<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(18)</volume><submitter>Shimizu H</submitter><pubmed_abstract>&lt;b>Background&lt;/b>: Blood-based comprehensive genomic profiling (CGP), a form of liquid biopsy, is often used for biliary tract cancer (BTC) when tissue-based CGP (tissue CGP) is unavailable, despite lower detection rates. This study explored factors linked to detecting actionable genomic alterations to optimize its use. &lt;b>Methods&lt;/b>: We retrospectively analyzed BTC cases in Japan's C-CAT (June 2019-January 2025), restricting panel comparisons to FoundationOne&lt;sup>®&lt;/sup> CDx (F1; n = 5019) and FoundationOne&lt;sup>®&lt;/sup> Liquid CDx (F1L; n = 1550). Missing covariates were handled by multiple imputations (m = 20). Between-panel balance used 1:1 propensity-score matching (caliper 0.2). Outcomes were modeled with logistic regression. Targets included MSI-H, TMB-H, &lt;i>FGFR2&lt;/i>/&lt;i>RET&lt;/i>/&lt;i>N</pubmed_abstract><journal>Cancers</journal><pagination>3071</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12468581</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Factors Associated with the Detection of Actionable Genomic Alterations Using Liquid Biopsy in Biliary Tract Cancer.</pubmed_title><pmcid>PMC12468581</pmcid><pubmed_authors>Ohira R</pubmed_authors><pubmed_authors>Suzuki R</pubmed_authors><pubmed_authors>Ohira H</pubmed_authors><pubmed_authors>Asama H</pubmed_authors><pubmed_authors>Shimizu H</pubmed_authors><pubmed_authors>Osawa K</pubmed_authors><pubmed_authors>Sato K</pubmed_authors><pubmed_authors>Kudo K</pubmed_authors><pubmed_authors>Sugimoto M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Factors Associated with the Detection of Actionable Genomic Alterations Using Liquid Biopsy in Biliary Tract Cancer.</name><description>&lt;b>Background&lt;/b>: Blood-based comprehensive genomic profiling (CGP), a form of liquid biopsy, is often used for biliary tract cancer (BTC) when tissue-based CGP (tissue CGP) is unavailable, despite lower detection rates. This study explored factors linked to detecting actionable genomic alterations to optimize its use. &lt;b>Methods&lt;/b>: We retrospectively analyzed BTC cases in Japan's C-CAT (June 2019-January 2025), restricting panel comparisons to FoundationOne&lt;sup>®&lt;/sup> CDx (F1; n = 5019) and FoundationOne&lt;sup>®&lt;/sup> Liquid CDx (F1L; n = 1550). Missing covariates were handled by multiple imputations (m = 20). Between-panel balance used 1:1 propensity-score matching (caliper 0.2). Outcomes were modeled with logistic regression. Targets included MSI-H, TMB-H, &lt;i>FGFR2&lt;/i>/&lt;i>RET&lt;/i>/&lt;i>N</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:10:25.072Z</modification><creation>2026-05-02T03:07:38.207Z</creation></dates><accession>S-EPMC12468581</accession><cross_references><pubmed>41008912</pubmed><doi>10.3390/cancers17183071</doi></cross_references></HashMap>