<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu M</submitter><funding>NCI NIH HHS</funding><pagination>45-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9153261</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(2)</volume><pubmed_abstract>&lt;h4>Introduction&lt;/h4>For maximum utility of molecular characterization by next-generation sequencing (NGS) and better understanding of tumor microenvironment with immune correlates analysis, biopsy specimens must yield adequate tumor tissue, and sequential biopsy specimens should sample a consistent site. We developed a web-based lesion selection tool (LST) that enables management and tracking of the biopsy specimen collections.&lt;h4>Methods&lt;/h4>Of 145 patients, the LST was used for 88 patients; the other 57 served as controls. We evaluated consistency of the lesion biopsied in longitudinal collections, number of cores obtained, and cores with adequate tumor cellularity for NGS. The Fisher exact test and Wilcoxon rank sum test were used to identify differences between the groups.&lt;h4>Results&lt;</pubmed_abstract><journal>Journal of immunotherapy and precision oncology</journal><pubmed_title>Implementation of a Novel Web-Based Lesion Selection Tool to Improve Acquisition of Tumor Biopsy Specimens.</pubmed_title><pmcid>PMC9153261</pmcid><funding_grant_id>P30 CA016672</funding_grant_id><pubmed_authors>Hajjar J</pubmed_authors><pubmed_authors>Fu S</pubmed_authors><pubmed_authors>Pant S</pubmed_authors><pubmed_authors>Nagarajan P</pubmed_authors><pubmed_authors>Carter B</pubmed_authors><pubmed_authors>Roy-Chowdhuri S</pubmed_authors><pubmed_authors>Sabir S</pubmed_authors><pubmed_authors>Tapia C</pubmed_authors><pubmed_authors>Stephen B</pubmed_authors><pubmed_authors>Sun R</pubmed_authors><pubmed_authors>Gong J</pubmed_authors><pubmed_authors>Karp DD</pubmed_authors><pubmed_authors>Javle M</pubmed_authors><pubmed_authors>Koay EJ</pubmed_authors><pubmed_authors>Xu M</pubmed_authors><pubmed_authors>Meric-Bernstam F</pubmed_authors><pubmed_authors>Le H</pubmed_authors><pubmed_authors>Wistuba II</pubmed_authors><pubmed_authors>Aung PP</pubmed_authors><pubmed_authors>Rodon J</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Abdelsalam ME</pubmed_authors><pubmed_authors>Jhingran A</pubmed_authors><pubmed_authors>Colen R</pubmed_authors><pubmed_authors>Naing A</pubmed_authors><pubmed_authors>Hwu P</pubmed_authors><pubmed_authors>Milton DR</pubmed_authors><pubmed_authors>Zarifa A</pubmed_authors><pubmed_authors>Yang V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Implementation of a Novel Web-Based Lesion Selection Tool to Improve Acquisition of Tumor Biopsy Specimens.</name><description>&lt;h4>Introduction&lt;/h4>For maximum utility of molecular characterization by next-generation sequencing (NGS) and better understanding of tumor microenvironment with immune correlates analysis, biopsy specimens must yield adequate tumor tissue, and sequential biopsy specimens should sample a consistent site. We developed a web-based lesion selection tool (LST) that enables management and tracking of the biopsy specimen collections.&lt;h4>Methods&lt;/h4>Of 145 patients, the LST was used for 88 patients; the other 57 served as controls. We evaluated consistency of the lesion biopsied in longitudinal collections, number of cores obtained, and cores with adequate tumor cellularity for NGS. The Fisher exact test and Wilcoxon rank sum test were used to identify differences between the groups.&lt;h4>Results&lt;</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-05-27T20:31:44.06Z</modification><creation>2025-02-19T02:44:23.203Z</creation></dates><accession>S-EPMC9153261</accession><cross_references><pubmed>35663531</pubmed><doi>10.36401/JIPO-21-5</doi><doi>10.36401/jipo-21-5</doi></cross_references></HashMap>