<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stolnicu S</submitter><funding>National Cancer Institute Division of Cancer Epidemiology and Genetics</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>17-26</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12447657</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>57(1)</volume><pubmed_abstract>The aim of this study was to determine whether the presence and extent of lymphovascular invasion (LVI) is prognostic in surgical stage I cervical squamous cell carcinoma (SCC). All available tumour slides and/or paraffin blocks from 426 patients with stage I cervical SCC treated surgically with curative intent were collected from 18 institutions and retrospectively analysed. Presence and extent of LVI (focal &lt;5 spaces, extensive ≥5 spaces) were assessed on scanning magnification in large haematoxylin and eosin slide sets in 366 cases. Progression-free survival (PFS) was calculated as the time from surgery to first progression or death or last follow-up, whichever occurred first. Overall survival (OS) was defined as the time from surgery to death or last follow-up. Clinicopathological and </pubmed_abstract><journal>Pathology</journal><pubmed_title>Presence and extent of lymphovascular invasion in surgical stage I squamous cell carcinoma of the cervix: a comprehensive, international, multicentre, retrospective clinicopathological study.</pubmed_title><pmcid>PMC12447657</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><pubmed_authors>Ali-Fehmi R</pubmed_authors><pubmed_authors>Fadare O</pubmed_authors><pubmed_authors>Cibula D</pubmed_authors><pubmed_authors>Hoang L</pubmed_authors><pubmed_authors>Pesci A</pubmed_authors><pubmed_authors>Oliva E</pubmed_authors><pubmed_authors>Turashvili G</pubmed_authors><pubmed_authors>Ieni A</pubmed_authors><pubmed_authors>Felix A</pubmed_authors><pubmed_authors>Guerra E</pubmed_authors><pubmed_authors>Dundr P</pubmed_authors><pubmed_authors>Kiyokawa T</pubmed_authors><pubmed_authors>Hodgson A</pubmed_authors><pubmed_authors>Mateoiu C</pubmed_authors><pubmed_authors>Devins KM</pubmed_authors><pubmed_authors>Allison D</pubmed_authors><pubmed_authors>Momeni-Boroujeni A</pubmed_authors><pubmed_authors>Baiocchi G</pubmed_authors><pubmed_authors>Roma A</pubmed_authors><pubmed_authors>Lastra RR</pubmed_authors><pubmed_authors>Soslow RA</pubmed_authors><pubmed_authors>de Brot L</pubmed_authors><pubmed_authors>Kheil M</pubmed_authors><pubmed_authors>Tessier-Cloutier B</pubmed_authors><pubmed_authors>Terinte C</pubmed_authors><pubmed_authors>Stolnicu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Presence and extent of lymphovascular invasion in surgical stage I squamous cell carcinoma of the cervix: a comprehensive, international, multicentre, retrospective clinicopathological study.</name><description>The aim of this study was to determine whether the presence and extent of lymphovascular invasion (LVI) is prognostic in surgical stage I cervical squamous cell carcinoma (SCC). All available tumour slides and/or paraffin blocks from 426 patients with stage I cervical SCC treated surgically with curative intent were collected from 18 institutions and retrospectively analysed. Presence and extent of LVI (focal &lt;5 spaces, extensive ≥5 spaces) were assessed on scanning magnification in large haematoxylin and eosin slide sets in 366 cases. Progression-free survival (PFS) was calculated as the time from surgery to first progression or death or last follow-up, whichever occurred first. Overall survival (OS) was defined as the time from surgery to death or last follow-up. Clinicopathological and </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2026-06-14T06:05:40.559Z</modification><creation>2026-06-14T03:15:14.872Z</creation></dates><accession>S-EPMC12447657</accession><cross_references><pubmed>39477763</pubmed><doi>10.1016/j.pathol.2024.07.008</doi></cross_references></HashMap>