<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Anderson EC</submitter><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Center for Advancing Translational Sciences</funding><funding>NCATS NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Cancer Institute</funding><funding>Harold Alfond Foundation</funding><funding>NCI NIH HHS</funding><pagination>67</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10924947</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>Genomic tumor testing (GTT) is an emerging technology aimed at identifying variants in tumors that can be targeted with genomically matched drugs. Due to limited resources, rural patients receiving care in community oncology settings may be less likely to benefit from GTT. We analyzed GTT results and observational clinical outcomes data from patients enrolled in the Maine Cancer Genomics Initiative (MCGI), which provided access to GTTs; clinician educational resources; and genomic tumor boards in community practices in a predominantly rural state. 1603 adult cancer patients completed enrollment; 1258 had at least one potentially actionable variant identified. 206 (16.4%) patients received a total of 240 genome matched treatments, of those treatments, 64% were FDA-approved in the tumor type</pubmed_abstract><journal>NPJ precision oncology</journal><pubmed_title>Genome-matched treatments and patient outcomes in the Maine Cancer Genomics Initiative (MCGI).</pubmed_title><pmcid>PMC10924947</pmcid><funding_grant_id>KL2TR002545</funding_grant_id><funding_grant_id>P30 CA034196</funding_grant_id><funding_grant_id>KL2 TR002545</funding_grant_id><pubmed_authors>Han PKJ</pubmed_authors><pubmed_authors>DiPalazzo J</pubmed_authors><pubmed_authors>Brooks PL</pubmed_authors><pubmed_authors>Gaitor L</pubmed_authors><pubmed_authors>Bourne J</pubmed_authors><pubmed_authors>Helbig P</pubmed_authors><pubmed_authors>Sinclair SJ</pubmed_authors><pubmed_authors>Rueter J</pubmed_authors><pubmed_authors>Graham L</pubmed_authors><pubmed_authors>Rasmussen K</pubmed_authors><pubmed_authors>Hall MJ</pubmed_authors><pubmed_authors>Antov A</pubmed_authors><pubmed_authors>Bradford LS</pubmed_authors><pubmed_authors>Anderson EC</pubmed_authors><pubmed_authors>Thomas CA</pubmed_authors><pubmed_authors>Inhorn R</pubmed_authors><pubmed_authors>Lucas FL</pubmed_authors><pubmed_authors>Lu-Emerson C</pubmed_authors><pubmed_authors>Liu ET</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genome-matched treatments and patient outcomes in the Maine Cancer Genomics Initiative (MCGI).</name><description>Genomic tumor testing (GTT) is an emerging technology aimed at identifying variants in tumors that can be targeted with genomically matched drugs. Due to limited resources, rural patients receiving care in community oncology settings may be less likely to benefit from GTT. We analyzed GTT results and observational clinical outcomes data from patients enrolled in the Maine Cancer Genomics Initiative (MCGI), which provided access to GTTs; clinician educational resources; and genomic tumor boards in community practices in a predominantly rural state. 1603 adult cancer patients completed enrollment; 1258 had at least one potentially actionable variant identified. 206 (16.4%) patients received a total of 240 genome matched treatments, of those treatments, 64% were FDA-approved in the tumor type</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-04T12:58:39.898Z</modification><creation>2025-04-04T12:58:39.898Z</creation></dates><accession>S-EPMC10924947</accession><cross_references><pubmed>38461318</pubmed><doi>10.1038/s41698-024-00547-4</doi></cross_references></HashMap>