Evidence map›Paper›PMID 33822277›Full record

ArticleFamilial cancer2022

Malignancy risk in individuals with familial adenomatous polyposis receiving biologics and immunomodulators.

Muhammad Salman Faisal, Carol A Burke, Jean-Paul Achkar, Benjamin Click, Margaret O'Malley, Lisa LaGuardia, Susan Milicia, Brandie Leach, David Liska, James Church and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Familial cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Muhammad Salman FaisalDepartment of Internal Medicine, Cleveland Clinic Foundation, Lerner Research Institute, 2111 East 96th Street, Cleveland, OH, 44195, USA. faisalm@ccf.org.ORCID 0000-0002-3275-0098
Carol A BurkeDepartment of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic Foundation, Cleveland, USA.
Jean-Paul AchkarDepartment of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic Foundation, Cleveland, USA.
Benjamin ClickDepartment of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic Foundation, Cleveland, USA.
Margaret O'MalleyDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
Lisa LaGuardiaDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
Susan MiliciaDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
Brandie LeachDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
David LiskaDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
James ChurchDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
Matthew KaladyDepartment of Colorectal Surgery, Cleveland Clinic Foundation, Cleveland, USA.
Gautam MankaneyDepartment of Gastroenterology, Hepatology and Nutrition, Cleveland Clinic Foundation, Cleveland, USA.
Cleveland Clinic · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinicians may be hesitant to prescribe biologics or immunomodulators to individuals with familial adenomatous polyposis (FAP) and comorbid inflammatory disease (CID) because of increased cancer risk. Our aim was to compare the risk of malignancy in FAP individuals with inflammatory bowel (IBD) and/or rheumatic disease that received biologics/immunomodulators to those who did not. Individuals with FAP and CID were included in the study. We compared the incidence of cancer between individuals exposed to biologics/immunomodulators compared to unexposed from the date of diagnosis of comorbid disease till last follow up or death. Hazard ratio (HR) for cancer was computed using Cox regression model and compared by exposure status to biologic/immunomodulators. 25 individuals with FAP and a comorbid inflammatory disease were identified including 9 (36%) with IBD and 16 (64%) with rheumatic disease. 14 (56%) were exposed to a biologic and or immunomodulator. Median duration of biologic/immunomodulator exposure was 48 (2-180) months. 3 (21.4%) in the exposed group compared to 1 (9.1%) in the unexposed group developed cancer with a HR for exposure of 1.92 (CI 0.2-18.5, p = 0.57). Median duration of follow up after the diagnosis of inflammatory disease was 10 (5.5-17.0) years in the exposed and 6 (3.0-15.0) years in the unexposed group. In the exposed group, 1 patient developed gastric and 2 developed colon cancer. One unexposed patient developed medullary thyroid cancer. There is a possible trend of more cancers in the group that received biologics/immunomodulators-but given the small number of patients and p-value, there may be no difference at all. This preliminary finding warrants study in a larger cohort.

Indexed as

Adenomatous Polyposis ColiBiological ProductsInflammatory Bowel DiseasesRheumatic DiseasesThyroid NeoplasmsHumansImmunologic FactorsBiological ProductsImmunologic FactorsBiologicsFamilial adenomatous polyposisInflammatory bowel disease

Identifiers

PMID33822277
OpenAlexW3144012948

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.