Evidence map›Paper›PMID 36006547›Full record

ArticleHepatology international2022

Lenvatinib for the treatment of hepatocellular carcinoma-a real-world multicenter Australian cohort study.

Kurvi Patwala, David Stephen Prince, Yael Celermajer, Waafiqa Alam, Eldho Paul, Simone Irene Strasser, Geoffrey William McCaughan, Paul Gow, Siddharth Sood, Elise Murphy and 17 more

Abstract readMulticenter Study
In one paragraph

Article in Hepatology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

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

  1. Pooled it
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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

27 authors.

Kurvi Patwala *Department of Gastroenterology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia. kurvipatwala@gmail.com.ORCID http://orcid.org/0000-0002-9235-146X
David Stephen Prince *AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown, NSW, 2050, Australia. David.Prince@health.nsw.gov.au.
Yael CelermajerAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown, NSW, 2050, Australia.
Waafiqa AlamDepartment of Gastroenterology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia.
Eldho PaulDepartment of Medicine, Monash University, Wellington Road, Clayton, VIC, 3800, Australia.
Simone Irene StrasserAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown, NSW, 2050, Australia.
Geoffrey William McCaughanAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown, NSW, 2050, Australia.
Paul GowDepartment of Gastroenterology and Liver Transplant, Austin Health, 145 Studley Road, Heidelberg, VIC, 3084, Australia.
Siddharth SoodDepartment of Gastroenterology, Royal Melbourne Hospital, 300 Grattan Street, Parkville, VIC, 3050, Australia.
Elise MurphyDepartment of Gastroenterology, Royal Melbourne Hospital, 300 Grattan Street, Parkville, VIC, 3050, Australia.
Stuart RobertsDepartment of Medicine, Monash University, Wellington Road, Clayton, VIC, 3800, Australia.
Elliot FreemanDepartment of Gastroenterology, Alfred Health, 55 Commercial Road, Melbourne, VIC, 3004, Australia.
Elizabeth StrattonDepartment of Gastroenterology, Liverpool Hospital, 75 Elizabeth Street, Liverpool, NSW, 2170, Australia.
Scott Anthony DavisonDepartment of Gastroenterology, Liverpool Hospital, 75 Elizabeth Street, Liverpool, NSW, 2170, Australia.
Miriam Tania LevyDepartment of Gastroenterology, Liverpool Hospital, 75 Elizabeth Street, Liverpool, NSW, 2170, Australia.
McCawley Clark-DicksonDepartment of Gastroenterology, Royal North Shore Hospital, Reserve Road, St Leonard's, NSW, 2065, Australia.
Vi NguyenDepartment of Gastroenterology, Royal North Shore Hospital, Reserve Road, St Leonard's, NSW, 2065, Australia.
Sally BellDepartment of Gastroenterology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia.
Amanda NicollDepartment of Gastroenterology, Eastern Health, 8 Arnold Street, Box Hill, VIC, 3128, Australia.
Ashley BloomDepartment of Gastroenterology, Eastern Health, 8 Arnold Street, Box Hill, VIC, 3128, Australia.
Alice Unah LeeDepartment of Gastroenterology, Concord Repatriation General Hospital, Hospital Road, Concord, NSW, 2139, Australia.
Marno RyanDepartment of Gastroenterology, St Vincent's Hospital, 41 Victoria Parade, Fitzroy, VIC, 3065, Australia.
Jessica HowellDepartment of Gastroenterology, St Vincent's Hospital, 41 Victoria Parade, Fitzroy, VIC, 3065, Australia.
Zina ValaydonDepartment of Gastroenterology, Western Health, 160 Gordon Street, Footscray, VIC, 3011, Australia.
Alexandra MackDepartment of Gastroenterology, Western Health, 160 Gordon Street, Footscray, VIC, 3011, Australia.
Ken LiuAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, 50 Missenden Road, Camperdown, NSW, 2050, Australia.
Anouk DevDepartment of Gastroenterology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHepatocellular carcinoma (HCC) is a serious complication of chronic liver disease. Lenvatinib is an oral multikinase inhibitor registered to treat advanced HCC. This study evaluates the real-world experience with lenvatinib in Australia.

methodsWe conducted a retrospective cohort study of patients treated with lenvatinib for advanced HCC between July 2018 and November 2020 at 11 Australian tertiary care hospitals. Baseline demographic data, tumor characteristics, lenvatinib dosing, adverse events (AEs) and clinical outcomes were collected. Overall survival (OS) was the primary outcome. Progression free survival (PFS) and AEs were secondary outcomes.

resultsA total of 155 patients were included and were predominantly male (90.7%) with a median age of 65 years (interquartile range [IQR]: 59-75). The main causes of chronic liver disease were hepatitis C infection (40.0%) and alcohol-related liver disease (34.2). Median OS and PFS were 7.7 (95% confidence interval [CI]: 5.8-14.0) and 5.3 months (95% CI: 2.8-9.2) respectively. Multivariate predictors of mortality were the need for dose reduction due to AEs (Hazard ratio [HR] 0.41, p < 0.01), new or worsening hypertension (HR 0.42, p < 0.01), diarrhoea (HR 0.47, p = 0.04) and more advanced BCLC stage (HR 2.50, p = 0.04). Multivariable predictors of disease progression were higher Child-Pugh score (HR 1.25, p = 0.04), the need for a dose reduction (HR 0.45, p < 0.01) and age (HR 0.96, p < 0.001). AEs occurred in 83.9% of patients with most being mild (71.6%).

conclusionsLenvatinib remains safe and effective in real-world use. Treatment emergent diarrhoea and hypertension, and the need for dose reduction appear to predict better OS.

Indexed as

Carcinoma, HepatocellularHypertensionLiver NeoplasmsQuinolinesAgedAustraliaCohort StudiesDiarrheaFemaleHumansMalePhenylurea CompoundsRetrospective StudieslenvatinibPhenylurea CompoundsQuinolinesAdverse effectsAustraliaChronic liver diseaseCohortDiarrhoeaHypertensionLiver malignancyMultikinase inhibitorOral therapySystemic therapy

Identifiers

PMID36006547
PMCPMC9525325

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Registered trials

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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.