Frailty and checkpoint inhibitor toxicity in older patients with melanoma

Background Immune checkpoint inhibitors (ICIs) can cause immune‐related adverse events (irAEs) that range from mild to life‐threatening. Age itself does not seem to be a predictor for the occurrence of irAEs. It is unknown whether frailty plays a role in the occurrence of irAEs. Therefore, the autho...

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Veröffentlicht in:Cancer 2022-07, Vol.128 (14), p.2746-2752
Hauptverfasser: Bruijnen, Cheryl P., Koldenhof, José J., Verheijden, Rik J., Bos, Frederiek, Emmelot‐Vonk, Mariëlle H., Witteveen, Petronella O., Suijkerbuijk, Karijn P. M.
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container_end_page 2752
container_issue 14
container_start_page 2746
container_title Cancer
container_volume 128
creator Bruijnen, Cheryl P.
Koldenhof, José J.
Verheijden, Rik J.
Bos, Frederiek
Emmelot‐Vonk, Mariëlle H.
Witteveen, Petronella O.
Suijkerbuijk, Karijn P. M.
description Background Immune checkpoint inhibitors (ICIs) can cause immune‐related adverse events (irAEs) that range from mild to life‐threatening. Age itself does not seem to be a predictor for the occurrence of irAEs. It is unknown whether frailty plays a role in the occurrence of irAEs. Therefore, the authors assessed whether irAEs and their sequelae occur more often in frail patients than in fit patients according to the Geriatric 8 (G8) assessment. Methods Patients with melanoma aged 70 years and older who were about to start ICI therapy and were screened with the G8 assessment were enrolled in this prospective, observational study. Patients were classified by the G8 as either fit or frail. The primary outcome was the occurrence of grade ≥3 irAEs. Results In total, 92 patients were included for statistical analyses, 26 (29%) of whom were classified as frail. Grade ≥3 irAEs occurred in 20% of patients. There was no significant difference in the occurrence of grade ≥3 irAEs between fit and frail patients (17% vs 27%; P = .26). Frail patients were admitted to the hospital because of irAEs significantly more often than fit patients (29% vs 54%; P = .02) and showed a trend toward increased length of hospitalization (5 vs 8 days; P = .06) and more frequent use of immunosuppressants or ICI discontinuation for irAEs (36% vs 58%; P = .06). Conclusions Although frailty appears to be unrelated to the occurrence of severe irAEs, it is an indicator of irAE‐related adverse sequelae, such as hospital admission. Screening for frailty can be of added value in the shared decision‐making process for older patients who qualify for ICI treatment. Frailty screening with the Geriatric 8 (G8) was used as a guide for making individualized treatment decisions. Frailty according to the G8 was associated with sequelae of immune‐related adverse events, such as hospitalizations and visits to the emergency department.
doi_str_mv 10.1002/cncr.34230
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M.</creator><creatorcontrib>Bruijnen, Cheryl P. ; Koldenhof, José J. ; Verheijden, Rik J. ; Bos, Frederiek ; Emmelot‐Vonk, Mariëlle H. ; Witteveen, Petronella O. ; Suijkerbuijk, Karijn P. M.</creatorcontrib><description>Background Immune checkpoint inhibitors (ICIs) can cause immune‐related adverse events (irAEs) that range from mild to life‐threatening. Age itself does not seem to be a predictor for the occurrence of irAEs. It is unknown whether frailty plays a role in the occurrence of irAEs. Therefore, the authors assessed whether irAEs and their sequelae occur more often in frail patients than in fit patients according to the Geriatric 8 (G8) assessment. Methods Patients with melanoma aged 70 years and older who were about to start ICI therapy and were screened with the G8 assessment were enrolled in this prospective, observational study. Patients were classified by the G8 as either fit or frail. The primary outcome was the occurrence of grade ≥3 irAEs. Results In total, 92 patients were included for statistical analyses, 26 (29%) of whom were classified as frail. Grade ≥3 irAEs occurred in 20% of patients. There was no significant difference in the occurrence of grade ≥3 irAEs between fit and frail patients (17% vs 27%; P = .26). Frail patients were admitted to the hospital because of irAEs significantly more often than fit patients (29% vs 54%; P = .02) and showed a trend toward increased length of hospitalization (5 vs 8 days; P = .06) and more frequent use of immunosuppressants or ICI discontinuation for irAEs (36% vs 58%; P = .06). Conclusions Although frailty appears to be unrelated to the occurrence of severe irAEs, it is an indicator of irAE‐related adverse sequelae, such as hospital admission. Screening for frailty can be of added value in the shared decision‐making process for older patients who qualify for ICI treatment. Frailty screening with the Geriatric 8 (G8) was used as a guide for making individualized treatment decisions. Frailty according to the G8 was associated with sequelae of immune‐related adverse events, such as hospitalizations and visits to the emergency department.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.34230</identifier><identifier>PMID: 35439334</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Complications ; Decision making ; Frailty ; Geriatric 8 ; Immune checkpoint inhibitors ; immune‐related adverse events ; Immunosuppressive agents ; Melanoma ; Oncology ; Original ; Patients ; Quality ; Statistical analysis ; Toxicity</subject><ispartof>Cancer, 2022-07, Vol.128 (14), p.2746-2752</ispartof><rights>2022 The Authors. published by Wiley Periodicals LLC on behalf of American Cancer Society</rights><rights>2022 The Authors. 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M.</creatorcontrib><title>Frailty and checkpoint inhibitor toxicity in older patients with melanoma</title><title>Cancer</title><addtitle>Cancer</addtitle><description>Background Immune checkpoint inhibitors (ICIs) can cause immune‐related adverse events (irAEs) that range from mild to life‐threatening. Age itself does not seem to be a predictor for the occurrence of irAEs. It is unknown whether frailty plays a role in the occurrence of irAEs. Therefore, the authors assessed whether irAEs and their sequelae occur more often in frail patients than in fit patients according to the Geriatric 8 (G8) assessment. Methods Patients with melanoma aged 70 years and older who were about to start ICI therapy and were screened with the G8 assessment were enrolled in this prospective, observational study. Patients were classified by the G8 as either fit or frail. The primary outcome was the occurrence of grade ≥3 irAEs. Results In total, 92 patients were included for statistical analyses, 26 (29%) of whom were classified as frail. Grade ≥3 irAEs occurred in 20% of patients. There was no significant difference in the occurrence of grade ≥3 irAEs between fit and frail patients (17% vs 27%; P = .26). Frail patients were admitted to the hospital because of irAEs significantly more often than fit patients (29% vs 54%; P = .02) and showed a trend toward increased length of hospitalization (5 vs 8 days; P = .06) and more frequent use of immunosuppressants or ICI discontinuation for irAEs (36% vs 58%; P = .06). Conclusions Although frailty appears to be unrelated to the occurrence of severe irAEs, it is an indicator of irAE‐related adverse sequelae, such as hospital admission. Screening for frailty can be of added value in the shared decision‐making process for older patients who qualify for ICI treatment. Frailty screening with the Geriatric 8 (G8) was used as a guide for making individualized treatment decisions. 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M.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bruijnen, Cheryl P.</au><au>Koldenhof, José J.</au><au>Verheijden, Rik J.</au><au>Bos, Frederiek</au><au>Emmelot‐Vonk, Mariëlle H.</au><au>Witteveen, Petronella O.</au><au>Suijkerbuijk, Karijn P. M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frailty and checkpoint inhibitor toxicity in older patients with melanoma</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2022-07-15</date><risdate>2022</risdate><volume>128</volume><issue>14</issue><spage>2746</spage><epage>2752</epage><pages>2746-2752</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>Background Immune checkpoint inhibitors (ICIs) can cause immune‐related adverse events (irAEs) that range from mild to life‐threatening. Age itself does not seem to be a predictor for the occurrence of irAEs. It is unknown whether frailty plays a role in the occurrence of irAEs. Therefore, the authors assessed whether irAEs and their sequelae occur more often in frail patients than in fit patients according to the Geriatric 8 (G8) assessment. Methods Patients with melanoma aged 70 years and older who were about to start ICI therapy and were screened with the G8 assessment were enrolled in this prospective, observational study. Patients were classified by the G8 as either fit or frail. The primary outcome was the occurrence of grade ≥3 irAEs. Results In total, 92 patients were included for statistical analyses, 26 (29%) of whom were classified as frail. Grade ≥3 irAEs occurred in 20% of patients. There was no significant difference in the occurrence of grade ≥3 irAEs between fit and frail patients (17% vs 27%; P = .26). Frail patients were admitted to the hospital because of irAEs significantly more often than fit patients (29% vs 54%; P = .02) and showed a trend toward increased length of hospitalization (5 vs 8 days; P = .06) and more frequent use of immunosuppressants or ICI discontinuation for irAEs (36% vs 58%; P = .06). Conclusions Although frailty appears to be unrelated to the occurrence of severe irAEs, it is an indicator of irAE‐related adverse sequelae, such as hospital admission. Screening for frailty can be of added value in the shared decision‐making process for older patients who qualify for ICI treatment. Frailty screening with the Geriatric 8 (G8) was used as a guide for making individualized treatment decisions. Frailty according to the G8 was associated with sequelae of immune‐related adverse events, such as hospitalizations and visits to the emergency department.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>35439334</pmid><doi>10.1002/cncr.34230</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-1629-3421</orcidid><orcidid>https://orcid.org/0000-0003-4205-6611</orcidid><oa>free_for_read</oa></addata></record>
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subjects Complications
Decision making
Frailty
Geriatric 8
Immune checkpoint inhibitors
immune‐related adverse events
Immunosuppressive agents
Melanoma
Oncology
Original
Patients
Quality
Statistical analysis
Toxicity
title Frailty and checkpoint inhibitor toxicity in older patients with melanoma
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