Evidence map›Paper›PMID 34609076›Full record

ArticleUnited European gastroenterology journal2021

Lymphovascular invasion quantification could improve risk prediction of lymph node metastases in patients with submucosal (T1b) esophageal adenocarcinoma.

Steffi E M van de Ven, Lucia Suzuki, Annieke W Gotink, Fiebo J C Ten Kate, Daan Nieboer, Bas L A M Weusten, Lodewijk A A Brosens, Richard van Hillegersberg, Lorenza Alvarez Herrero, Cees A Seldenrijk and 21 more

Abstract read
In one paragraph

Article in United European gastroenterology journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

31 authors.

Steffi E M van de VenDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-9793-0957
Lucia SuzukiDepartment of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Annieke W GotinkDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.ORCID 0000-0003-0509-3472
Fiebo J C Ten KateDepartment of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Daan NieboerDepartment of Public Health, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Bas L A M WeustenDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.
Lodewijk A A BrosensDepartment of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.
Richard van HillegersbergDepartment of Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
Lorenza Alvarez HerreroDepartment of Gastroenterology and Hepatology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Cees A SeldenrijkDepartment of Pathology, Pathology DNA, St. Antonius Hospital, Nieuwegein, The Netherlands.
Alaa AlkhalafDepartment of Gastroenterology and Hepatology, Isala Clinics, Zwolle, The Netherlands.
Freek C P MollDepartment of Pathology, Isala Clinics, Zwolle, The Netherlands.
Wouter CurversDepartment of Gastroenterology and Hepatology, Catharina Hospital, Eindhoven, The Netherlands.
Ineke G van LijnschotenDepartment of Pathology, PAMM, Eindhoven, The Netherlands.
Thjon J TangDepartment of Gastroenterology and Hepatology, Ijsselland Hospital, Capelle aan den Ijssel, The Netherlands.
Hans van der ValkDepartment of Pathology, Ijselland Hospital, Capelle aan den Ijssel, The Netherlands.
Wouter B NagengastDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, The Netherlands.
Gursah Kats-UgurluDepartment of Pathology, University Medical Center Groningen, Groningen, The Netherlands.
John T M PlukkerDepartment of Surgery, University Medical Center Groningen, Groningen, The Netherlands.
Martin H M G HoubenDepartment of Gastroenterology and Hepatology, Haga Teaching Hospital, Den Haag, The Netherlands.
Jaap S van der LaanDepartment of Pathology, Haga Teaching Hospital, Den Haag, The Netherlands.
Roos E PouwDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.ORCID 0000-0002-4707-1186
Jacques J G H M BergmanDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Sybren L MeijerDepartment of Pathology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Mark I van Berge HenegouwenDepartment of Surgery, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Bas P L WijnhovenDepartment of Surgery, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Pieter J F de JongeDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Michael DoukasDepartment of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Marco J BrunoDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Katharina BiermannDepartment of Pathology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.
Arjun D KochDepartment of Gastroenterology and Hepatology, Erasmus MC Cancer Institute, University Medical Center, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo quantify lymphovascular invasion (LVI) and to assess the prognostic value in patients with pT1b esophageal adenocarcinoma.

methodsIn this nationwide, retrospective cohort study, patients were included if they were treated with surgery or endoscopic resection for pT1b esophageal adenocarcinoma. Primary endpoint was the presence of metastases, lymph node metastases, or distant metastases, in surgical resection specimens or during follow-up. A prediction model to identify risk factors for metastases was developed and internally validated.

results248 patients were included. LVI was distributed as follows: no LVI (n = 196; 79.0%), 1 LVI focus (n = 16; 6.5%), 2-3 LVI foci (n = 21; 8.5%) and ≥4 LVI foci (n = 15; 6.0%). Seventy-eight patients had metastases. The risk of metastases was increased for tumors with 2-3 LVI foci [subdistribution hazard ratio (SHR) 3.39, 95% confidence interval (CI) 2.10-5.47] and ≥4 LVI foci (SHR 3.81, 95% CI 2.37-6.10). The prediction model demonstrated a good discriminative ability (c-statistic 0.81).

conclusionThe risk of metastases is higher when more LVI foci are present. Quantification of LVI could be useful for a more precise risk estimation of metastases. This model needs to be externally validated before implementation into clinical practice.

Indexed as

Lymphatic MetastasisAdenocarcinomaAgedEsophageal NeoplasmsFemaleHumansLymph NodesMaleMiddle AgedNeoplasm InvasivenessRegression AnalysisRetrospective StudiesRisk Factorsendoscopic mucosal resectionesophagectomy lLymphovascular invasionLVIlymph node metastasespredictionquantificationrisk assessmentsubmucosal esophageal adenocarcinomaT1b adenocarcinoma

Identifiers

PMID34609076
PMCPMC8598963

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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.