Evidence map›Paper›PMID 39333610›Full record

ArticleScientific reports2024

The impact of lenvatinib on sarcopenia in patients with advanced unresectable hepatocellular carcinoma.

Michael Praktiknjo, Ana S Pena Solano, Farsaneh Sadeghlar, Thomas Welchowski, Matthias Schmid, Christian Möhring, Taotao Zhou, Robert Mahn, Malte B Monin, Carsten Meyer and 12 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Michael Praktiknjo *Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Ana S Pena Solano *Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Farsaneh SadeghlarDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Thomas WelchowskiDepartment of Medical Biometry, Informatics and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.
Matthias SchmidDepartment of Medical Biometry, Informatics and Epidemiology (IMBIE), University Hospital Bonn, Bonn, Germany.
Christian MöhringDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Taotao ZhouDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Robert MahnDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Malte B MoninDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Carsten MeyerDepartment of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany.
Georg FeldmannDepartment of Internal Medicine III, University Hospital Bonn, Bonn, Germany.
Peter BrossartDepartment of Internal Medicine III, University Hospital Bonn, Bonn, Germany.
Cornelius van BeekumDepartment of Visceral Surgery, University Hospital Bonn, Bonn, Germany.
Alexander SemaanDepartment of Visceral Surgery, University Hospital Bonn, Bonn, Germany.
Hanno MatthaeiDepartment of Visceral Surgery, University Hospital Bonn, Bonn, Germany.
Steffen ManekellerDepartment of Visceral Surgery, University Hospital Bonn, Bonn, Germany.
Alois M SprinkartDepartment of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany.
Sebastian NowakDepartment of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany.
Julian LuetkensDepartment of Diagnostic and Interventional Radiology, University Hospital Bonn, Bonn, Germany.
Jörg C KalffDepartment of Visceral Surgery, University Hospital Bonn, Bonn, Germany.
Christian P StrassburgDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany.
Maria A González-CarmonaDepartment of Internal Medicine I, University Hospital Bonn, Bonn, Germany. maria.gonzalez-carmona@ukbonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lenvatinib is a multiple receptor tyrosine kinase inhibitor (TKI) approved for first-line treatment of patients with unresectable hepatocellular carcinoma (HCC). TKI are suspected of exacerbating muscle loss in patients with cancer. In this study, we analyze the role of muscle loss in patients with advanced HCC treated with lenvatinib. This is a retrospective analysis of a real-life cohort of 25 patients with advanced HCC who were treated with lenvatinib from 2018 to March 2021 in Germany. Patients were stratified for loss of skeletal muscle area during the first three months of lenvatinib therapy. Overall survival (OS), progression-free survival (PFS) and toxicity were analyzed for all patients, especially regarding loss of muscle before and during the first three months of therapy with lenvatinib. Three months after beginning of therapy with lenvatinib, a significant reduction of muscle mass was observed in 60% of patients (p = 0.035). Despite increase of loss of skeletal muscle, patients benefitted from lenvatinib in our cohort of patients in terms of OS and PFS and did not experience increased toxicity. Furthermore, muscle loss was not a negative predictor of survival in the univariate analysis (p = 0.675). Patients with advanced hepatocellular carcinoma experience muscle loss with lenvatinib therapy. However, despite progressive muscle loss, patients benefit from a therapy with lenvatinib in terms of OS and PFS without increased toxicity. However, assessment and prophylaxis of skeletal muscle status should be recommended during a therapy with lenvatinib.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsPhenylurea CompoundsQuinolinesSarcopeniaAgedAged, 80 and overAntineoplastic AgentsFemaleHumansMaleMiddle AgedProgression-Free SurvivalProtein Kinase InhibitorsRetrospective StudiesAntineoplastic AgentslenvatinibPhenylurea CompoundsProtein Kinase InhibitorsQuinolines

Identifiers

PMID39333610
PMCPMC11437060

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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.