Evidence map›Paper›PMID 32378799›Full record

ArticleCancer medicine2020

Second-line treatment of hepatocellular carcinoma after sorafenib: Characterizing treatments used over the past 10 years and real-world eligibility for cabozantinib, regorafenib, and ramucirumab.

Andrea S Fung, Vincent C Tam, Daniel E Meyers, Hao-Wen Sim, Jennifer J Knox, Valeriya Zaborska, Janine Davies, Yoo-Joung Ko, Eugene Batuyong, Haider Samawi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  7. Progression patterns and therapeutic sequencing following immune checkpoint inhibition for hepatocellular carcinoma: An international observational study.Liver international : official journal of the International Association for the Study of the Liver · 2023
    Observational
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  11. Observational
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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

12 authors at 6 institutions in 2 countries.

Andrea S FungTom Baker Cancer Centre, Calgary, AB, Canada.ORCID 0000-0002-2031-6921
Vincent C TamTom Baker Cancer Centre, Calgary, AB, Canada.
Daniel E MeyersTom Baker Cancer Centre, Calgary, AB, Canada.ORCID 0000-0002-7619-7327
Hao-Wen SimNHMRC Clinical Trials Centre, University of Sydney, Camperdown, NSW, Australia.
Jennifer J KnoxPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Valeriya ZaborskaBC Cancer Agency, Vancouver Centre, Vancouver, BC, Canada.
Janine DaviesBC Cancer Agency, Vancouver Centre, Vancouver, BC, Canada.
Yoo-Joung KoSunnybrook Health Sciences Centre - Odette Cancer Centre, Toronto, ON, Canada.
Eugene BatuyongTom Baker Cancer Centre, Calgary, AB, Canada.
Haider SamawiSt. Michael's Hospital, Toronto, ON, Canada.
Winson Y CheungTom Baker Cancer Centre, Calgary, AB, Canada.
Richard Lee-YingTom Baker Cancer Centre, Calgary, AB, Canada.ORCID 0000-0003-0913-6046
University of Calgary · CABC Cancer Agency · CAPrincess Margaret Cancer Centre · CASt. Michael's Hospital · CASunnybrook Health Science Centre · CAThe University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe CELESTIAL, RESORCE, and REACH-2 trials showed survival benefit of cabozantinib, regorafenib, and ramucirumab, respectively, in hepatocellular carcinoma (HCC) patients treated with sorafenib who had good performance status (ECOG 0-1) and liver function (Child-Pugh-A). This study characterizes subsequent treatments received by HCC patients after sorafenib, and determines the proportion of patients eligible for novel therapies if strict eligibility criteria (SEC) were utilized compared to more liberal modified eligibility criteria (MEC, including ECOG 2, Child-Pugh-B7).

methodsHCC patients who received sorafenib between 2008 and 2017 were included from the Canadian HCC CHORD Database. Patients were classified as eligible or ineligible based on available CELESTIAL, RESORCE, and REACH-2 trial SEC or MEC. Median overall survival (mOS) was assessed using the Kaplan-Meier method.

resultsA total of 730 patients were identified; and 172 (23.6%) received subsequent treatment. Patients who received subsequent treatment had longer mOS than those who did not (12.1 vs 3.3 months; P < .001). Using SEC, only 13.1% of patients would be eligible for cabozantinib, regorafenib, or ramucirumab. Expanding eligibility to include patients who meet MEC increased the proportion of eligible patients to 31.7%. Higher ineligibility for regorafenib and ramucirumab was driven by trial-specific criteria, including sorafenib intolerance (28%) for RESORCE and AFP <400 (58.9%) for REACH-2.

conclusionsA small proportion of real-world HCC patients would be eligible for cabozantinib, regorafenib, or ramucirumab if SEC in clinical trials were followed, while more than double would be eligible if MEC were applied. Patients who received subsequent treatment had improved mOS, regardless of whether they met SEC or MEC.

Indexed as

AnilidesAntibodies, Monoclonal, HumanizedAntineoplastic AgentsCanadaCarcinoma, HepatocellularClinical Trials, Phase III as TopicDatabases, FactualFemaleHumansKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedPatient SelectionPhenylurea CompoundsPyridinesAnilidesAntibodies, Monoclonal, HumanizedAntineoplastic AgentscabozantinibPhenylurea CompoundsPyridinesRamucirumabregorafenibSorafenibcabozantinibhepatocellular carcinomaramucirumabregorafenibtrial eligibility

Identifiers

PMID32378799
PMCPMC7333842
OpenAlexW3021210585

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.