Evidence map›Paper›PMID 20434974›Full record

ArticleCancer epidemiology2010

Estimating key parameters in periodic breast cancer screening-application to the Canadian National Breast Screening Study data.

Yinlu Chen, Guy Brock, Dongfeng Wu

Abstract read
In one paragraph

Article in Cancer epidemiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–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

6 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Article
  5. Article
  6. How does early detection by screening affect disease progression? Modeling estimated benefits in prostate cancer screening.Medical decision making : an international journal of the Society for Medical Decision Making
    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

3 authors.

Yinlu ChenDepartment of Bioinformatics and Biostatistics, School of Public Health and Informatics Science, University of Louisville, Louisville, KY 40202, USA.
Guy Brock
Dongfeng Wu

Funding

ZEBRAFISH VISUAL FUNCTION RECOVERY FOLLOWING OPTIC NERVE DAMAGEP20RR016481 · NCRR · UNIVERSITY OF LOUISVILLE · PI BARTON, HAZEL A · 2001 to 2011
$34.8M
Strategic Vision & Impact on Environmental HealthP30ES014443 · NIEHS · UNIVERSITY OF LOUISVILLE · PI PROUGH, RUSSELL ALLEN · 2007 to 2010
$4.4M
Transcriptional Coactivators and Pregnancy OutcomesR01HD053509 · NICHD · UNIVERSITY OF LOUISVILLE · PI GREENE, ROBERT M · 2008 to 2012
$1.5M
NUTRITIONAL EPIGENETICS AND OROFACIAL DEVELOPMENTR01DE018215 · NIDCR · UNIVERSITY OF LOUISVILLE · PI GREENE, ROBERT M · 2008 to 2011
$1.3M
Statistical Inference for Lead Time in Cancer ScreeningR03CA115012 · NCI · MISSISSIPPI STATE UNIVERSITY · PI WU, DONGFENG · 2005 to 2006
$136k
NCI NIH HHS R03 CA115012NCI NIH HHS R03CA115012NCRR NIH HHS P20 RR016481NCRR NIH HHS P20RR16481NICHD NIH HHS R01 HD053509NICHD NIH HHS R01-HD053509NIDCR NIH HHS P20-RR/DE177702NIDCR NIH HHS R01 DE018215NIDCR NIH HHS R01DE018215NIEHS NIH HHS P30 ES014443NIEHS NIH HHS P30-ES014443
6 · The paper itself

Abstract

problem statementBreast cancer screening in women of younger age has been controversial. The screening sensitivities, transition probabilities and sojourn time distributions are estimated for females aged 40-49 years and 50-59 years separately, using the Canadian National Breast Screening Study (CNBSS) data. The purpose is to estimate the lead time distribution and the probability of not detecting the cancer early. APPROACH: Within the 40-49-year-old and 50-59-year-old cohorts separately, the age-independent statistical model was applied. Bayesian estimators along with 95% highest probability density (HPD) credible intervals (CI) were calculated. Bayesian hypothesis testing was used to compare the parameter estimates of the two cohorts. The lead time density was also estimated for both the 40-49 and 50-59-year-old cohorts.

resultsThe screening sensitivity, transition probability of the disease, and mean sojourn time were all found to increase with age. For the 40-49-year-old and 50-59-year-old cohorts, the posterior mean sensitivities were 0.70 (95% HPD-CI: 0.46, 0.93) and 0.77 (0.61, 0.93), respectively. The posterior mean transition probabilities were 0.0023 (0.0018, 0.0027) and 0.0031 (0.0024, 0.0038), while the posterior mean sojourn times were 2.55 (1.56, 4.26) years and 3.15 (2.12, 4.96) years. Bayes factors for the ratio of posterior probabilities that the respective parameter was larger vs. smaller in the 50-59-year-old cohort were estimated to be 2.09, 40.8 and 3.0 for the sensitivity, transition probability, and mean sojourn time, respectively. All three Bayes factors were larger than two, indicating greater than 2:1 odds in favor of the hypothesis that each of these parameters was greater in the 50-59-year-old cohort. The estimated mean lead times were 0.83 years and 0.96 years if the two cohorts were screened annually.

conclusionsThe increase in sensitivity corresponds to an increase in the mean sojourn time. Breast cancer in younger women is more difficult to detect by screening tests and is more aggressive than breast cancer in older women. Women aged 50-59 tend to benefit more from screening compared with women aged 40-49.

Indexed as

Early Detection of CancerMammographyMass ScreeningModels, StatisticalAdultBayes TheoremBreast NeoplasmsCanadaFemaleHumansMiddle AgedRisk FactorsSurvival Rate

Identifiers

PMID20434974
PMCPMC2910214

What OpenQuestion holds

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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.