Evidence map›Paper›PMID 35916920›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2022

Addition of Y-90 radioembolization increases tumor response and local disease control in hepatocellular carcinoma patients receiving sorafenib.

Osman Öcal, Kerstin Schütte, Christoph J Zech, Christian Loewe, Otto van Delden, Vincent Vandecaveye, Chris Verslype, Bernhard Gebauer, Christian Sengel, Irene Bargellini and 13 more

Abstract readMulticenter Study
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
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

23 authors.

Osman ÖcalDepartment of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.
Kerstin SchütteDepartment of Internal Medicine and Gastroenterology, Niels-Stensen-Kliniken Marienhospital, Osnabrück, Germany.
Christoph J ZechRadiology and Nuclear Medicine, University Hospital Basel, University of Basel, Basel, Switzerland.
Christian LoeweSection of Cardiovascular and Interventional Radiology, Department of Bioimaging and Image-Guided Therapy, Medical University of Vienna, Vienna, Austria.
Otto van DeldenDepartment of Radiology and Nuclear Medicine, Academic University Medical Centers, Amsterdam, The Netherlands.
Vincent VandecaveyeDepartment of Radiology, University Hospitals Leuven, Leuven, Belgium.
Chris VerslypeDepartment of Digestive Oncology, University Hospitals Leuven, Leuven, Belgium.
Bernhard GebauerDepartment of Radiology, Charité - University Medicine Berlin, Berlin, Germany.
Christian SengelRadiology Department, Grenoble University Hospital, La Tronche, France.
Irene BargelliniDepartment of Vascular and Interventional Radiology, University Hospital of Pisa, Pisa, Italy.
Roberto IezziUOC di Radiologia, Dipartimento di Diagnostica per Immagini, Radioterapia Oncologica ed Ematologia, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Alexander PhilippDepartment of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Thomas BergKlinik und Poliklinik für Gastroenterologie, Sektion Hepatologie, Universitätsklinikum Leipzig, Leipzig, Germany.
Heinz J KlümpenDepartment of Medical Oncology, Amsterdam University Medical Centers, Amsterdam, the Netherlands.
Julia BenckertDepartment of Hepatology and Gastroenterology, Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.
Maciej PechDepartments of Radiology and Nuclear Medicine, University of Magdeburg, Magdeburg, Germany.
Antonio GasbarriniFondazione Policlinico Universitario Gemelli IRCCS, Universita' Cattolica del Sacro Cuore, Rome, Italy.
Holger AmthauerCorporate member of Freie Universität Berlin and Humboldt Universität zu Berlin, Department of Nuclear Medicine, Charité - Universitätsmedizin Berlin, Augustenburger Platz 1, 13353, Berlin, Germany.
Peter BartensteinDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.
Bruno SangroLiver Unit, Clínica Universidad de Navarra and CIBEREHD, Pamplona, Spain.
Peter MalfertheinerDepartment of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Jens RickeDepartment of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany.
Max SeidenstickerDepartment of Radiology, University Hospital, LMU Munich, Marchioninistrasse 15, 81377, Munich, Germany. max.seidensticker@med.uni-muenchen.de.ORCID 0000-0002-2481-5410

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo compare the treatment response and progression-free survival (PFS) in advanced hepatocellular carcinoma (HCC) patients who received sorafenib treatment either alone or combined with radioembolization (RE).

methodsFollow-up images of the patients treated within a multicenter phase II trial (SORAMIC) were assessed by mRECIST. A total of 177 patients (73 combination arm [RE + sorafenib] and 104 sorafenib arm) were included in this post-hoc analysis. Response and progression characteristics were compared between treatment arms. Survival analyses were done to compare PFS and post-progression survival between treatment arms. Multivariate Cox regression analysis was used to compare survival with factors known to influence PFS in patients with HCC.

resultsThe combination arm had significantly higher objective response rate (61.6% vs. 29.8%, p < 0.001), complete response rate (13.7% vs. 3.8%, p = 0.022), and a trend for higher disease control rate (79.2% vs. 72.1%, p = 0.075). Progression was encountered in 116 (65.5%) patients and was more common in the sorafenib arm (75% vs. 52.0%, p = 0.001). PFS (median 8.9 vs. 5.4 months, p = 0.022) and hepatic PFS were significantly better in the combination arm (9.0 vs. 5.7 months, p = 0.014). Multivariate analysis confirmed the treatment arm as an independent predictor of PFS.

conclusionIn advanced HCC patients receiving sorafenib, combination with RE has an additive anticancer effect on sorafenib treatment resulting in a higher and longer tumor response. However, the enhanced response did not translate into prolonged survival. Better patient selection and superselective treatment could improve outcomes after combination therapy.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsHumansPhenylurea CompoundsSorafenibYttrium RadioisotopesPhenylurea CompoundsSorafenibYttrium-90Yttrium RadioisotopesHepatocellular carcinomamRECISTObjective responseRadioembolizationSorafenib

Identifiers

PMID35916920
PMCPMC9606085

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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.