Evidence map›Paper›PMID 40304945›Full record

ArticleAnnals of surgical oncology2025

Combined Portal and Hepatic Vein Embolization Produces Greater Hypertrophy than Portal Vein Embolization Alone with Similar Post-Hepatectomy Outcomes and is not Impacted by Hepatic Artery Infusion Chemotherapy.

Ankur P Choubey, Joanne F Chou, Kevin C Soares, Alice C Wei, Michael I D'Angelica, William R Jarnagin, Mithat Gonen, Vinod P Balachandran, Jeffrey Drebin, Ernesto Santos and 3 more

Abstract readComparative Study
In one paragraph

Article in Annals of surgical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Ankur P ChoubeyDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Joanne F ChouDepartment of Biostatistics and Epidemiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kevin C SoaresDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Alice C WeiDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Michael I D'AngelicaDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
William R JarnaginDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Mithat GonenDepartment of Biostatistics and Epidemiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Vinod P BalachandranDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Jeffrey DrebinDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ernesto SantosDepartment of Interventional Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Juan C CamachoDepartment of Clinical Sciences, Florida State University College of Medicine, Tallahassee, FL, USA.
T Peter Kingham *Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA. kinghamp@mskcc.org.
Fourat Ridouani *Department of Interventional Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundCombined portal and hepatic vein embolization (cPVE-HVE) induces hypertrophy of future liver remnant before hepatectomy. We compared liver hypertrophy and post-hepatectomy outcomes between cPVE-HVE and portal vein embolization (PVE) alone. PATIENTS AND

methodsConsecutive patient outcomes after cPVE-HVE and PVE were compared across all pathologies for degree of hypertrophy (DH), kinetic growth rate (KGR), impact of hepatic artery infusion chemotherapy (HAIC), and post-hepatectomy complications at a single center.

resultsThe study cohort included 305 patients, 250 underwent PVE and 55 underwent cPVE-HVE. Pre-embolization future liver remnant (FLR) was 28% versus 32% (p < 0.001) for cPVE-HVE and PVE. Post-embolization DH (11.3% versus 9.4%; p = 0.001) and KGR (3.33% versus 2.29%; p < 0.001) were significantly greater for cPVE-HVE over shorter interval (22 versus 28 days; p = 0.007). HAIC was used in 42% (n = 23) of patients before cPVE-HVE and did not impact hypertrophy. Post-hepatectomy outcomes were similar between cPVE-HVE (n = 38) and PVE (n = 250) cohorts. Rates of transfusion (39% versus 40%; p > 0.9), liver failure (7.9% versus 9.2%, p = 0.6), grade 3-5 complications (42% versus 42%, p > 0.9), 90 day all-cause mortality (5.3% versus 3.6%, p = 0.6), and median hospitalization (7 versus 8 days; p = 0.067) were not significantly different.

conclusionscPVE-HVE was associated with greater hypertrophy than PVE alone, with similar post-hepatectomy outcomes. cPVE-HVE after HAIC was safe with similar hypertrophy. Randomized clinical trial evidence is needed to clearly delineate indication for cPVE-HVE and assess postoperative outcomes.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularEmbolization, TherapeuticHepatectomyHepatic VeinsLiver NeoplasmsPortal VeinPostoperative ComplicationsAgedCombined Modality TherapyFemaleFollow-Up StudiesHepatic ArteryHumansHypertrophyInfusions, Intra-ArterialCombined portal vein embolization and hepatic vein embolizationDegree of hypertrophyHepatic artery infusion chemotherapyHepatic artery infusion pumpKinetic growth ratePortal vein embolizationPost-hepatectomy liver failure

Identifiers

PMID40304945
PMCPMC13262762

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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.