Evidence map›Paper›PMID 37740609›Full record

ArticleCancer medicine2023

Economic evaluation of prostate cancer risk assessment methods: A cost-effectiveness analysis using population data.

Tima Mohammadi, Daphne P Guh, Alexander C T Tam, Reka E Pataky, Peter C Black, Alan So, Larry D Lynd, Wei Zhang, Annalijn I Conklin

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Overdiagnosis and Overtreatment in Prostate Cancer.Diseases (Basel, Switzerland) · 2025
    Review
  3. 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

9 authors at 3 institutions in 1 country.

Tima MohammadiCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Daphne P GuhCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Alexander C T TamCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.ORCID 0000-0002-3359-5552
Reka E PatakyCanadian Centre for Applied Research in Cancer Control, BC Cancer, Vancouver, British Columbia, Canada.
Peter C BlackDepartment of Urologic Sciences, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Alan SoDepartment of Urologic Sciences, Faculty of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Larry D LyndCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Wei ZhangCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Annalijn I ConklinCentre for Advancing Health Outcomes (formerly Centre for Health Evaluation and Outcome Sciences), Providence Health Care Research Institute, St. Paul's Hospital, Vancouver, British Columbia, Canada.
Providence Health Care · CAUniversity of British Columbia · CACanadian Centre for Applied Research in Cancer Control · CA

Funding

CIHR
6 · The paper itself

Abstract

backgroundThe current prostate cancer (PCa) screening standard of care (SOC) leads to unnecessary biopsies and overtreatment because decisions are guided by prostate-specific antigen (PSA) levels, which have low specificity in the gray zone (3-10 ng/mL). New risk assessment tools (RATs) aim to improve biopsy decision-making. We constructed a modeling framework to assess new RATs in men with gray zone PSA from the British Columbia healthcare system's perspective.

methodsWe evaluated the cost-effectiveness of a new RAT used in biopsy-naïve men aged 50+ with a PSA of 3-10 ng/mL using a time-dependent state-transition model. The model was informed by engaging patient partners and using linked administrative health data, supplemented with published literature. The incremental cost-effectiveness ratio and the probability of the RAT being cost-effective were calculated. Probabilistic analysis was used to assess parameter uncertainty.

resultsIn the base case, a RAT based on an existing biomarker's characteristics was a dominant strategy associated with a cost savings of $44 and a quality-adjusted life years (QALY) gain of 0.00253 over 18 years of follow-up. At a cost-effectiveness threshold of $50,000/QALY, the probability that using a RAT is cost-effective relative to the SOC was 73%. Outcomes were sensitive to RAT costs and accuracy, especially the detection rate of high-grade PCa. Results were also impacted by PCa prevalence and assumptions about undetected PCa survival.

conclusionsOur findings showed that a more accurate RAT to guide biopsy can be cost-effective. Our proposed general model can be used to analyze the cost-effectiveness of any novel RAT.

Indexed as

Prostate-Specific AntigenProstatic NeoplasmsCost-Benefit AnalysisCost-Effectiveness AnalysisHumansMaleRisk AssessmentProstate-Specific Antigeneconomic evaluationhealth administrative dataprostate cancerscreening

Identifiers

PMID37740609
PMCPMC10587968
OpenAlexW4386979873

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.