Acute kidney injury in patients treated with anti-programmed death receptor-1 for advanced melanoma: a real-life study in a single-centre cohort

Abstract Background Immune checkpoints inhibitors have transformed the prognosis of advanced melanoma but are associated with immune-related adverse events (irAEs). We evaluated the incidence, risk factors and causes of acute kidney injury (AKI) in a monocentric real-life cohort of patients treated...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2021-08, Vol.36 (9), p.1664-1674
Hauptverfasser: Stein, Claire, Burtey, Stéphane, Mancini, Julien, Pelletier, Marion, Sallée, Marion, Brunet, Philippe, Berbis, Philippe, Grob, Jean Jacques, Honoré, Stéphane, Gaudy, Caroline, Jourde-Chiche, Noémie
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container_end_page 1674
container_issue 9
container_start_page 1664
container_title Nephrology, dialysis, transplantation
container_volume 36
creator Stein, Claire
Burtey, Stéphane
Mancini, Julien
Pelletier, Marion
Sallée, Marion
Brunet, Philippe
Berbis, Philippe
Grob, Jean Jacques
Honoré, Stéphane
Gaudy, Caroline
Jourde-Chiche, Noémie
description Abstract Background Immune checkpoints inhibitors have transformed the prognosis of advanced melanoma but are associated with immune-related adverse events (irAEs). We evaluated the incidence, risk factors and causes of acute kidney injury (AKI) in a monocentric real-life cohort of patients treated with anti-programmed death receptor-1 (anti-PD1) antibodies for advanced melanoma. Methods Retrospective collection of medical charts and comprehensive analysis of lab results from patients treated with nivolumab or pembrolizumab for advanced melanoma between 2014 and 2018 was carried out. AKI was defined by Kidney Disease Improving Global Outcomes criteria, and causes were determined by chart review. Overall survival, survival without AKI and impact of AKI on survival were analysed. Risk factors for death and for AKI were identified. Results Two hundred and thirty-nine patients were included. Forty-one (17%) had at least one episode of AKI. Independent risk factors for AKI were treatment with renin–angiotensin–aldosterone system inhibitors (RAASi), pre-existing chronic kidney disease (CKD) and cumulated doses of anti-PD1. The main cause of AKI was prerenal, and only eight patients (3.3%) developed acute interstitial nephritis; 8% of patients developed CKD. The median overall survival was 13.4 months and was not affected by AKI. In multivariate analysis, the overall mortality was lower in overweight and obese patients and higher in patients treated with proton-pump inhibitors (PPI) or corticosteroids. Conclusions AKI is common in patients treated with anti-PD1 for advanced melanoma but is mostly prerenal and favoured by the use of RAASi; renal irAE is rare. PPI and corticosteroids were associated with poor survival in this population, while overweight/obesity was protective. GRAPHICAL ABSTRACT
doi_str_mv 10.1093/ndt/gfaa137
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We evaluated the incidence, risk factors and causes of acute kidney injury (AKI) in a monocentric real-life cohort of patients treated with anti-programmed death receptor-1 (anti-PD1) antibodies for advanced melanoma. Methods Retrospective collection of medical charts and comprehensive analysis of lab results from patients treated with nivolumab or pembrolizumab for advanced melanoma between 2014 and 2018 was carried out. AKI was defined by Kidney Disease Improving Global Outcomes criteria, and causes were determined by chart review. Overall survival, survival without AKI and impact of AKI on survival were analysed. Risk factors for death and for AKI were identified. Results Two hundred and thirty-nine patients were included. Forty-one (17%) had at least one episode of AKI. Independent risk factors for AKI were treatment with renin–angiotensin–aldosterone system inhibitors (RAASi), pre-existing chronic kidney disease (CKD) and cumulated doses of anti-PD1. The main cause of AKI was prerenal, and only eight patients (3.3%) developed acute interstitial nephritis; 8% of patients developed CKD. The median overall survival was 13.4 months and was not affected by AKI. In multivariate analysis, the overall mortality was lower in overweight and obese patients and higher in patients treated with proton-pump inhibitors (PPI) or corticosteroids. Conclusions AKI is common in patients treated with anti-PD1 for advanced melanoma but is mostly prerenal and favoured by the use of RAASi; renal irAE is rare. PPI and corticosteroids were associated with poor survival in this population, while overweight/obesity was protective. 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All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c357t-4659dc02b4540c1afbbf7e2485a79aadfc20010ca2833191e2e5e2cb8645ee4d3</citedby><cites>FETCH-LOGICAL-c357t-4659dc02b4540c1afbbf7e2485a79aadfc20010ca2833191e2e5e2cb8645ee4d3</cites><orcidid>0000-0001-9315-1577 ; 0000-0001-9500-8598</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32941608$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://inserm.hal.science/inserm-03106263$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Stein, Claire</creatorcontrib><creatorcontrib>Burtey, Stéphane</creatorcontrib><creatorcontrib>Mancini, Julien</creatorcontrib><creatorcontrib>Pelletier, Marion</creatorcontrib><creatorcontrib>Sallée, Marion</creatorcontrib><creatorcontrib>Brunet, Philippe</creatorcontrib><creatorcontrib>Berbis, Philippe</creatorcontrib><creatorcontrib>Grob, Jean Jacques</creatorcontrib><creatorcontrib>Honoré, Stéphane</creatorcontrib><creatorcontrib>Gaudy, Caroline</creatorcontrib><creatorcontrib>Jourde-Chiche, Noémie</creatorcontrib><title>Acute kidney injury in patients treated with anti-programmed death receptor-1 for advanced melanoma: a real-life study in a single-centre cohort</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Abstract Background Immune checkpoints inhibitors have transformed the prognosis of advanced melanoma but are associated with immune-related adverse events (irAEs). We evaluated the incidence, risk factors and causes of acute kidney injury (AKI) in a monocentric real-life cohort of patients treated with anti-programmed death receptor-1 (anti-PD1) antibodies for advanced melanoma. Methods Retrospective collection of medical charts and comprehensive analysis of lab results from patients treated with nivolumab or pembrolizumab for advanced melanoma between 2014 and 2018 was carried out. AKI was defined by Kidney Disease Improving Global Outcomes criteria, and causes were determined by chart review. Overall survival, survival without AKI and impact of AKI on survival were analysed. Risk factors for death and for AKI were identified. Results Two hundred and thirty-nine patients were included. Forty-one (17%) had at least one episode of AKI. Independent risk factors for AKI were treatment with renin–angiotensin–aldosterone system inhibitors (RAASi), pre-existing chronic kidney disease (CKD) and cumulated doses of anti-PD1. The main cause of AKI was prerenal, and only eight patients (3.3%) developed acute interstitial nephritis; 8% of patients developed CKD. The median overall survival was 13.4 months and was not affected by AKI. In multivariate analysis, the overall mortality was lower in overweight and obese patients and higher in patients treated with proton-pump inhibitors (PPI) or corticosteroids. Conclusions AKI is common in patients treated with anti-PD1 for advanced melanoma but is mostly prerenal and favoured by the use of RAASi; renal irAE is rare. PPI and corticosteroids were associated with poor survival in this population, while overweight/obesity was protective. GRAPHICAL ABSTRACT</description><subject>Acute Kidney Injury - chemically induced</subject><subject>Antibodies, Monoclonal, Humanized - adverse effects</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Melanoma - drug therapy</subject><subject>Nivolumab - adverse effects</subject><subject>Receptors, Death Domain - antagonists &amp; inhibitors</subject><subject>Retrospective Studies</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v1DAQxS0EotvCiTvyCSFBqP8lTritKkqRVuICZ2viTHZdEjvYTlG_BR8Zl1165PSkeT-90cwj5BVnHzjr5KUf8uV-BOBSPyEbrhpWCdnWT8mmuLxiNevOyHlKt4yxTmj9nJxJ0SnesHZDfm_tmpH-cIPHe-r87RofhC6QHfqcaI4IGQf6y-UDBZ9dtcSwjzDPZTgU70AjWlxyiBWnY4gUhjvwtrgzTuDDDB8pFAamanIj0pTX4e8KoMn5_YSVLYsiUhsOIeYX5NkIU8KXJ70g368_fbu6qXZfP3-52u4qK2udK9XU3WCZ6FWtmOUw9v2oUai2Bt0BDKMVjHFmQbRS8o6jwBqF7dtG1YhqkBfk_TH3AJNZopsh3psAztxsd8b5hHE2THLWiEbe8YK_PeLl-p8rpmxmlyxO5UIMazJCKSW11g0r6LsjamNIKeL4GM-ZeWjMlMbMqbFCvz4Fr3156SP7r6ICvDkCYV3-m_QHdTKhUQ</recordid><startdate>20210827</startdate><enddate>20210827</enddate><creator>Stein, Claire</creator><creator>Burtey, Stéphane</creator><creator>Mancini, Julien</creator><creator>Pelletier, Marion</creator><creator>Sallée, Marion</creator><creator>Brunet, Philippe</creator><creator>Berbis, Philippe</creator><creator>Grob, Jean Jacques</creator><creator>Honoré, Stéphane</creator><creator>Gaudy, Caroline</creator><creator>Jourde-Chiche, Noémie</creator><general>Oxford University Press</general><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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-9315-1577</orcidid><orcidid>https://orcid.org/0000-0001-9500-8598</orcidid></search><sort><creationdate>20210827</creationdate><title>Acute kidney injury in patients treated with anti-programmed death receptor-1 for advanced melanoma: a real-life study in a single-centre cohort</title><author>Stein, Claire ; Burtey, Stéphane ; Mancini, Julien ; Pelletier, Marion ; Sallée, Marion ; Brunet, Philippe ; Berbis, Philippe ; Grob, Jean Jacques ; Honoré, Stéphane ; Gaudy, Caroline ; Jourde-Chiche, Noémie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-4659dc02b4540c1afbbf7e2485a79aadfc20010ca2833191e2e5e2cb8645ee4d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute Kidney Injury - chemically induced</topic><topic>Antibodies, Monoclonal, Humanized - adverse effects</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Melanoma - drug therapy</topic><topic>Nivolumab - adverse effects</topic><topic>Receptors, Death Domain - antagonists &amp; inhibitors</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stein, Claire</creatorcontrib><creatorcontrib>Burtey, Stéphane</creatorcontrib><creatorcontrib>Mancini, Julien</creatorcontrib><creatorcontrib>Pelletier, Marion</creatorcontrib><creatorcontrib>Sallée, Marion</creatorcontrib><creatorcontrib>Brunet, Philippe</creatorcontrib><creatorcontrib>Berbis, Philippe</creatorcontrib><creatorcontrib>Grob, Jean Jacques</creatorcontrib><creatorcontrib>Honoré, Stéphane</creatorcontrib><creatorcontrib>Gaudy, Caroline</creatorcontrib><creatorcontrib>Jourde-Chiche, Noémie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stein, Claire</au><au>Burtey, Stéphane</au><au>Mancini, Julien</au><au>Pelletier, Marion</au><au>Sallée, Marion</au><au>Brunet, Philippe</au><au>Berbis, Philippe</au><au>Grob, Jean Jacques</au><au>Honoré, Stéphane</au><au>Gaudy, Caroline</au><au>Jourde-Chiche, Noémie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute kidney injury in patients treated with anti-programmed death receptor-1 for advanced melanoma: a real-life study in a single-centre cohort</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2021-08-27</date><risdate>2021</risdate><volume>36</volume><issue>9</issue><spage>1664</spage><epage>1674</epage><pages>1664-1674</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><abstract>Abstract Background Immune checkpoints inhibitors have transformed the prognosis of advanced melanoma but are associated with immune-related adverse events (irAEs). We evaluated the incidence, risk factors and causes of acute kidney injury (AKI) in a monocentric real-life cohort of patients treated with anti-programmed death receptor-1 (anti-PD1) antibodies for advanced melanoma. Methods Retrospective collection of medical charts and comprehensive analysis of lab results from patients treated with nivolumab or pembrolizumab for advanced melanoma between 2014 and 2018 was carried out. AKI was defined by Kidney Disease Improving Global Outcomes criteria, and causes were determined by chart review. Overall survival, survival without AKI and impact of AKI on survival were analysed. Risk factors for death and for AKI were identified. Results Two hundred and thirty-nine patients were included. Forty-one (17%) had at least one episode of AKI. Independent risk factors for AKI were treatment with renin–angiotensin–aldosterone system inhibitors (RAASi), pre-existing chronic kidney disease (CKD) and cumulated doses of anti-PD1. The main cause of AKI was prerenal, and only eight patients (3.3%) developed acute interstitial nephritis; 8% of patients developed CKD. The median overall survival was 13.4 months and was not affected by AKI. In multivariate analysis, the overall mortality was lower in overweight and obese patients and higher in patients treated with proton-pump inhibitors (PPI) or corticosteroids. Conclusions AKI is common in patients treated with anti-PD1 for advanced melanoma but is mostly prerenal and favoured by the use of RAASi; renal irAE is rare. PPI and corticosteroids were associated with poor survival in this population, while overweight/obesity was protective. GRAPHICAL ABSTRACT</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32941608</pmid><doi>10.1093/ndt/gfaa137</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9315-1577</orcidid><orcidid>https://orcid.org/0000-0001-9500-8598</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Acute Kidney Injury - chemically induced
Antibodies, Monoclonal, Humanized - adverse effects
Humans
Life Sciences
Melanoma - drug therapy
Nivolumab - adverse effects
Receptors, Death Domain - antagonists & inhibitors
Retrospective Studies
title Acute kidney injury in patients treated with anti-programmed death receptor-1 for advanced melanoma: a real-life study in a single-centre cohort
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