Evidence map›Paper›PMID 32075608›Full record

ArticleBMC cancer2020

Retrospective analysis of the immunogenic effects of intra-arterial locoregional therapies in hepatocellular carcinoma: a rationale for combining selective internal radiation therapy (SIRT) and immunotherapy.

Ligia Craciun, Roland de Wind, Pieter Demetter, Valerio Lucidi, Ali Bohlok, Sébastien Michiels, Fikri Bouazza, Michael Vouche, Ilario Tancredi, Gontran Verset and 9 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07482059 (A Multicenter Phase Ib/II Clinical Study on the Safety and Efficacy of Selective Internal Radiation Therapy), which is not on this map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 5% 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.

NCT07482059 phase1 / phase2recruitingnot on this mapstarted 2026, after this paper: background citation

A Multicenter Phase Ib/II Clinical Study on the Safety and Efficacy of Selective Internal Radiation Therapy (SIRT) With Yttrium-90 Microspheres in Combination With Nivolumab, Ipilimumab, and Lenvatinib in Patients With Unresectable Hepatocellular Carcinoma

TypeinterventionalSponsorWest China HospitalRan2026 to 2028Enrolled33ConditionsUnresectable Hepatocellular CarcinomaArmsttrium-90 microspheres in combination with nivolumab, ipilimumab, and lenvatinib in patients with unresectable hepatocellular carcinoma
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

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  20. New frontiers in radioembolization.Therapeutic advances in medical oncology · 2024
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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

19 authors at 1 institution in 1 country.

Ligia CraciunPathology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Roland de WindPathology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Pieter DemetterPathology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Valerio LucidiAbdominal Surgery, Hôpital Erasme, Université Libre de Bruxelles, Bruxelles, Belgium.
Ali BohlokSurgery, Institut Jules Bordet, Université Libre de Bruxelles, Rue Héger-Bordet, 1, B-1000, Brussels, Belgium.
Sébastien MichielsSurgery, Institut Jules Bordet, Université Libre de Bruxelles, Rue Héger-Bordet, 1, B-1000, Brussels, Belgium.
Fikri BouazzaSurgery, Institut Jules Bordet, Université Libre de Bruxelles, Rue Héger-Bordet, 1, B-1000, Brussels, Belgium.
Michael VoucheRadiology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Ilario TancrediRadiology, Hôpital Erasme, Université Libre de Bruxelles, Bruxelles, Belgium.
Gontran VersetGastroenterology and Medical Oncology, Hôpital Erasme, Université Libre de Bruxelles, Bruxelles, Belgium.
Soizic GaraudMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Céline NaveauxMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Maria Gomez GaldonPathology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Karen Willard GalloMolecular Immunology Unit, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Alain HendliszMedical Oncology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Ivan Duran DerijckereNuclear Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Patrick FlamenNuclear Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Denis LarsimontPathology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.
Vincent DonckierSurgery, Institut Jules Bordet, Université Libre de Bruxelles, Rue Héger-Bordet, 1, B-1000, Brussels, Belgium. vincent.donckier@bordet.be.ORCID http://orcid.org/0000-0003-1457-2520
Université Libre de Bruxelles · BE

Funding

Amis de l'Institut Bordet NA
6 · The paper itself

Abstract

backgroundImmunotherapy represents a promising option for treatment of hepatocellular carcinoma (HCC) in cirrhotic patients but its efficacy is currently inconsistent and unpredictable. Locoregional therapies inducing immunogenic cell death, such as transarterial chemoembolization (TACE) or selective internal radiation therapy (SIRT), have the potential to act synergistically with immunotherapy. For the development of new approaches combining locoregional treatments with immunotherapy, a better understanding of the respective effects of TACE and SIRT on recruitment and activation of immune cells in HCC is needed. To address this question, we compared intra-tumor immune infiltrates in resected HCC after preoperative treatment with TACE or SIRT.

methodsData fromr patients undergoing partial hepatectomy for HCC, without preoperative treatment (SURG, n = 32), after preoperative TACE (TACE, n = 16), or preoperative SIRT (n = 12) were analyzed. Clinicopathological factors, tumor-infiltrating lymphocytes (TILs), CD4

resultsClinicopathological and surgical characteristics were similar in the three groups. A significant increase in TILs, CD4

conclusionsSIRT significantly promotes recruitment/activation of intra-tumor effector-type immune cells compared to TACE or no preoperative treatment. These results suggest that SIRT is a better candidate than TACE to be combined with immunotherapy for treatment of HCC. Evaluation of the optimal doses for SIRT for producing an immunogenic effect and the type of immunotherapy to be used require further evaluation in prospective studies.

Indexed as

AdultAgedAged, 80 and overBrachytherapyCarcinoma, HepatocellularCD8-Positive T-LymphocytesChemoembolization, TherapeuticCombined Modality TherapyFemaleHepatectomyHumansImmunogenic Cell DeathImmunotherapyInfusions, Intra-ArterialLiver NeoplasmsMaleRadiopharmaceuticalsHepatocellular carcinomaImmunotherapyLocoregional therapySelective internal radiation therapy (SIRT)Transarterial chemoembolization (TACE)Tumor-infiltrating lymphocytes

Identifiers

PMID32075608
PMCPMC7032008
OpenAlexW3007223568

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.