<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Seethapathy H</submitter><funding>Claflin Distinguished Scholars Award</funding><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><pagination>507-514</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8875461</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>37(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Our objective was to characterize the incidence, risk factors and clinical features of acute kidney injury (AKI) in patients receiving dabrafenib and trametinib.&lt;h4>Methods&lt;/h4>We performed a retrospective cohort study examining the kidney outcomes of patients in a large healthcare system who received dabrafenib/trametinib between 2010 and 2019. The primary outcome was AKI, defined as a 1.5-fold increase in serum creatinine from baseline within a 12-month study period. AKI severity and etiology was determined for each case by chart review. Logistic regression was used to evaluate baseline predictors of AKI.&lt;h4>Results&lt;/h4>A total of 199 patients who received dabrafenib in our healthcare system from 2010 to 2019 were included in the analysis. Forty-two patients (21%) expe</pubmed_abstract><journal>Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association</journal><pubmed_title>Clinical features of acute kidney injury in patients receiving dabrafenib and trametinib.</pubmed_title><pmcid>PMC8875461</pmcid><funding_grant_id>K23 DK117014</funding_grant_id><funding_grant_id>K23 DK 117014</funding_grant_id><funding_grant_id>NIH</funding_grant_id><pubmed_authors>Reynolds KL</pubmed_authors><pubmed_authors>Lee MD</pubmed_authors><pubmed_authors>Sise ME</pubmed_authors><pubmed_authors>Seethapathy H</pubmed_authors><pubmed_authors>Fadden RM</pubmed_authors><pubmed_authors>Rosales IA</pubmed_authors><pubmed_authors>Efe O</pubmed_authors><pubmed_authors>Chute DF</pubmed_authors><pubmed_authors>Kaufman HL</pubmed_authors><pubmed_authors>Colvin RB</pubmed_authors><pubmed_authors>Strohbehn IA</pubmed_authors><pubmed_authors>Jhaveri KD</pubmed_authors><pubmed_authors>Sullivan RJ</pubmed_authors><pubmed_authors>Rusibamayila N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clinical features of acute kidney injury in patients receiving dabrafenib and trametinib.</name><description>&lt;h4>Background&lt;/h4>Our objective was to characterize the incidence, risk factors and clinical features of acute kidney injury (AKI) in patients receiving dabrafenib and trametinib.&lt;h4>Methods&lt;/h4>We performed a retrospective cohort study examining the kidney outcomes of patients in a large healthcare system who received dabrafenib/trametinib between 2010 and 2019. The primary outcome was AKI, defined as a 1.5-fold increase in serum creatinine from baseline within a 12-month study period. AKI severity and etiology was determined for each case by chart review. Logistic regression was used to evaluate baseline predictors of AKI.&lt;h4>Results&lt;/h4>A total of 199 patients who received dabrafenib in our healthcare system from 2010 to 2019 were included in the analysis. Forty-two patients (21%) expe</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2026-03-27T16:43:21.944Z</modification><creation>2025-04-04T08:57:40.433Z</creation></dates><accession>S-EPMC8875461</accession><cross_references><pubmed>33355659</pubmed><doi>10.1093/ndt/gfaa372</doi></cross_references></HashMap>