatorcontrib>Lehrer, Eric J. ; Gurewitz, Jason ; Bernstein, Kenneth ; Patel, Dev ; Kondziolka, Douglas ; Niranjan, Ajay ; Wei, Zhishuo ; Lunsford, L. Dade ; Malouff, Timothy D. ; Ruiz‐Garcia, Henry ; Patel, Samir ; Bonney, Phillip A. ; Hwang, Lindsay ; Yu, Cheng ; Zada, Gabriel ; Mathieu, David ; Trudel, Claire ; Prasad, Rahul N. ; Palmer, Joshua D. ; Jones, Brianna M. ; Sharma, Sonam ; Fakhoury, Kareem R. ; Rusthoven, Chad G. ; Deibert, Christopher P. ; Picozzi, Piero ; Franzini, Andrea ; Attuati, Luca ; Lee, Cheng‐Chia ; Yang, Huai‐Che ; Ahluwalia, Manmeet S. ; Sheehan, Jason P. ; Trifiletti, Daniel M.</creatorcontrib><description>BACKGROUND Patients with renal cell carcinoma (RCC) brain metastases are frequently treated with immune checkpoint inhibitors (ICIs) and stereotactic radiosurgery (SRS). However, data reporting on the risk of developing radiation necrosis (RN) are limited. METHODS RN rates were compared for concurrent therapy (ICI/SRS administration within 4 weeks of one another) and nonconcurrent therapy with the χ2 test. Univariable logistic regression was used to identify factors associated with developing RN. RESULTS Fifty patients (23 concurrent and 27 nonconcurrent) with 395 brain metastases were analyzed. The median follow‐up was 12.1 months; the median age was 65 years. The median margin dose was 20 Gy, and 4% underwent prior whole‐brain radiation therapy (WBRT). The median treated tumor volume was 3.32 cm3 (range, 0.06‐42.38 cm3); the median volume of normal brain tissue receiving a dose of 12 Gy or higher (V12 Gy) was 8.42 cm3 (range, 0.27‐111.22 cm3). Any‐grade RN occurred in 17.4% and 22.2% in the concurrent and nonconcurrent groups, respectively (P = .67). Symptomatic RN occurred in 4.3% and 14.8% in the concurrent and nonconcurrent groups, respectively (P = .23). Increased tumor volume during SRS (odds ratio [OR], 1.08; 95% confidence interval [CI], 1.01‐1.19; P = .04) was associated with developing RN, although V12 Gy (OR, 1.03; 95% CI, 0.99‐1.06; P = .06), concurrent therapy (OR, 0.74; 95% CI, 0.17‐2.30; P = .76), prior WBRT, and ICI agents were not statistically significant. CONCLUSIONS Symptomatic RN occurs in a minority of patients with RCC brain metastases treated with ICI/SRS. The majority of events were grade 1 to 3 and were managed medically. Concurrent ICI/SRS does not appear to increase this risk. Attempts to improve dose conformality (reduce V12) may be the most successful mitigation strategy in single‐fraction SRS. The concurrent administration of immune checkpoint inhibitors and stereotactic radiosurgery in patients with renal cell carcinoma brain metastases is safe and well tolerated. Symptomatic radiation necrosis occurred in &lt;15% of patients, and all cases were managed medically.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.34087</identifier><identifier>PMID: 35077586</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Brain ; Brain cancer ; brain neoplasms ; carcinoma ; Chi-square test ; combined modality therapy ; Confidence intervals ; Immune checkpoint inhibitors ; Inhibitors ; Kidney cancer ; Metastases ; Metastasis ; Necrosis ; Oncology ; Radiation ; radiation injuries ; Radiation therapy ; Radiology ; Radiosurgery ; renal cell ; Renal cell carcinoma ; Statistical analysis ; Statistical tests ; Surgery ; Tumors</subject><ispartof>Cancer, 2022-04, Vol.128 (7), p.1429-1438</ispartof><rights>2022 American Cancer Society</rights><rights>2022 American Cancer Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3937-83d7d4804e806bf87dfeca1ef6d4c9d7b3cf51c610d118ad0cf2f07c7ad5cce53</citedby><cites>FETCH-LOGICAL-c3937-83d7d4804e806bf87dfeca1ef6d4c9d7b3cf51c610d118ad0cf2f07c7ad5cce53</cites><orcidid>0000-0002-9150-2916 ; 0000-0002-1216-6230</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35077586$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lehrer, Eric J.</creatorcontrib><creatorcontrib>Gurewitz, Jason</creatorcontrib><creatorcontrib>Bernstein, Kenneth</creatorcontrib><creatorcontrib>Patel, Dev</creatorcontrib><creatorcontrib>Kondziolka, Douglas</creatorcontrib><creatorcontrib>Niranjan, Ajay</creatorcontrib><creatorcontrib>Wei, Zhishuo</creatorcontrib><creatorcontrib>Lunsford, L. Dade</creatorcontrib><creatorcontrib>Malouff, Timothy D.</creatorcontrib><creatorcontrib>Ruiz‐Garcia, Henry</creatorcontrib><creatorcontrib>Patel, Samir</creatorcontrib><creatorcontrib>Bonney, Phillip A.</creatorcontrib><creatorcontrib>Hwang, Lindsay</creatorcontrib><creatorcontrib>Yu, Cheng</creatorcontrib><creatorcontrib>Zada, Gabriel</creatorcontrib><creatorcontrib>Mathieu, David</creatorcontrib><creatorcontrib>Trudel, Claire</creatorcontrib><creatorcontrib>Prasad, Rahul N.</creatorcontrib><creatorcontrib>Palmer, Joshua D.</creatorcontrib><creatorcontrib>Jones, Brianna M.</creatorcontrib><creatorcontrib>Sharma, Sonam</creatorcontrib><creatorcontrib>Fakhoury, Kareem R.</creatorcontrib><creatorcontrib>Rusthoven, Chad G.</creatorcontrib><creatorcontrib>Deibert, Christopher P.</creatorcontrib><creatorcontrib>Picozzi, Piero</creatorcontrib><creatorcontrib>Franzini, Andrea</creatorcontrib><creatorcontrib>Attuati, Luca</creatorcontrib><creatorcontrib>Lee, Cheng‐Chia</creatorcontrib><creatorcontrib>Yang, Huai‐Che</creatorcontrib><creatorcontrib>Ahluwalia, Manmeet S.</creatorcontrib><creatorcontrib>Sheehan, Jason P.</creatorcontrib><creatorcontrib>Trifiletti, Daniel M.</creatorcontrib><title>Radiation necrosis in renal cell carcinoma brain metastases treated with checkpoint inhibitors and radiosurgery: An international multicenter study</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND Patients with renal cell carcinoma (RCC) brain metastases are frequently treated with immune checkpoint inhibitors (ICIs) and stereotactic radiosurgery (SRS). However, data reporting on the risk of developing radiation necrosis (RN) are limited. METHODS RN rates were compared for concurrent therapy (ICI/SRS administration within 4 weeks of one another) and nonconcurrent therapy with the χ2 test. Univariable logistic regression was used to identify factors associated with developing RN. RESULTS Fifty patients (23 concurrent and 27 nonconcurrent) with 395 brain metastases were analyzed. The median follow‐up was 12.1 months; the median age was 65 years. The median margin dose was 20 Gy, and 4% underwent prior whole‐brain radiation therapy (WBRT). The median treated tumor volume was 3.32 cm3 (range, 0.06‐42.38 cm3); the median volume of normal brain tissue receiving a dose of 12 Gy or higher (V12 Gy) was 8.42 cm3 (range, 0.27‐111.22 cm3). Any‐grade RN occurred in 17.4% and 22.2% in the concurrent and nonconcurrent groups, respectively (P = .67). Symptomatic RN occurred in 4.3% and 14.8% in the concurrent and nonconcurrent groups, respectively (P = .23). Increased tumor volume during SRS (odds ratio [OR], 1.08; 95% confidence interval [CI], 1.01‐1.19; P = .04) was associated with developing RN, although V12 Gy (OR, 1.03; 95% CI, 0.99‐1.06; P = .06), concurrent therapy (OR, 0.74; 95% CI, 0.17‐2.30; P = .76), prior WBRT, and ICI agents were not statistically significant. CONCLUSIONS Symptomatic RN occurs in a minority of patients with RCC brain metastases treated with ICI/SRS. The majority of events were grade 1 to 3 and were managed medically. Concurrent ICI/SRS does not appear to increase this risk. Attempts to improve dose conformality (reduce V12) may be the most successful mitigation strategy in single‐fraction SRS. The concurrent administration of immune checkpoint inhibitors and stereotactic radiosurgery in patients with renal cell carcinoma brain metastases is safe and well tolerated. 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Dade</au><au>Malouff, Timothy D.</au><au>Ruiz‐Garcia, Henry</au><au>Patel, Samir</au><au>Bonney, Phillip A.</au><au>Hwang, Lindsay</au><au>Yu, Cheng</au><au>Zada, Gabriel</au><au>Mathieu, David</au><au>Trudel, Claire</au><au>Prasad, Rahul N.</au><au>Palmer, Joshua D.</au><au>Jones, Brianna M.</au><au>Sharma, Sonam</au><au>Fakhoury, Kareem R.</au><au>Rusthoven, Chad G.</au><au>Deibert, Christopher P.</au><au>Picozzi, Piero</au><au>Franzini, Andrea</au><au>Attuati, Luca</au><au>Lee, Cheng‐Chia</au><au>Yang, Huai‐Che</au><au>Ahluwalia, Manmeet S.</au><au>Sheehan, Jason P.</au><au>Trifiletti, Daniel M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiation necrosis in renal cell carcinoma brain metastases treated with checkpoint inhibitors and radiosurgery: An international multicenter study</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>128</volume><issue>7</issue><spage>1429</spage><epage>1438</epage><pages>1429-1438</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>BACKGROUND Patients with renal cell carcinoma (RCC) brain metastases are frequently treated with immune checkpoint inhibitors (ICIs) and stereotactic radiosurgery (SRS). However, data reporting on the risk of developing radiation necrosis (RN) are limited. METHODS RN rates were compared for concurrent therapy (ICI/SRS administration within 4 weeks of one another) and nonconcurrent therapy with the χ2 test. Univariable logistic regression was used to identify factors associated with developing RN. RESULTS Fifty patients (23 concurrent and 27 nonconcurrent) with 395 brain metastases were analyzed. The median follow‐up was 12.1 months; the median age was 65 years. The median margin dose was 20 Gy, and 4% underwent prior whole‐brain radiation therapy (WBRT). The median treated tumor volume was 3.32 cm3 (range, 0.06‐42.38 cm3); the median volume of normal brain tissue receiving a dose of 12 Gy or higher (V12 Gy) was 8.42 cm3 (range, 0.27‐111.22 cm3). Any‐grade RN occurred in 17.4% and 22.2% in the concurrent and nonconcurrent groups, respectively (P = .67). Symptomatic RN occurred in 4.3% and 14.8% in the concurrent and nonconcurrent groups, respectively (P = .23). Increased tumor volume during SRS (odds ratio [OR], 1.08; 95% confidence interval [CI], 1.01‐1.19; P = .04) was associated with developing RN, although V12 Gy (OR, 1.03; 95% CI, 0.99‐1.06; P = .06), concurrent therapy (OR, 0.74; 95% CI, 0.17‐2.30; P = .76), prior WBRT, and ICI agents were not statistically significant. CONCLUSIONS Symptomatic RN occurs in a minority of patients with RCC brain metastases treated with ICI/SRS. The majority of events were grade 1 to 3 and were managed medically. Concurrent ICI/SRS does not appear to increase this risk. Attempts to improve dose conformality (reduce V12) may be the most successful mitigation strategy in single‐fraction SRS. The concurrent administration of immune checkpoint inhibitors and stereotactic radiosurgery in patients with renal cell carcinoma brain metastases is safe and well tolerated. Symptomatic radiation necrosis occurred in &lt;15% of patients, and all cases were managed medically.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35077586</pmid><doi>10.1002/cncr.34087</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9150-2916</orcidid><orcidid>https://orcid.org/0000-0002-1216-6230</orcidid><oa>free_for_read</oa></addata></record>
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1097-0142
language eng
recordid cdi_proquest_miscellaneous_2622964453
source Wiley; EZB Free E-Journals
subjects Brain
Brain cancer
brain neoplasms
carcinoma
Chi-square test
combined modality therapy
Confidence intervals
Immune checkpoint inhibitors
Inhibitors
Kidney cancer
Metastases
Metastasis
Necrosis
Oncology
Radiation
radiation injuries
Radiation therapy
Radiology
Radiosurgery
renal cell
Renal cell carcinoma
Statistical analysis
Statistical tests
Surgery
Tumors
title Radiation necrosis in renal cell carcinoma brain metastases treated with checkpoint inhibitors and radiosurgery: An international multicenter study
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T04%3A39%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Radiation%20necrosis%20in%20renal%20cell%20carcinoma%20brain%20metastases%20treated%20with%20checkpoint%20inhibitors%20and%20radiosurgery:%20An%20international%20multicenter%20study&rft.jtitle=Cancer&rft.au=Lehrer,%20Eric%20J.&rft.date=2022-04-01&rft.volume=128&rft.issue=7&rft.spage=1429&rft.epage=1438&rft.pages=1429-1438&rft.issn=0008-543X&rft.eissn=1097-0142&rft_id=info:doi/10.1002/cncr.34087&rft_dat=%3Cproquest_cross%3E2622964453%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3937-83d7d4804e806bf87dfeca1ef6d4c9d7b3cf51c610d118ad0cf2f07c7ad5cce53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2637570453&rft_id=info:pmid/35077586&rfr_iscdi=true