Evidence map›Paper›PMID 35501168›Full record

ArticlePathology2022

Clinical correlation of lymphovascular invasion and Silva pattern of invasion in early-stage endocervical adenocarcinoma: proposed binary Silva classification system.

Simona Stolnicu, Lien Hoang, Noorah Almadani, Louise De Brot, Glauco Baiocchi, Graziele Bovolim, Maria Jose Brito, Georgia Karpathiou, Antonio Ieni, Esther Guerra and 11 more

Open access · greenAbstract read
In one paragraph

Article in Pathology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.9field-weighted citation impact, top 6% of its field
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

7 citing papers in PubMed, 22 citations in OpenAlex.

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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

21 authors at 15 institutions in 10 countries.

Simona StolnicuDepartment of Pathology, University of Medicine, Pharmacy, Sciences and Technology, Targu Mures, Romania. Electronic address: stolnicu@gmx.net.
Lien HoangDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, Canada.
Noorah AlmadaniDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, BC, Canada.
Louise De BrotDepartment of Pathology, A.C.Camargo Cancer Center, São Paulo, Brazil.
Glauco BaiocchiDepartment of Surgical Oncology, A.C.Camargo Cancer Center, São Paulo, Brazil.
Graziele BovolimDepartment of Pathology, A.C.Camargo Cancer Center, São Paulo, Brazil.
Maria Jose BritoDepartment of Pathology, Hospital Garcia de Orta, Almada, Portugal.
Georgia KarpathiouDepartment of Pathology, University Hospital of Saint-Etienne, Saint-Priest-en-Jarez, France.
Antonio IeniDepartment of Human Pathology, University of Messina, Messina, Italy.
Esther GuerraDepartment of Pathology, Hospital Universitari de Bellvitge-IDIBELL, Barcelona, Spain.
Takako KiyokawaDepartment of Pathology, Jikei University School of Medicine, Tokyo, Japan.
Pavel DundrDepartment of Pathology, First Medical Faculty, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Carlos Parra-HerranBrigham and Women's Hospital, Boston, MA, USA.
Sofia LériasNOVA Medical School - UNL, Department of Pathology, Instituto Portugues de Oncologia, Lisbon, Portugal.
Ana FelixNOVA Medical School - UNL, Department of Pathology, Instituto Portugues de Oncologia, Lisbon, Portugal.
Andres RomaUniversity of California San Diego, La Jolla, CA, USA.
Anna PesciIRCSS Ospedale Sacro Cuore Don Calabria, Negrar, Italy.
Esther OlivaMassachusetts General Hospital, Boston, MA, USA.
Kay J ParkDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Robert A SoslowDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nadeem R Abu-RustumGynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Department of Obstetrics and Gynaecology, Weill Cornell Medical College, New York, NY, USA.
AC Camargo Hospital · BRMemorial Sloan Kettering Cancer Center · USIPO Porto · PTUniversity of British Columbia · CABellvitge University Hospital · ESBrigham and Women's Hospital · USCharles University · CZHospital Garcia de Orta · PTInstitute Cancer De La Loire Lucien Neuwirth · FRJikei University School of Medicine · JPMassachusetts General Hospital · USOspedale Sacro Cuore Don Calabria · ITUniversitatea de Medicină, Farmacie, Științe și Tehnologie „George Emil Palade” din Târgu Mureș · ROUniversity of California San Diego · USUniversity of Messina · IT

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

Silva invasion pattern can help predict lymph node metastasis risk in endocervical adenocarcinoma. We analysed Silva pattern of invasion and lymphovascular invasion to determine associations with clinical outcomes in stage IA and IB1 endocervical adenocarcinomas. International Federation of Gynecology and Obstetrics (FIGO; 2019 classification) stage IA-IB1 endocervical adenocarcinomas from 15 international institutions were examined for Silva pattern, presence of lymphovascular invasion, and other prognostic parameters. Lymph node metastasis status, local/distant recurrences, and survival data were compared using appropriate statistical tests. Of 399 tumours, 152 (38.1%) were stage IA [IA1, 77 (19.3%); IA2, 75 (18.8%)] and 247 (61.9%) were stage IB1. On multivariate analysis, lymphovascular invasion (p=0.008) and Silva pattern (p<0.001) were significant factors when comparing stage IA versus IB1 endocervical adenocarcinomas. Overall survival was significantly associated with lymph node metastasis (p=0.028); recurrence-free survival was significantly associated with lymphovascular invasion (p=0.002) and stage (1B1 versus 1A) (p=0.002). Five and 10 year overall survival and recurrence-free survival rates were similar among Silva pattern A cases and Silva pattern B cases without lymphovascular invasion (p=0.165 and p=0.171, respectively). Silva pattern and lymphovascular invasion are important prognostic factors in stage IA1-IB1 endocervical adenocarcinomas and can supplement 2019 International Federation of Gynecology and Obstetrics staging. Our binary Silva classification system groups patients into low risk (patterns A and B without lymphovascular invasion) and high risk (pattern B with lymphovascular invasion and pattern C) categories.

Indexed as

AdenocarcinomaCarcinomaUterine Cervical NeoplasmsFemaleHumansLymphatic MetastasisNeoplasm StagingPrognosisRetrospective Studiesendocervical adenocarcinomalymphovascular invasionpattern of invasionSilva patternStage

Identifiers

PMID35501168
PMCPMC9378671
OpenAlexW4225159497

What OpenQuestion holds

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Registered trials

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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.