Evidence map›Paper›PMID 37436697›Full record

ArticleJournal of the National Cancer Institute2023

Cost-effectiveness analysis of 7 treatments in metastatic hormone-sensitive prostate cancer: a public-payer perspective.

Minkyoung Yoo, Richard E Nelson, Benjamin Haaland, Maura Dougherty, Zachary A Cutshall, Rhea Kohli, Rylee Beckstead, Manish Kohli

Open access · bronzeAbstract readNetwork Meta-Analysis
In one paragraph

Article in Journal of the National Cancer Institute, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% 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, 2 syntheses or guidelines pooled it, 14 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

8 authors at 3 institutions in 1 country.

Minkyoung YooDivision of Epidemiology, Department of Internal Medicine, University of Utah (UT) School of Medicine, Salt Lake City, UT, USA.
Richard E NelsonDivision of Epidemiology, Department of Internal Medicine, University of Utah (UT) School of Medicine, Salt Lake City, UT, USA.
Benjamin HaalandDepartment of Population Health Sciences, University of UT, Salt Lake City, UT, USA.
Maura DoughertyDepartment of Economics, University of UT, Salt Lake City, UT, USA.
Zachary A CutshallUniversity of UT School of Medicine, Salt Lake City, UT, USA.
Rhea KohliCase Western Reserve University, Cleveland, OH, USA.
Rylee BecksteadSchool of Medicine, University of UT, Salt Lake City, UT, USA.
Manish KohliDivision of Oncology-Department of Medicine, University of UT/Huntsman Cancer Institute, Salt Lake City, UT, USA.ORCID 0000-0002-9735-6614
University of Utah · USCase Western Reserve University · USHuntsman Cancer Institute · US

Funding

CTSA UM1 Program at University of UtahUM1TR004409 · NCATS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI RACHEL HESS, Jennifer Juhl Majersik · 2023 to 2026
$21.9M
NCATS NIH HHS 1UM1TR004409-01NCATS NIH HHS UM1 TR004409NCI NIH HHS
6 · The paper itself

Abstract

backgroundRecently, several new treatment regimens have been approved for treating metastatic hormone-sensitive prostate cancer, building on androgen deprivation therapy alone. These include docetaxel androgen deprivation therapy, abiraterone acetate-prednisone androgen deprivation therapy, apalutamide androgen deprivation therapy, enzalutamide androgen deprivation therapy, darolutamide-docetaxel androgen deprivation therapy, and abiraterone-prednisone androgen deprivation therapy with docetaxel. There are no validated predictive biomarkers for choosing a specific regimen. The goal of this study was to conduct a health economic outcome evaluation to determine the optimal treatment from the US public sector (Veterans Affairs).

methodsWe developed a partitioned survival model in which metastatic hormone-sensitive prostate cancer patients transitioned between 3 health states (progression free, progressive disease to castrate resistance state, and death) at monthly intervals based on Weibull survival model estimated from published Kaplan-Meier curves using a Bayesian network meta-analysis of 7 clinical trials (7208 patients). The effectiveness outcome in our model was quality-adjusted life-years (QALYs). Cost input parameters included initial and subsequent treatment costs and costs for terminal care and for managing grade 3 or higher drug-related adverse events and were obtained from the Federal Supply Schedule and published literature.

resultsAverage 10-year costs ranged from $34 349 (androgen deprivation therapy) to $658 928 (darolutamide-docetaxel androgen deprivation therapy) and mean QALYs ranged from 3.25 (androgen deprivation therapy) to 4.57 (enzalutamide androgen deprivation therapy). Treatment strategies docetaxel androgen deprivation therapy, enzalutamide androgen deprivation therapy docetaxel, apalutamide androgen deprivation therapy, and darolutamide-docetaxel androgen deprivation therapy were eliminated because of dominance (ie, they were more costly and less effective than other strategies). Of the remaining strategies, abiraterone acetate-prednisone androgen deprivation therapy was the most cost-effective strategy at a willingness-to-pay threshold of $100 000/QALY (incremental cost-effectiveness ratios = $21 247/QALY).

conclusionsOur simulation model found abiraterone acetate-prednisone androgen deprivation therapy to be an optimal first-line treatment for metastatic hormone-sensitive prostate cancer from a public (Veterans Affairs) payer perspective.

Indexed as

Prostatic NeoplasmsProstatic Neoplasms, Castration-ResistantAbiraterone AcetateAndrogen AntagonistsAndrogensBayes TheoremBenzamidesCost-Effectiveness AnalysisDocetaxelHumansMaleNitrilesPhenylthiohydantoinPrednisoneTreatment OutcomeAbiraterone AcetateAndrogen AntagonistsAndrogensBenzamidesDocetaxelenzalutamideNitrilesPhenylthiohydantoinPrednisone

Identifiers

PMID37436697
PMCPMC10637034
OpenAlexW4383998267

What Socratic 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 Socratic graph.