Evidence map›Paper›PMID 41216273›Full record

ArticleTranslational gastroenterology and hepatology2025

Sex disparities in liver transplantation for hepatocellular carcinoma: long-term outcomes and recurrence predictors.

Nada El-Domiaty, Audrey Coilly, María Lynch-Mejía, Alina Pascale, Rodolphe Sobesky, Oriana Ciacio, Gabriella Pittau, Wafaa Ibrahim, Chady Salloum, Eleonora De Martin and 8 more

Abstract read
In one paragraph

Article in Translational gastroenterology and hepatology, 2025. 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
–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

1 citing paper in PubMed.

  1. Article
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

18 authors.

Nada El-DomiatyAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.ORCID https://orcid.org/0000-0002-7098-0230
Audrey CoillyAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
María Lynch-MejíaFaculty of Medicine, University of Costa Rica & Gastroenterology Department, San Juan de Dios Hospital, San José, Costa Rica.
Alina PascaleAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Rodolphe SobeskyAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Oriana CiacioAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Gabriella PittauAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Wafaa IbrahimStatistics Department, Faculty of Economics and Political Science, Cairo University, Cairo, Egypt.
Chady SalloumAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Eleonora De MartinAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Antonio Sa CunhaAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Daniel AzoulayAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Eric VibertAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
René AdamAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Didier SamuelAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Olivier RosemorducAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Daniel CherquiAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.
Faouzi SalibaAP-HP Hôpital Paul Brousse, Hepato-Biliary Centre, INSERM UMR 1193 & Université Paris Saclay, Villejuif, France.ORCID https://orcid.org/0000-0002-2058-9217

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: With a 2- to 3-fold higher incidence in men, hepatocellular carcinoma (HCC) is the leading indication for liver transplantation (LT). Despite this sex disparity in HCC incidence, the influence of recipient sex on long-term LT outcomes, including HCC recurrence, is not well established. This study investigates the impact of recipient sex on the long-term outcomes following LT for HCC. Methods: All consecutive patients undergoing LT for HCC between 2005 and 2018 were retrospectively analyzed. Data regarding patient demographics, tumor characteristics, and post-transplant outcomes were collected, and recipients were stratified by sex. Kaplan-Meier analysis was used to assess overall and recurrence-free survival (RFS). Multivariable Cox regression models were then used to determine independent predictors of HCC recurrence within each sex group. Results: Of the 384 adult recipients (mean age was 58.7±8.4 years and mean follow-up of 86.5±51.5 months), 17.2% of patients were female. The main etiology of cirrhosis in the female and male groups was alcohol-related (19.7%, 36.5%), HCV (40.9%, 24.5%) and metabolic dysfunction-associated steatohepatitis (MASH) (10.6%, 12.3%). The Model for End-Stage Liver Disease (MELD) and Child-Pugh scores were similar in both groups. 87.9% and 76.4% of the patients were within the Milan criteria and 95.5% and 91.5% of the patients had an alpha-fetoprotein (AFP) score ≤2 at the time of LT, respectively. The 1-, 3-, 5-, 10- and 15-year survival rates were similar in the male and female groups (91.5%, 81.5%, 72.4%, 57.7% and 44.9% Conclusions: Recipient sex does not impact long-term survival or HCC recurrence after LT. However, sex-specific predictors of HCC recurrence were identified: AFP score >2 and prior hepatectomy in females, and these plus diabetes mellitus and older age in males. Furthermore, female recipients presented with a significantly lower incidence of alcohol-associated cirrhosis as the underlying cause of HCC.

Indexed as

disparityhepatocellular carcinoma (HCC)liver transplantation (LT)recurrenceSex

Identifiers

PMID41216273
PMCPMC12596422

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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.