Evidence map›Paper›PMID 33961627›Full record

ArticlePloS one2021

The impact of portal vein tumor thrombosis on survival in patients with hepatocellular carcinoma treated with different therapies: A cohort study.

Aline Mähringer-Kunz, Verena Steinle, Roman Kloeckner, Sebastian Schotten, Felix Hahn, Irene Schmidtmann, Jan Bernd Hinrichs, Christoph Düber, Peter Robert Galle, Hauke Lang and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Aline Mähringer-KunzDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.ORCID 0000-0002-7082-3745
Verena SteinleDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
Roman KloecknerDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.ORCID 0000-0001-5492-4792
Sebastian SchottenDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
Felix HahnDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
Irene SchmidtmannDepartment of Medical Biostatistics, Epidemiology and Informatics, Johannes Gutenberg University Mainz, Mainz, Germany.ORCID 0000-0001-8743-6752
Jan Bernd HinrichsDepartment of Radiology, Medical School Hannover, Hannover, Germany.
Christoph DüberDepartment of Diagnostic and Interventional Radiology, University Medical Center Mainz, Mainz, Germany.
Peter Robert GalleDepartment of Internal Medicine I, University Medical Center Mainz, Mainz, Germany.
Hauke LangDepartment of General, Visceral and Transplant Surgery, University Medical Center Mainz, Mainz, Germany.ORCID 0000-0001-9303-2148
Arndt WeinmannDepartment of Internal Medicine I, University Medical Center Mainz, Mainz, Germany.
Johannes Gutenberg University Mainz · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPortal vein tumor thrombosis (PVTT) is a frequent complication of hepatocellular carcinoma (HCC), which leads to classification as advanced stage disease (regardless of the degree of PVTT) according to the Barcelona Clinic Liver Cancer Classification. For such patients, systemic therapy is the standard of care. However, in clinical reality, many patients with PVTT undergo different treatments, such as resection, transarterial chemoembolization (TACE), selective internal radiation therapy (SIRT), or best supportive care (BSC). Here we examined whether patients benefited from such alternative therapies, according to the extent of PVTT.

methodsThis analysis included therapy-naïve patients with HCC and PVTT treated between January 2005 and December 2016. PVTT was classified according to the Liver Cancer study group of Japan as follows: Vp1 = segmental PV invasion; Vp2 = right anterior or posterior PV; Vp3 = right or left PV; Vp4 = main trunk. Overall survival (OS) was analyzed for each treatment subgroup considering the extent of PVTT. We performed Cox regression analysis with adjustment for possible confounders. To further attenuate selection bias, we applied propensity score weighting using the inverse probability of treatment weights.

resultsA total of 278 treatment-naïve patients with HCC and PVTT were included for analysis. The median observed OS in months for each treatment modality (resection, TACE/SIRT, sorafenib, BSC, respectively) was 32.4, 8.1, N/A, and 1.7 for Vp1; 10.7, 6.9, 5.5, and 1.2 for Vp2; 6.6, 7.5, 2.9, and 0.6 for Vp3; and 8.0, 3.6, 5.3, and 0.7 for Vp4. Thus, the median OS in the resection group in case of segmental PVTT (Vp1) was significantly longer compared to any other treatment group (all p values <0.01).

conclusionsTreatment strategy for HCC with PVTT should not be limited to systemic therapy in general. The extent of PVTT should be considered when deciding on treatment alternatives. In patients with segmental PVTT (Vp1), resection should be evaluated.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsPortal VeinVenous ThrombosisAgedChemoembolization, TherapeuticCohort StudiesFemaleHumansMaleMiddle AgedRetrospective Studies

Identifiers

PMID33961627
PMCPMC8104403
OpenAlexW3157316531

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.