Evidence map›Paper›PMID 36757514›Full record

ArticleAnnals of surgical oncology2023

Fistula-Associated Anal Adenocarcinoma: A 20-Year Single-Center Experience.

Felix Harpain, Christopher Dawoud, Kerstin Wimmer, Lukas Schlager, Sabine Kirchnawy, David Rizk, Kerollos Girgis, Eva Mittermair, Felicitas Oberndorfer, Katharina Wöran and 3 more

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Article in Annals of surgical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Nonfistulizing Perianal Crohn's Disease.Clinics in colon and rectal surgery · 2025
    Review
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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

13 authors at 2 institutions in 1 country.

Felix HarpainDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Christopher DawoudDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Kerstin WimmerDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Lukas SchlagerDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Sabine KirchnawyDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
David RizkDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Kerollos GirgisDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Eva MittermairHospital Pharmacy, Klinik Ottakring - Wiener Gesundheitsverbund, Vienna, Austria.
Felicitas OberndorferDepartment of Pathology, Medical University Vienna, Vienna, Austria.
Katharina WöranDepartment of Pathology, Medical University Vienna, Vienna, Austria.
Stefan RissDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Anton StiftDepartment of General Surgery, Division of Visceral Surgery, Medical University of Vienna, Vienna, Austria.
Judith StiftDepartment of Pathology, Medical University Vienna, Vienna, Austria. Judith.stift@gmail.com.
Medical University of Vienna · ATWiener Krankenanstaltenverbund · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFistula-associated anal adenocarcinoma (FAAC) is a rare consequence in patients with long-standing perianal fistulas. A paucity of data are available for this patient collective, making clinical characterization and management of this disease difficult.

objectiveThis study aimed to describe a single-center experience with FAAC patients, their clinical course, and histopathological and molecular pathological characterization.

methodsAll patients receiving surgery for an anal fistula in 1999-2019 at a tertiary university referral hospital were included in this retrospective analysis. Patients with FAAC were eligible for histopathological analysis, including immunohistochemistry and molecular profiling.

resultsThis study included 1004 patients receiving surgical treatment for an anal fistula, of whom 242 had an underlying inflammatory bowel disease (IBD). Ten patients were diagnosed with a fistula-associated anal carcinoma (1.0%), and six of these patients had an FAAC (0.6%). The mean overall survival of FAAC patients was 24 ± 3 months. FAAC immunohistochemistry revealed positive staining for CK20, CDX2 and MUC2, while stainings for CK5/6 and CK7 were negative. All FAAC specimens revealed microsatellite stability. Molecular profiling detected mutations in 35 genes, with the most frequent mutations being TP53, NOTCH1, NOTCH3, ATM, PIK3R1 and SMAD4.

conclusionFAAC is rare but associated with poor clinical outcome. Tissue acquisition is crucial for early diagnosis and therapy and should be performed in long-standing, non-healing, IBD-associated fistulas in particular. The immunophenotype of FAAC seems more similar to the rectal-type mucosa than the anal glands.

Indexed as

AdenocarcinomaAnus NeoplasmsInflammatory Bowel DiseasesRectal FistulaAnal CanalHumansRetrospective StudiesTreatment Outcome

Identifiers

PMID36757514
OpenAlexW4319656176

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.