<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wan G</submitter><funding>U.S. Department of Defense</funding><funding>U.S. Department of Defense (United States Department of Defense)</funding><funding>Dermatology Foundation</funding><funding>Dermatology Foundation (DF)</funding><funding>NIGMS NIH HHS</funding><pagination>79</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9622809</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(1)</volume><pubmed_abstract>Prognostic analysis for early-stage (stage I/II) melanomas is of paramount importance for customized surveillance and treatment plans. Since immune checkpoint inhibitors have recently been approved for stage IIB and IIC melanomas, prognostic tools to identify patients at high risk of recurrence have become even more critical. This study aims to assess the effectiveness of machine-learning algorithms in predicting melanoma recurrence using clinical and histopathologic features from Electronic Health Records (EHRs). We collected 1720 early-stage melanomas: 1172 from the Mass General Brigham healthcare system (MGB) and 548 from the Dana-Farber Cancer Institute (DFCI). We extracted 36 clinicopathologic features and used them to predict the recurrence risk with supervised machine-learning algor</pubmed_abstract><journal>NPJ precision oncology</journal><pubmed_title>Prediction of early-stage melanoma recurrence using clinical and histopathologic features.</pubmed_title><pmcid>PMC9622809</pmcid><funding_grant_id>R35 GM142879</funding_grant_id><funding_grant_id>W81XWH2110819</funding_grant_id><funding_grant_id>Medical Dermatology Career Development Award</funding_grant_id><pubmed_authors>Jiao M</pubmed_authors><pubmed_authors>Choi MS</pubmed_authors><pubmed_authors>Semenov YR</pubmed_authors><pubmed_authors>Boland GM</pubmed_authors><pubmed_authors>Marko-Varga G</pubmed_authors><pubmed_authors>Alexander NA</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Collier MR</pubmed_authors><pubmed_authors>Tang K</pubmed_authors><pubmed_authors>Valdes JG</pubmed_authors><pubmed_authors>Nemeth IB</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Jairath R</pubmed_authors><pubmed_authors>Yu KH</pubmed_authors><pubmed_authors>Phillipps JS</pubmed_authors><pubmed_authors>Wan G</pubmed_authors><pubmed_authors>Amadife M</pubmed_authors><pubmed_authors>Hua Y</pubmed_authors><pubmed_authors>Sorger PK</pubmed_authors><pubmed_authors>DeSimone MS</pubmed_authors><pubmed_authors>Nguyen N</pubmed_authors><pubmed_authors>Ho D</pubmed_authors><pubmed_authors>Duey S</pubmed_authors><pubmed_authors>Gusev A</pubmed_authors><pubmed_authors>Leung BW</pubmed_authors><pubmed_authors>Rajeh A</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Liu F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prediction of early-stage melanoma recurrence using clinical and histopathologic features.</name><description>Prognostic analysis for early-stage (stage I/II) melanomas is of paramount importance for customized surveillance and treatment plans. Since immune checkpoint inhibitors have recently been approved for stage IIB and IIC melanomas, prognostic tools to identify patients at high risk of recurrence have become even more critical. This study aims to assess the effectiveness of machine-learning algorithms in predicting melanoma recurrence using clinical and histopathologic features from Electronic Health Records (EHRs). We collected 1720 early-stage melanomas: 1172 from the Mass General Brigham healthcare system (MGB) and 548 from the Dana-Farber Cancer Institute (DFCI). We extracted 36 clinicopathologic features and used them to predict the recurrence risk with supervised machine-learning algor</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-03T10:52:47.047Z</modification><creation>2025-04-07T13:01:57.354Z</creation></dates><accession>S-EPMC9622809</accession><cross_references><pubmed>36316482</pubmed><doi>10.1038/s41698-022-00321-4</doi></cross_references></HashMap>