Evidence map›Paper›PMID 41357375›Full record

ArticleWorld journal of transplantation2025

Association of vascular invasion and tumor differentiation on post-liver transplant outcomes in patients with hepatocellular carcinoma.

Nazlı Begüm Öztürk, Merve M Gurakar, Ximena Parraga, Marwan Alsaqa, Leandro Sierra, Emily Currier, Butros Fakhoury, Alan Bonder, Ahmet Gurakar, Behnam Saberi

Abstract read
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Article in World journal of transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Nazlı Begüm ÖztürkDepartment of Gastroenterology and Hepatology, St. Louis University, St. Louis, MO 63104, United States.
Merve M GurakarDepartment of Gastroenterology and Hepatology, Johns Hopkins School of Medicine, Baltimore, MD 21205, United States.
Ximena ParragaDepartment of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, United States.
Marwan AlsaqaDepartment of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, United States.
Leandro SierraDepartment of Internal Medicine, Cleveland Clinic Foundation, Cleveland, OH 44195, United States.
Emily CurrierDepartment of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, United States.
Butros FakhouryDepartment of Internal Medicine, Virginia Commonwealth University, Richmond, VA 23220, United States.
Alan BonderDepartment of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, United States.
Ahmet GurakarDepartment of Gastroenterology and Hepatology, Johns Hopkins University School of Medicine, Baltimore, MD 21205, United States. aguraka1@jhmi.edu.
Behnam SaberiDepartment of Gastroenterology and Hepatology, Beth Israel Deaconess Medical Center, Boston, MA 02215, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver transplant (LT) is one of the main treatment options in selected patients with hepatocellular carcinoma (HCC). Overall, macrovascular invasion has been shown to be associated with an increased risk of tumor recurrence and mortality after LT in HCC. Macrovascular invasion detected on imaging is often considered a contraindication for LT in HCC.

aimTo investigate the effect of macrovascular invasion in explant on post-LT survival in HCC patients using a large national transplant database in the United States.

methodsLT recipients with HCC between the years 2012 and 2022 were identified by using the United Network for Organ Sharing/Organ Procurement Transplant Network database. Patients who underwent deceased-donor LT with available liver explant pathology data were included. Kaplan-Meier curves were used for survival analysis, and multistep regression analysis was used to determine the predictors of mortality.

resultsA total of 13638 LT recipients with HCC and available explant pathology were included. Of these, 254 (1.8%) showed macrovascular invasion, 1712 (12.6%) had microvascular invasion, and 11672 (85.6%) had absent invasion. Poor tumor differentiation was more common with macrovascular invasion than with microvascular or absent invasion (22.4%, 17.7%, and 5.1%, respectively,

conclusionMacrovascular invasion accounted for a minority of cases at 1.8%. Macrovascular invasion and poor tumor differentiation on liver explants in patients with HCC were associated with significantly higher post-LT mortality, meaning that the extent of tumor involvement and tumor biology are important predictors of post-LT survival in HCC. However, the overall 5-year survival in patients with macrovascular invasion may still be within an acceptable range.

Indexed as

CirrhosisHepatocellular carcinomaRecurrenceTransplantVascular invasion

Identifiers

PMID41357375
PMCPMC12679214

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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.