<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Yang K</submitter><pubmed_abstract>Current methods for the early detection and minimal residual disease (MRD) monitoring of urothelial carcinoma (UC) are invasive and/or possess suboptimal sensitivity. We developed an efficient workflow named urine tumor DNA multidimensional bioinformatic predictor (utLIFE). Using UC-specific mutations and large copy number variations, the utLIFE-UC model was developed on a bladder cancer cohort (n = 150) and validated in The Cancer Genome Atlas (TCGA) bladder cancer cohort (n = 674) and an upper tract urothelial carcinoma (UTUC) cohort (n = 22). The utLIFE-UC model could discriminate 92.8% of UCs with 96.0% specificity and was robustly validated in the BLCA_TCGA and UTUC cohorts. Furthermore, compared to cytology, utLIFE-UC improved the sensitivity of bladder cancer detection (p &lt; 0.01). I</pubmed_abstract><journal>Molecular cancer</journal><pagination>25</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9898696</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Letter to the Editor: clinical utility of urine DNA for noninvasive detection and minimal residual disease monitoring in urothelial carcinoma.</pubmed_title><pmcid>PMC9898696</pmcid><pubmed_authors>Yao L</pubmed_authors><pubmed_authors>Ding F</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Yang K</pubmed_authors><pubmed_authors>Zhou T</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Niu Y</pubmed_authors><pubmed_authors>Guo J</pubmed_authors><pubmed_authors>He Z</pubmed_authors><pubmed_authors>Hu H</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Yu W</pubmed_authors><pubmed_authors>Cao S</pubmed_authors><pubmed_authors>Ye D</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Lou F</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Letter to the Editor: clinical utility of urine DNA for noninvasive detection and minimal residual disease monitoring in urothelial carcinoma.</name><description>Current methods for the early detection and minimal residual disease (MRD) monitoring of urothelial carcinoma (UC) are invasive and/or possess suboptimal sensitivity. We developed an efficient workflow named urine tumor DNA multidimensional bioinformatic predictor (utLIFE). Using UC-specific mutations and large copy number variations, the utLIFE-UC model was developed on a bladder cancer cohort (n = 150) and validated in The Cancer Genome Atlas (TCGA) bladder cancer cohort (n = 674) and an upper tract urothelial carcinoma (UTUC) cohort (n = 22). The utLIFE-UC model could discriminate 92.8% of UCs with 96.0% specificity and was robustly validated in the BLCA_TCGA and UTUC cohorts. Furthermore, compared to cytology, utLIFE-UC improved the sensitivity of bladder cancer detection (p &lt; 0.01). I</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-05-29T19:43:56.67Z</modification><creation>2025-05-29T19:43:56.67Z</creation></dates><accession>S-EPMC9898696</accession><cross_references><pubmed>36739413</pubmed><doi>10.1186/s12943-023-01729-7</doi></cross_references></HashMap>