Evidence map›Paper›PMID 33140194›Full record

ArticleClinical drug investigation2020

Cost-Effectiveness of Lenvatinib Compared with Sorafenib for the First-Line Treatment of Advanced Hepatocellular Carcinoma in Australia.

Masnoon Saiyed, Joshua Byrnes, Tushar Srivastava, Paul Scuffham, Martin Downes

Abstract read
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In one paragraph

Article in Clinical drug investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 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

5 authors at 2 institutions in 2 countries.

Masnoon SaiyedCentre for Applied Health Economics, Griffith University, Nathan, QLD, 4111, Australia. m.saiyed@griffith.edu.au.ORCID http://orcid.org/0000-0002-6154-7021
Joshua ByrnesCentre for Applied Health Economics, Griffith University, Nathan, QLD, 4111, Australia.ORCID http://orcid.org/0000-0001-6562-711X
Tushar SrivastavaSchool of Health and Related Research (ScHARR), University of Sheffield, Sheffield, S1 4DA, UK.ORCID http://orcid.org/0000-0002-5961-9348
Paul ScuffhamCentre for Applied Health Economics, Griffith University, Nathan, QLD, 4111, Australia.ORCID http://orcid.org/0000-0001-5931-642X
Martin DownesCentre for Applied Health Economics, Griffith University, Nathan, QLD, 4111, Australia.ORCID http://orcid.org/0000-0003-3617-5307
Griffith University · AUUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveIn the REFLECT trial, lenvatinib showed superior clinical benefits to sorafenib in terms of progression-free survival and was non-inferior for overall survival in the treatment of advanced hepatocellular carcinoma (HCC). We assessed the cost-effectiveness of lenvatinib compared with sorafenib for patients with advanced HCC in Australia.

methodA partitioned-survival model was built to perform a cost-effectiveness analysis comparing lenvatinib and sorafenib from an Australian health-system perspective. Survival curves were obtained from the REFLECT trial and fitted with parametric survival functions for extrapolation purposes beyond the trial follow-up. Cost and quality-adjusted life-years (QALYs) were accrued over the 10-year time horizon of the model. Deterministic and probability sensitivity analysis (PSA) were carried out to verify the validity of the model.

resultsLenvatinib incurred higher costs (A$96,325) and superior health outcomes (QALYs: 1.205), while sorafenib had lower costs (A$92,394) and inferior health outcomes (QALYs: 1.086). Thus, lenvatinib yielded an incremental cost-utility ratio of A$33,028/QALY gained. Further, the results of the PSA found that the probability of lenvatinib being cost-effective at a willingness-to-pay threshold of A$50,000/QALY was 64%.

conclusionOur study found that, at current prices, lenvatinib is a cost-effective treatment option compared with sorafenib for the first-line treatment of patients with advanced HCC.

Indexed as

Antineoplastic AgentsAustraliaCarcinoma, HepatocellularCost-Benefit AnalysisFemaleHumansLiver NeoplasmsMalePhenylurea CompoundsQuality-Adjusted Life YearsQuinolinesSorafenibAntineoplastic AgentslenvatinibPhenylurea CompoundsQuinolinesSorafenib

Identifiers

PMID33140194
OpenAlexW3095699364

What OpenQuestion holds

Textmetadata
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.