Evidence map›Paper›PMID 39477763›Full record

ArticlePathology2025

Presence and extent of lymphovascular invasion in surgical stage I squamous cell carcinoma of the cervix: a comprehensive, international, multicentre, retrospective clinicopathological study.

Simona Stolnicu, Douglas Allison, Basile Tessier-Cloutier, Amir Momeni-Boroujeni, Lien Hoang, Antonio Ieni, Ana Felix, Cristina Terinte, Anna Pesci, Claudia Mateoiu and 16 more

Abstract readMulticenter Study
In one paragraph

Article in Pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Simona StolnicuDepartment of Pathology, University of Medicine, Pharmacy, Science and Technology 'George E Palade' of Targu Mures, Targu Mures, Romania. Electronic address: simonastolnicu@icloud.com.
Douglas AllisonDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Basile Tessier-CloutierDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Amir Momeni-BoroujeniDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Lien HoangDepartment of Pathology, Vancouver General Hospital, Vancouver, BC, Canada.
Antonio IeniDepartment of Pathology, Universita degli Studi di Messina, Italy.
Ana FelixDepartment of Pathology, Oncologic Institute, Lisbon, Portugal.
Cristina TerinteRegional Institute of Oncology, Iasi, Romania.
Anna PesciOspedale Sacro Cuore Don Calabria, Negrar, Italy.
Claudia MateoiuDepartment of Pathology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Anjelica HodgsonDepartment of Pathology, Laboratory Medicine Program, University Health Network, Toronto, Canada.
Esther GuerraDepartment of Pathology, Hospital Universitari de Bellvitge-IDIBELL, Barcelona, Spain.
Louise de BrotDepartment of Pathology, A.C. Camargo Cancer Center, Sao Paulo, Brazil.
Ricardo R LastraDepartment of Pathology, University of Chicago, Chicago, IL, USA.
Takako KiyokawaJikei University School of Medicine, Tokyo, Japan.
Rouba Ali-FehmiDepartment of Pathology, University of Michigan, Detroit, MI, USA.
Mira KheilDepartment of Pathology, Wayne University, Detroit, MI, USA.
Pavel DundrDepartment of Pathology, First Faculty of Medicine, Charles University and General University Hospital in Prague, Czech Republic.
Andres RomaDepartment of Pathology, University of California, San Diego, USA.
Oluwole FadareDepartment of Pathology, University of California, San Diego, USA.
Gulisa TurashviliDepartment of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, USA.
Esther OlivaDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Kyle M DevinsDepartment of Pathology, Massachusetts General Hospital, Boston, MA, USA.
Glauco BaiocchiDepartment of Surgical Oncology, A.C.Camargo Cancer Center, Brazil.
David CibulaDepartment of Gynaecology, Obstetrics and Neonatology, General University Hospital in Prague, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Robert A SoslowDepartment of Pathology, Cleveland Clinic, Cleveland, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

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 <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 statistical analyses were performed on 97 patients with the International Federation of Gynecology and Obstetrics (FIGO) 2018 stage IA and 329 patients with stage IB SCC of the cervix. LVI, both focal and extensive, was more frequent in stage IB than in stage IA (p<0.001). Patients with stage IB carcinomas with extensive LVI had worse PFS [hazard ratio (HR) 2.86; 95% confidence interval (CI) 1.49, 5.49; p=0.005] and OS (HR 2.88; 95% CI 1.38, 6.02; p=0.012) than those with focal or no LVI. In stage IA, in contrast, the presence and extent of LVI did not associate with PFS (p=0.926) or OS. Extensive LVI was not statistically correlated with PFS and OS in substages IA1, IA2 or IB2. PFS (HR 3.7; 95% CI 1.61, 8.46; p<0.001) and OS (HR 4.18; 95% CI 1.58, 11.04; p=0.002) in stage IB1, and PFS (HR 7.78; 95% CI 0.87, 69.82; p=0.039) in stage IB3 were diminished in the presence of extensive LVI. In conclusion, in patients with FIGO stage I cervical SCC, the presence and extent of LVI has prognostic significance in stage IB carcinoma, and quantifying LVI is recommended.

Indexed as

Carcinoma, Squamous CellNeoplasm StagingUterine Cervical NeoplasmsAdultAgedAged, 80 and overCervix UteriFemaleHumansLymphatic MetastasisMiddle AgedNeoplasm InvasivenessPrognosisRetrospective Studieslymph node metastasislymphovascular invasionprognosissquamous cell carcinomastage

Identifiers

PMID39477763
PMCPMC12447657

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.