Evidence map›Paper›PMID 35116232›Full record

ArticleWorld journal of clinical oncology2022

Association of cancer with comorbid inflammatory conditions and treatment in patients with Lynch syndrome.

Muhammad S Faisal, Carol A Burke, David Liska, Amy L Lightner, Brandie Leach, Margaret O'Malley, Lisa LaGuardia, Benjamin Click, J P Achkar, Matthew Kalady and 2 more

Open access · diamondAbstract read
In one paragraph

Article in World journal of clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

12 authors at 4 institutions in 2 countries.

Muhammad S FaisalDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
Carol A BurkeDepartment of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH 44195, United States.
David LiskaDepartment of Colorectal Surgery, Cleveland Clinic, Cleveland, OH 44195, United States.
Amy L LightnerDepartment of Colorectal Surgery, Cleveland Clinic, Cleveland, OH 44195, United States.
Brandie LeachCenter for Personalized Genetic Healthcare, Genomic Medicine Institute, Cleveland, OH 44195, United States.
Margaret O'MalleyDepartment of Colorectal Surgery, Cleveland Clinic, Cleveland, OH 44195, United States.
Lisa LaGuardiaDepartment of Colorectal Surgery, Cleveland Clinic, Cleveland, OH 44195, United States.
Benjamin ClickDepartment of Gastroenterology, Hepatology, & Nutrition, Cleveland Clinic, Cleveland, OH 44195, United States.
J P AchkarCenter for Inflammatory Bowel Disease, Department of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic, Cleveland, OH 44195, United States.
Matthew KaladyDepartment of Colorectal Surgery, Ohio State University, Columbus, OH 43210, United States.
J M ChurchDepartment of Colorectal Surgery, Cleveland Clinic, Cleveland, OH 44195, United States.
Gautam MankaneyDepartment of Gastroenterology and Hepatology, Virginia Mason Franciscan Health, Seattle, WA 98101, United States. mankaneg@gmail.com.
Cleveland Clinic · USCenter for Genomic Science · ITFranciscan Health · USThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIndividuals with Lynch syndrome (LS) and hereditary non-polyposis colorectal cancer (HNPCC) are at increased risk of both colorectal cancer and other cancers. The interplay between immunosuppression, a comorbid inflammatory condition (CID), and HNPCC on cancer risk is unclear.

aimTo evaluate the impact of CIDs, and exposure to monoclonal antibodies and immunomodulators, on cancer risk in individuals with HNPCC.

methodsIndividuals prospectively followed in a hereditary cancer registry with LS/HNPCC with the diagnosis of inflammatory bowel disease or rheumatic disease were identified. We compared the proportion of patients with cancer in LS/HNPCC group with and without a CID. We also compared the proportion of patients who developed cancer following a CID diagnosis based upon exposure to immunosuppressive medications.

resultsA total of 21 patients with LS/HNPCC and a CID were compared to 43 patients with LS/HNPCC but no CID. Cancer occurred in 84.2% with a CID compared to 76.7% without a CID (

conclusionIn patients with LS/HNPCC, the presence of a concurrent inflammatory condition, or use of immunosuppressive medication to treat the inflammatory condition, might not increase the rate of cancer occurrence in this limited study.

Indexed as

BiologicsHereditary non-polyposis colorectal cancerImmunosuppressionInflammatory bowel diseaseLynch syndrome

Identifiers

PMID35116232
PMCPMC8790302
OpenAlexW4207067785

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.