Evidence map›Paper›PMID 36358592›Full record

ArticleCancers2022

Cabozantinib Following Immunotherapy in Patients with Advanced Hepatocellular Carcinoma.

Michael H Storandt, Jennifer J Gile, Mathias E Palmer, Tyler J Zemla, Daniel H Ahn, Tanios S Bekaii-Saab, Zhaohui Jin, Nguyen H Tran, Amit Mahipal

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Michael H StorandtDepartment of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Jennifer J GileDepartment of Oncology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0001-6972-7986
Mathias E PalmerDepartment of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Tyler J ZemlaDepartment of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN 55905, USA.
Daniel H AhnDepartment of Hematology/Oncology, Mayo Clinic, Phoenix, AZ 85054, USA.
Tanios S Bekaii-SaabDepartment of Hematology/Oncology, Mayo Clinic, Phoenix, AZ 85054, USA.
Zhaohui JinDepartment of Oncology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0001-7844-5833
Nguyen H TranDepartment of Oncology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-6104-6489
Amit MahipalDepartment of Oncology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-1111-8333
Mayo Clinic in Arizona · USWinnMed · USMayo Clinic · USUniversity Hospitals Seidman Cancer Center · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI AKHILESH PANDEY · 1985 to 2026
$151.3M
Working to Eliminate Care Disparities in Liver Cancer in Southeast Asian Americans: Transportation and Other Social Determinants of Health.K23MD017217 · NIMHD · MAYO CLINIC ROCHESTER · PI Nguyen H Tran · 2022 to 2026
$818k
NCI NIH HHS P30 CA015083NIH HHS P30CA15083NIMHD NIH HHS K23 MD017217
6 · The paper itself

Abstract

(1) Background: Cabozantinib, a multikinase inhibitor, is approved by the Food and Drug Administration (FDA) for the treatment of advanced hepatocellular carcinoma (HCC) following progression on sorafenib. Recently, atezolizumab plus bevacizumab has been approved in the first line setting for advanced HCC and has become the new standard of care. Whether cabozantinib improves outcomes following progression on immunotherapy remains unknown. We describe the clinical outcomes following treatment with immunotherapy in patients with advanced HCC who received cabozantinib. (2) Methods: We conducted a multicentric, retrospective analysis of patients with advanced HCC diagnosed between 2010-2021 at Mayo Clinic in Minnesota, Arizona, and Florida who received cabozantinib. Median overall survival and progression free survival analyses were performed using the Kaplan-Meier method. Adverse events were determined using Common Terminology Criteria for Adverse Events (CTCAE). (3). Results: We identified 26 patients with advanced HCC who received cabozantinib following progression on immunotherapy. Median progression free survival on cabozantinib therapy was 2.1 months (95% CI: 1.3-3.9) and median overall survival from time of cabozantinib initiation was 7.7 months (95% CI: 5.3-14.9). (4) Conclusion: The optimal sequencing of therapy for patients with advanced HCC following progression on immunotherapy remains unknown. Our study demonstrates that patients may benefit from treatment with cabozantinib following progression on immunotherapy.

Indexed as

cabozantinibhepatocellular cancerimmunotherapy

Identifiers

PMID36358592
PMCPMC9657200
OpenAlexW4307327421

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.