Trial reportBritish journal of cancer2013
Parameter estimates for invasive breast cancer progression in the Canadian National Breast Screening Study.
Trial report in British journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06193707 (Assessment of the Effect of Intelligence Remote Intervention on High-Risk Populations for Breast Cancer), which is not on this map. Cited by 9 papers, 1 of them a synthesis that pooled it.
What it found
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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.
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.
Assessment of the Effect of Intelligence Remote Intervention on High-Risk Populations for Breast Cancer
Who cites it
9 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Pooled it
- Is mammography screening beneficial: An individual-based stochastic model for breast cancer incidence and mortality.PLoS computational biology · 2020Trial
- Radiotherapy as a surgical alternative in ductal carcinoma in situ (DCIS): long-term survival benefits and predictors of invasive progression risk.Gland surgery · 2025Article
- Article
- Estimating Age-Specific Mean Sojourn Time of Breast Cancer and Sensitivity of Mammographic Screening by Breast Density among Korean Women.Cancer research and treatment · 2023Article
- Association between breast nodules, anxiety, depression and metabolic risk factors in a Chinese cohort.Frontiers in psychiatry · 2023Article
- Multistate models for the natural history of cancer progression.British journal of cancer · 2022Article
- Estimating Distributions of Breast Cancer Onset and Growth in a Swedish Mammography Screening Cohort.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2022Article
- Initiators and promoters for the occurrence of screen-detected breast cancer and the progression to clinically-detected interval breast cancer.Journal of epidemiology · 2017Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
backgroundThe aim of screening is to detect a cancer in the preclinical state. However, a false-positive or a false-negative test result is a real possibility.
methodsWe describe invasive breast cancer progression in the Canadian National Breast Screening Study and construct progression models with and without covariates. The effect of risk factors on transition intensities and false-negative probability is investigated. We estimate the transition rates, the sojourn time and sensitivity of diagnostic tests for women aged 40-49 and 50-59.
resultsAlthough younger women have a slower transition rate from healthy state to preclinical, their screen-detected tumour becomes evident sooner. Women aged 50-59 have a higher mortality rate compared with younger women. The mean sojourn times for women aged 40-49 and 50-59 are 2.5 years (95% CI: 1.7, 3.8) and 3.0 years (95% CI: 2.1, 4.3), respectively. Sensitivity of diagnostic procedures for older women is estimated to be 0.75 (95% CI: 0.55, 0.88), while women aged 40-49 have a lower sensitivity (0.61, 95% CI: 0.42, 0.77). Age is the only factor that affects the false-negative probability. For women aged 40-49, 'age at entry', 'history of breast disease' and 'families with breast cancer' are found to be significant for some of the transition rates. For the age-group 50-59, 'age at entry', 'history of breast disease', 'menstruation length' and 'number of live births' are found to affect the transition rates.
conclusionModelling and estimating the parameters of cancer progression are essential steps towards evaluating the effectiveness of screening policies. The parameters include the transition rates, the preclinical sojourn time, the sensitivity, and the effect of different risk factors on cancer progression.
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Registered trials
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