Evidence map›Paper›PMID 39890667›Full record

ArticleFamilial cancer2025

Thirty-year compliance with a surveillance program for patients with familial adenomatous polyposis.

Boris Cleret de Langavant, Jéremie H Lefèvre, Julie Metras, Antoine Dardenne, Lauren V O'Connell, Maxime Collard, Yann Parc

Abstract read
PubMed Publisher
In one paragraph

Article in Familial cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Boris Cleret de LangavantDepartment of Digestive Surgery, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France.
Jéremie H LefèvreDepartment of Digestive Surgery, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France.
Julie MetrasPred If Centre, Oncogenetic Departement, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France.
Antoine DardennePred If Centre, Oncogenetic Departement, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France.
Lauren V O'ConnellCentre for Colorectal Disease, St. Vincent's University Hospital, Elm Park, Dublin 4, Ireland.
Maxime CollardDepartment of Digestive Surgery, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France.
Yann ParcDepartment of Digestive Surgery, Sorbonne University, Hôpital Saint Antoine, APHP, Paris, 75012, France. yann.parc@aphp.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial adenomatous polyposis is an inherited genetic disorder responsible for multiple anomalies. Lifelong surveillance protocols are essential to detect and prevent adverse developments. However, limited data exist regarding the long-term feasibility of such programs. This study aims to evaluate the compliance with a surveillance program for patients with familial adenomatous polyposis. The study collated data from all patients who underwent surgery between January 1981 and December 1993, excluding non-French residents. Recorded characteristics included medical history, follow-up results, the indications for operations or other procedures, outcomes of these interventions, and patient status at the end of the follow-up period. One hundred and sixty-four patients were enrolled, comprising 86 females (52.4%). The median age at the time of colorectal resection was 29.6 years [10-67]. Thirty-six (22.0%) were diagnosed with cancer at the time of their surgery. Fifty-eight patients (35.3%) passed away at a median age of 52 years [18-95]. During the follow-up period, 47 patients developed duodenal or reservoir adenomas requiring invasive procedures, or desmoid tumors necessitating treatment. After a possible 30 years of follow-up, 49 survivors (46.2%) are still under observation, while 57 (53.8%) have been lost to follow-up. After 30 years of follow-up, the survival rate was 74.2% for patients who remained under observation, but only 58.2% for those lost to follow-up. Long-term follow-up of patients with familial adenomatous polyposis is associated with a high rate of loss to follow-up. However, those who remain under observation maintain an excellent prognosis. Understanding the reasons for loss to follow-up is challenging but may help in reducing this high attrition rate.

Indexed as

Adenomatous Polyposis ColiPatient ComplianceAdolescentAdultAgedAged, 80 and overChildFemaleFollow-Up StudiesHumansMaleMiddle AgedPopulation SurveillanceYoung Adult

Identifiers

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.