Evidence map›Paper›PMID 41685088›Full record

ArticleTransplant international : official journal of the European Society for Organ Transplantation2025

Incidental Combined Hepatocellular-Cholangiocarcinoma in Liver Transplant Recipients: A Matched Cohort Study.

Sudha Kodali, Ashton A Connor, David W Victor, Maen Abdelrahim, Ahmed Elaileh, Khush Patel, Elizabeth W Brombosz, Edward A Graviss, Duc T Nguyen, Susan Xu and 15 more

Abstract read
In one paragraph

Article in Transplant international : official journal of the European Society for Organ Transplantation, 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

25 authors.

Sudha KodaliSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Ashton A ConnorSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
David W VictorSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Maen AbdelrahimJC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, United States.
Ahmed ElailehDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Khush PatelDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Elizabeth W BromboszDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Edward A GravissDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Duc T NguyenDepartment of Pediatrics, Baylor College of Medicine, Houston, TX, United States.
Susan XuDepartment of Medicine, Weill Cornell Medical College, New York, NY, United States.
Linda W MooreDepartment of Surgery, Houston Methodist Hospital, Houston, TX, United States.
Mary R SchwartzDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, United States.
Sadhna DhingraDepartment of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, TX, United States.
Tamneet BasraSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Michelle R Jones-PauleySherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Mazen NoureddinSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Constance M MobleySherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Mark J HobeikaSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Caroline J SimonSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Yee Lee CheahSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
Kirk HeyneJC Walter Jr Transplant Center, Houston Methodist Hospital, Houston, TX, United States.
Ahmed O KasebDepartment of Gastrointestinal Medical Oncology, Division of Cancer Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Ashish SahariaSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
A Osama GaberSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.
R Mark GhobrialSherrie and Alan Conover Center for Liver Disease and Transplantation, Houston Methodist Hospital, Houston, TX, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mixed hepatocellular carcinoma (HCC) with cholangiocarcinoma (HCC-CCA) is an aggressive primary liver cancer and difficult to distinguish from HCC using non-invasive methods. Outcomes of patients incidentally diagnosed with HCC-CCA after LT relative to pure HCC with similar tumor burden were investigated. Medical records of patients undergoing LT (n = 1,898) for HCC (n = 493) from 6/2008-9/2023 were reviewed. Patients incidentally diagnosed with HCC-CCA were propensity matched to HCC patients undergoing LT. Independent analyses were performed using pre-LT (Match1; identifiable pre-LT) and explant pathology (Match2, more prognostic) characteristics. Incidental HCC-CCA occurred in 19 (3.9%) patients; all assumed to have HCC pre-LT and received HCC-directed neoadjuvant treatment. When matched on pre-LT characteristics (Match1, n = 57), more patients with HCC-CCA were outside Milan or University of California, San Francisco criteria on explant (p = 0.01). More patients with HCC-CCA underwent neoadjuvant microwave ablation (p = 0.02) compared to HCC Match2 (n = 45) but were otherwise similar demographically and clinically. Overall and recurrence-free survival were lower for HCC-CCA in Match1 (p = 0.003 and p < 0.001, respectively) and Match2 (p < 0.001 and p = 0.001, respectively). HCC-CCA has an aggressive phenotype with high recurrence after LT. Better screening tools and biomarkers are needed to distinguish HCC-CCA from HCC to ensure patients receive appropriate treatment and maximize post-LT outcomes.

Indexed as

Bile Duct NeoplasmsCarcinoma, HepatocellularCholangiocarcinomaLiver NeoplasmsLiver TransplantationAgedCohort StudiesFemaleHumansIncidental FindingsMaleMiddle AgedRetrospective Studiescholangiocarcinomahepatocellular carcinomaliver neoplasmsliver transplantationtransplant oncology

Identifiers

PMID41685088
PMCPMC12890706

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.