Evidence map›Paper›PMID 29523990›Full record

ArticleInternational journal of colorectal disease2018

Colorectal cancer surveillance in Portuguese families with lynch syndrome: a cohort study.

Rita Vale Rodrigues, Isabel Claro, Pedro Lage, Isadora Rosa, Sara Ferreira, João Pereira da Silva, António Dias Pereira

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Article in International journal of colorectal disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Rita Vale RodriguesGastroenterology Department, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Rua Prof. Lima Basto, 1099-023, Lisbon, Portugal. rita.vale.rodrigues@gmail.com.ORCID http://orcid.org/0000-0001-6191-9852
Isabel ClaroGastroenterology Department and Familial Cancer Risk Clinic, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Lisbon, Portugal.
Pedro LageGastroenterology Department and Familial Cancer Risk Clinic, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Lisbon, Portugal.
Isadora RosaGastroenterology Department and Familial Cancer Risk Clinic, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Lisbon, Portugal.
Sara FerreiraGastroenterology Department and Familial Cancer Risk Clinic, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Lisbon, Portugal.
João Pereira da SilvaGastroenterology Department, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Rua Prof. Lima Basto, 1099-023, Lisbon, Portugal.
António Dias PereiraGastroenterology Department, Instituto Português de Oncologia de Lisboa de Francisco Gentil, Rua Prof. Lima Basto, 1099-023, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLynch syndrome (LS) is associated with a high risk of colorectal cancer (CRC). The aim of this study was to assess the cumulative risk for the development of colorectal adenomas or carcinomas in a LS CRC surveillance program and to audit the quality of the endoscopic procedures.

methodsWe evaluated 147 asymptomatic LS mutation carriers, without previous CRC, in a surveillance program with colonoscopy every 12-18 months, between 2005 and 2016. Data was obtained by retrospective review of colonoscopy reports and hospital clinical files. The main outcome was assessed using Kaplan-Meier curves. Logistic regression was used to study the risk of developing adenomas.

resultsPatients were under surveillance for 1092 observation years (mean, 7.7 years/patient). Most exams presented adequate bowel preparation (83.5%) and 99.2% achieved cecal intubation. The estimated risk for adenomas at age 60 was 75.6% in men (95%CI, 60.5-88.3) and 65.5% in women (95%CI, 50.8-79.7). Male gender (OR 2.4; 95%CI, 1.2-4.9; p = 0.018) and age at start of surveillance > 40 years (OR 3.7; 95%CI, 1.8-7.7; p < 0.001) were independent risk factors for adenoma detection. CRC was diagnosed in 11 patients with an estimated cumulative risk at age 60 of 18.4% (95%CI, 9.2-34.8%); 72.7% of CRC were classified as stage I; no patient died from CRC.

conclusionA colonoscopic surveillance program in LS patients allowed the detection of adenomas in a large group of mutation carriers and diagnosis of early-stage carcinomas. Our findings may help other teams to adopt similar strategies or to refer patients early to specialized centers.

Indexed as

Population SurveillanceAdenomaAdultAgedCohort StudiesColonoscopyColorectal NeoplasmsColorectal Neoplasms, Hereditary NonpolyposisEarly Detection of CancerFamilyFemaleHeterozygoteHumansMaleMiddle AgedMutationAdenomasColonoscopyColorectal cancerLynch syndromeSurveillance

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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.