Evidence map›Paper›PMID 36160737›Full record

ArticleWorld journal of gastrointestinal oncology2022

Second-line therapy for advanced hepatocellular carcinoma with regorafenib or cabozantinib: Multicenter French clinical experience in real-life after matching.

Xavier Adhoute, Marie De Matharel, Laurent Mineur, Guillaume Pénaranda, Dann Ouizeman, Clemence Toullec, Albert Tran, Paul Castellani, Armelle Rollet, Valérie Oules and 4 more

Abstract read
In one paragraph

Article in World journal of gastrointestinal oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. 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

14 authors.

Xavier AdhouteDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France. xvadhoute@gmail.com.
Marie De MatharelDepartment of Gastroenterology and Hepatology, Hôpital Universitaire de l'Archet, Nice 06000, France.
Laurent MineurDepartment of Oncology, Institut Sainte-Catherine, Avignon 84000, France.
Guillaume PénarandaDepartment of Biostatistics, AlphaBio Laboratory, Marseille 13000, France.
Dann OuizemanDepartment of Gastroenterology and Hepatology, Hôpital Universitaire de l'Archet, Nice 06000, France.
Clemence ToullecDepartment of Oncology, Institut Sainte-Catherine, Avignon 84000, France.
Albert TranDepartment of Gastroenterology and Hepatology, Hôpital Universitaire de l'Archet, Nice 06000, France.
Paul CastellaniDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France.
Armelle RolletDepartment of Oncology, Institut Sainte-Catherine, Avignon 84000, France.
Valérie OulesDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France.
Hervé PerrierDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France.
Si Nafa Si AhmedDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France.
Marc BourliereDepartment of Gastroenterology and Hepatology, Hôpital Saint-Joseph, Marseille 13000, France.
Rodolphe AntyDepartment of Gastroenterology and Hepatology, Hôpital Universitaire de l'Archet, Nice 06000, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStarting a second-line systemic treatment for hepatocellular carcinoma (HCC) is a common situation. The only therapeutic options in France are two broad-spectrum tyrosine kinase inhibitors (TKIs), regorafenib (REG) and cabozantinib (CBZ), but no comparative real-life studies are available.

aimTo evaluate the progression-free survival (PFS) of patients treated with REG or CBZ, we investigated the disease control rate (DCR), overall survival (OS), and safety of both drugs. To identify the variables associated with disease progression over time.

methodsA retrospective multicenter study was performed on the clinical data of patients attending one of three referral centers (Avignon, Marseille, and Nice) between January 2017 and March 2021 using propensity score matching. PFS and OS were assessed using the Kaplan-Meier method. Multivariate analysis (MA) of progression risk factors over time was performed in matched-pair groups.

resultsFifty-eight patients 68 (62-74) years old with HCC, Barcelona clinic liver cancer (BCLC) B/C (86%), Child-Pugh (CP)-A/B (24%) received REG for 3.4 (1.4-10.5) mo as second-line therapy. Twenty-eight patients 68 (60-73) years, BCLC B/C (75%), CP-A/B (25%) received CBZ for 3.7 (1.8-4.9) mo after first-line treatment with sorafenib [3 (2-4) (CBZ)

conclusionThis multicenter indirect comparative study found no significant difference in PFS between REG and CBZ as second-line therapy for advanced HCC. Elevated levels of inflammatory markers (CRP and NLR) and AST were associated with non-control of TKIs over time. A 2-mo online progression risk calculation is proposed.

Indexed as

CabozantinibC-reactive proteinHepatocellular carcinomaNeutrophil-lymphocyte ratioRegorafenib

Identifiers

PMID36160737
PMCPMC9412937

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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.