Evidence map›Paper›PMID 38239279›Full record

ArticleJournal of hepatocellular carcinoma2024

First-Line Treatment for Advanced Hepatocellular Carcinoma: A Three-Armed Real-World Comparison.

Robert Mahn, Oscar André Glüer, Farsaneh Sadeghlar, Christian Möhring, Taotao Zhou, Thomas Anhalt, Malte Benedikt Monin, Alexander Kania, Tim R Glowka, Georg Feldmann and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of hepatocellular carcinoma, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Pooled it
  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

15 authors at 1 institution in 1 country.

Robert Mahn *Department of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Oscar André Glüer *Department of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.ORCID 0009-0008-8309-1783
Farsaneh SadeghlarDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Christian MöhringDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.ORCID 0000-0001-7651-4401
Taotao ZhouDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Thomas AnhaltDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Malte Benedikt MoninDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Alexander KaniaDepartment of Surgery, University Hospital of Bonn, Bonn, Germany.
Tim R GlowkaDepartment of Surgery, University Hospital of Bonn, Bonn, Germany.
Georg FeldmannDepartment of Internal Medicine III, University Hospital of Bonn, Bonn, Germany.
Peter BrossartDepartment of Internal Medicine III, University Hospital of Bonn, Bonn, Germany.
Joerg C KalffDepartment of Surgery, University Hospital of Bonn, Bonn, Germany.
Ingo G H Schmidt-WolfDepartment of Integrated Oncology CIO Bonn, University Hospital of Bonn, Bonn, Germany.
Christian P StrassburgDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
Maria A Gonzalez-CarmonaDepartment of Internal Medicine I, University Hospital of Bonn, Bonn, Germany.
University Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: There are several existing systemic 1st- line therapies for advanced hepatocellular carcinoma (HCC), including atezolizumab/bevacizumab (Atez/Bev), sorafenib and lenvatinib. This study aims to compare the effectiveness of these three 1st-line systemic treatments in a real-world setting for HCC, focusing on specific patient subgroups analysis. Methods: A total of 177 patients with advanced HCC treated with Atez/Bev (n = 38), lenvatinib (n = 21) or sorafenib (n = 118) as 1st line systemic therapy were retrospectively analyzed and compared. Primary endpoints included objective response rate (ORR), progression-free survival (PFS) and 15-month overall survival (15-mo OS). Subgroups regarding liver function, etiology, previous therapy and toxicity were analyzed. Results: Atez/Bev demonstrated significantly longer median 15-month OS with 15.03 months compared to sorafenib with 9.43 months (p = 0.04) and lenvatinib with 8.93 months (p = 0.05). Similarly, it had highest ORR of 31.6% and longest median PFS with 7.97 months, independent of etiology. However, significantly superiority was observed only compared to sorafenib (ORR: 4.2% (p < 0.001); PFS: 4.57 months (p = 0.03)), but not comparing to lenvatinib (ORR: 28.6% (p = 0.87); PFS: 3.77 months (p = 0.10)). Atez/Bev also resulted in the longest PFS in patients with Child-Pugh A and ALBI 1 score and interestingly in those previously treated with SIRT. Contrary, sorafenib was non inferior in patients with impaired liver function. Conclusion: Atez/Bev achieved longest median PFS and 15-mo OS independent of etiology and particularly in patients with stable liver function or prior SIRT treatment. Regarding therapy response lenvatinib was non-inferior to Atez/Bev. Finally, sorafenib seemed to perform best for patients with deteriorated liver function.

Indexed as

first-line therapyHCCsubgroups

Identifiers

PMID38239279
PMCPMC10794153
OpenAlexW4390825505

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.