<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cortazar FB</submitter><funding>American Society of Nephrology</funding><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>ASN</funding><funding>NIDDK</funding><pagination>435-446</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7003302</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>31(2)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Despite increasing recognition of the importance of immune checkpoint inhibitor-associated AKI, data on this complication of immunotherapy are sparse.&lt;h4>Methods&lt;/h4>We conducted a multicenter study of 138 patients with immune checkpoint inhibitor-associated AKI, defined as a ≥2-fold increase in serum creatinine or new dialysis requirement directly attributed to an immune checkpoint inhibitor. We also collected data on 276 control patients who received these drugs but did not develop AKI.&lt;h4>Results&lt;/h4>Lower baseline eGFR, proton pump inhibitor use, and combination immune checkpoint inhibitor therapy were each independently associated with an increased risk of immune checkpoint inhibitor-associated AKI. Median (interquartile range) time from immune checkpoint inhibitor </pubmed_abstract><journal>Journal of the American Society of Nephrology : JASN</journal><pubmed_title>Clinical Features and Outcomes of Immune Checkpoint Inhibitor-Associated AKI: A Multicenter Study.</pubmed_title><pmcid>PMC7003302</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>K23 DK117014</funding_grant_id><funding_grant_id>K23DK117014</funding_grant_id><funding_grant_id>K23DK106448</funding_grant_id><funding_grant_id>K08DK120868</funding_grant_id><funding_grant_id>R01 HL144566</funding_grant_id><funding_grant_id>K08 DK118120</funding_grant_id><funding_grant_id>P30CA008748</funding_grant_id><funding_grant_id>K23 DK106448</funding_grant_id><funding_grant_id>K08DK118120</funding_grant_id><funding_grant_id>R01HL144566</funding_grant_id><funding_grant_id>K08 DK120868</funding_grant_id><funding_grant_id>T32 DK007219</funding_grant_id><pubmed_authors>Dinh AR</pubmed_authors><pubmed_authors>Shin DS</pubmed_authors><pubmed_authors>Reynolds KL</pubmed_authors><pubmed_authors>Ortiz-Melo DI</pubmed_authors><pubmed_authors>Rangarajan S</pubmed_authors><pubmed_authors>Hogan JJ</pubmed_authors><pubmed_authors>Mamlouk O</pubmed_authors><pubmed_authors>Cortazar FB</pubmed_authors><pubmed_authors>Abudayyeh A</pubmed_authors><pubmed_authors>Manohar S</pubmed_authors><pubmed_authors>Kitchlu A</pubmed_authors><pubmed_authors>Murakami N</pubmed_authors><pubmed_authors>Assal A</pubmed_authors><pubmed_authors>Uprety D</pubmed_authors><pubmed_authors>Leaf DE</pubmed_authors><pubmed_authors>Malik AB</pubmed_authors><pubmed_authors>Mithani Z</pubmed_authors><pubmed_authors>Gupta S</pubmed_authors><pubmed_authors>Shirali AC</pubmed_authors><pubmed_authors>Sharma S</pubmed_authors><pubmed_authors>Sise ME</pubmed_authors><pubmed_authors>Shirazian S</pubmed_authors><pubmed_authors>Kibbelaar ZA</pubmed_authors><pubmed_authors>Johnson DB</pubmed_authors><pubmed_authors>Herrmann SM</pubmed_authors><pubmed_authors>Marrone KA</pubmed_authors><pubmed_authors>Glezerman IG</pubmed_authors><pubmed_authors>Vijayan A</pubmed_authors><pubmed_authors>Renaghan AD</pubmed_authors><pubmed_authors>Hosseini A</pubmed_authors><pubmed_authors>Motwani SS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical Features and Outcomes of Immune Checkpoint Inhibitor-Associated AKI: A Multicenter Study.</name><description>&lt;h4>Background&lt;/h4>Despite increasing recognition of the importance of immune checkpoint inhibitor-associated AKI, data on this complication of immunotherapy are sparse.&lt;h4>Methods&lt;/h4>We conducted a multicenter study of 138 patients with immune checkpoint inhibitor-associated AKI, defined as a ≥2-fold increase in serum creatinine or new dialysis requirement directly attributed to an immune checkpoint inhibitor. We also collected data on 276 control patients who received these drugs but did not develop AKI.&lt;h4>Results&lt;/h4>Lower baseline eGFR, proton pump inhibitor use, and combination immune checkpoint inhibitor therapy were each independently associated with an increased risk of immune checkpoint inhibitor-associated AKI. Median (interquartile range) time from immune checkpoint inhibitor </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2025-04-26T18:50:40.897Z</modification><creation>2021-02-21T04:29:27Z</creation></dates><accession>S-EPMC7003302</accession><cross_references><pubmed>31896554</pubmed><doi>10.1681/ASN.2019070676</doi><doi>10.1681/asn.2019070676</doi></cross_references></HashMap>