Evidence map›Paper›PMID 35863354›Full record

Trial reportEndoscopy2023

Risk of residual neoplasia after a noncurative colorectal endoscopic submucosal dissection for malignant lesions: a multinational study.

João Santos-Antunes, Mathieu Pioche, Felipe Ramos-Zabala, Paolo Cecinato, Francisco J Gallego Rojo, Pedro Barreiro, Catarina Félix, Sandro Sferrazza, Frieder Berr, Andrej Wagner and 14 more

Open access · greenAbstract readMulticenter StudyClinical Trial
PubMed Publisher
In one paragraph

Trial report in Endoscopy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 17 institutions in 7 countries.

João Santos-AntunesGastroenterology Department, Faculty of Medicine, Centro Hospitalar Universitário S. João, Porto, Portugal.ORCID 0000-0003-0614-0576
Mathieu PiocheDepartment of Hepatology and Gastroenterology, Edouard Herriot Hospital, Lyon, France.
Felipe Ramos-ZabalaDepartment of Gastroenterology, Department of Clinical Medical Sciences, Hospital Universitario HM Montepríncipe, HM Hospitales, Universidad San Pablo-CEU, CEU Universities Madrid, Madrid, Spain.ORCID 0000-0003-0365-1231
Paolo CecinatoGastroenterology and Digestive Endoscopy Unit, Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.ORCID 0000-0002-1870-5952
Francisco J Gallego RojoGastroenterology Department, Hospital de Poniente, Almería, Spain.
Pedro BarreiroGastroenterology Department, Centro Hospitalar Lisboa Ocidental EPE, Lisbon, Portugal.
Catarina FélixGastroenterology Department, Centro Hospitalar Lisboa Ocidental EPE, Lisbon, Portugal.ORCID 0000-0002-1605-0200
Sandro SferrazzaGastroenterology and Endoscopy Unit, Santa Chiara Hospital, Trento, Italy.
Frieder BerrDepartment of Internal Medicine I, University Clinics Salzburg, Paracelsus Medical University, Salzburg, Austria.
Andrej WagnerDepartment of Internal Medicine I, University Clinics Salzburg, Paracelsus Medical University, Salzburg, Austria.
Arnaud LemmersDepartment of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Erasme Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.ORCID 0000-0001-6256-0167
Mariana Figueiredo FerreiraDepartment of Gastroenterology, Hepatopancreatology and Digestive Oncology, CUB Erasme Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Eduardo AlbénizNavarrabiomed Research Institute, Complejo Hospitalario de Navarra, Public University of Navarra, IdiSNA, Pamplona, Spain.ORCID 0000-0002-9311-3746
Hugo UchimaDigestive Endoscopy Service, Centro Médico Teknon, Barcelona, Spain.
Ricardo Küttner-MagalhãesGastroenterology Department, Hospital Santo António, Centro Hospitalar Universitário do Porto, Porto, Portugal.ORCID 0000-0002-8522-5756
Carlos FernandesGastroenterology Department, Centro Hospitalar de Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal.
Rui MoraisGastroenterology Department, Faculty of Medicine, Centro Hospitalar Universitário S. João, Porto, Portugal.ORCID 0000-0003-1293-3353
Sunil GuptaDepartment of Gastroenterology and Hepatology, Westmead Hospital, Sydney, Australia.ORCID 0000-0003-3471-8304
Daniel Martinho-DiasDepartment of Community Medicine, Information and Decision in Health, Faculty of Medicine, University of Porto, Porto, Portugal.
Elisabete RiosPathology Department, Faculty of Medicine, Centro Hospitalar Universitário S. João, Porto, Portugal.
Isabel Faria-RamosIpatimup/i3S (Instituto de Investigação e Inovação em Saúde da Universidade do Porto), Porto, Portugal.
Margarida MarquesGastroenterology Department, Faculty of Medicine, Centro Hospitalar Universitário S. João, Porto, Portugal.
Michael J BourkeDepartment of Gastroenterology and Hepatology, Westmead Hospital, Sydney, Australia.
Guilherme MacedoGastroenterology Department, Faculty of Medicine, Centro Hospitalar Universitário S. João, Porto, Portugal.
Hospital de São João · PTParacelsus Medical University · ATUniversité Libre de Bruxelles · BEWestmead Hospital · AUAzienda Sanitaria Unità Locale di Reggio Emilia · ITCentro Hospitalar de Lisboa Ocidental · PTCentro Hospitalar de Vila Nova de Gaia · PTComplejo Hospitalario de Navarra · ESHM Hospitales · ESHôpital Edouard Herriot · FRHospital de Poniente · ESHospital de Santo António · PTHospital Quirón Teknon · ESi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTLusíada University of Lisbon · PTOspedale Santa Chiara · ITUniversidade do Porto · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndoscopic submucosal dissection (ESD) in colorectal lesions is technically demanding and a significant rate of noncurative procedures is expected. We aimed to assess the rate of residual lesions after a noncurative ESD for colorectal cancer (CRC) and to establish predictive scores to be applied in the clinical setting.

methodsRetrospective multicenter analysis of consecutive colorectal ESDs. Patients with noncurative ESDs performed for the treatment of CRC lesions submitted to complementary surgery or with at least one follow-up endoscopy were included.

resultsFrom 2255 colorectal ESDs, 381 (17 %) were noncurative, and 135 of these were performed in CRC lesions. A residual lesion was observed in 24 patients (18 %). Surgery was performed in 96 patients and 76 (79 %) had no residual lesion in the colorectal wall or in the lymph nodes. The residual lesion rate for sm1 cancers was 0 %, and for > sm1 cancers was also 0 % if no other risk factors were present. Independent risk factors for lymph node metastasis were poor differentiation and lymphatic permeation (NC-Lymph score). Risk factors for the presence of a residual lesion in the wall were piecemeal resection, poor differentiation, and positive/indeterminate vertical margin (NC-Wall score).

conclusionsLymphatic permeation or poor differentiation warrant surgery owing to their high risk of lymph node metastasis, mainly in > sm1 cancers. In the remaining cases, en bloc and R0 resections resulted in a low risk of residual lesions in the wall. Our scores can be a useful tool for the management of patients who undergo noncurative colorectal ESDs.

Indexed as

Colorectal NeoplasmsEndoscopic Mucosal ResectionEndoscopyHumansLymphatic MetastasisNeoplasm, ResidualRetrospective StudiesTreatment Outcome

Identifiers

PMID35863354
OpenAlexW4286489727

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.