Evidence map›Paper›PMID 40795838›Full record

ArticleThe oncologist2025

Real-world clinical outcomes of cabozantinib as a second-line treatment for advanced hepatocellular carcinoma: a retrospective US claims analysis.

Daniel H Ahn, Noh Jin Park, Michael Locker, Zheng-Yi Zhou, Xiaoyu Nie, Travis Wang, Shengsheng Yu

Abstract read
In one paragraph

Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Daniel H AhnDepartment of Medical Oncology, Mayo Clinic, Phoenix, AZ 85054, United States.
Noh Jin ParkDepartment of Medical Affairs, Exelixis, Inc., Alameda, CA 94502, United States.
Michael LockerDepartment of Medical Affairs, Exelixis, Inc., Alameda, CA 94502, United States.
Zheng-Yi ZhouAnalysis Group, Inc., Boston, MA 02199, United States.
Xiaoyu NieAnalysis Group, Inc., Boston, MA 02199, United States.
Travis WangAnalysis Group, Inc., Boston, MA 02199, United States.
Shengsheng YuDepartment of Medical Affairs, Exelixis, Inc., Alameda, CA 94502, United States.ORCID 0000-0002-1630-8224

Funding

AstraZenecaExelixis, Inc.
6 · The paper itself

Abstract

backgroundCabozantinib is indicated for hepatocellular carcinoma (HCC) following first-line (1L) sorafenib, but the 1L standard has shifted to immuno-oncology (IO)-based regimens. This study evaluated real-world outcomes among patients with advanced HCC receiving second-line (2L) cabozantinib following 1L therapies, including newer regimens. PATIENTS AND

methodsUS claims data were used to identify adults with advanced HCC initiating 2L cabozantinib monotherapy (index date). Patients were stratified into three 1L treatment cohorts: IO monotherapy/IO + IO combination therapy; IO + non-IO combination therapy; or tyrosine kinase inhibitor (TKI) monotherapy. Real-world time to treatment discontinuation (rwTTD), real-world time to next treatment or death (rwTNTD), real-world overall survival (rwOS), and cabozantinib dosing were assessed collectively and by cohort. Adverse events were assessed before/after cabozantinib initiation.

resultsAmong 148 patients who received 2L cabozantinib, 28 were in the IO monotherapy/IO + IO combination therapy cohort, 54 in the IO + non-IO combination therapy cohort, and 66 in the TKI monotherapy cohort. Median rwTTD among all patients was 3.2 months; median rwTNTD was 7.6 months; 12-month rwOS rate was 61.6%. There were no significant differences in these outcomes among the three cohorts. Overall, 44.6% of patients initiated 2L cabozantinib at 60 mg/day, of whom 39.4% required a dose reduction; 37.8% initiated at 40 mg/day, of whom 16.1% had a dose reduction. Adverse event rates were similar before/after cabozantinib initiation.

conclusionsCabozantinib shows consistent effectiveness and safety in the 2L HCC setting following prior TKIs or IO-based regimens in real-world clinical practice. These findings may inform 2L treatment decisions.

Indexed as

AnilidesCarcinoma, HepatocellularLiver NeoplasmsPyridinesAdultAgedFemaleHumansMaleMiddle AgedProtein Kinase InhibitorsRetrospective StudiesTreatment OutcomeUnited StatesAnilidescabozantinibProtein Kinase InhibitorsPyridinescabozantinibhepatocellular carcinomaretrospective studiestreatment outcome

Identifiers

PMID40795838
PMCPMC12445639

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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.