Changes in smoking behaviour are not modelled. | |
Programme uptake will be similar in real life to in the UKLS trial. | |
There is full concordance with screening programme (i.e. no missed appointments) | |
Health-related quality of life similar for preclinical and diagnosed lung cancer (stratified by stage). | |
Health-related quality of life similar for clinically presenting and screen-detected lung cancer of the same stage. | |
Health-related quality of life for diagnosed lung cancer is constant until death. | |
Natural history of lung cancers is similar across all included individuals. | |
Lung cancers progress through stages in numerical order without skipping any stages. | |
Sensitivity of LDCT is independent of patient and tumour characteristics. | |
Lung cancer mortality: screening cannot be less effective than no screening. | |
Mortality from preclinical lung cancer assumed to be negligible. | |
Lung cancer incidence in participating population similar to incidence in general smoking (current and former) population. | |
Survival in participating population similar to survival in general population (stratified by stage). | |
Incidental findings not modelled. | |
True-positive results lead to immediate diagnosis and treatment. | |
False-positive and indeterminate results are treated equivalently. | |
Non-attendance of screening was not explicitly modelled | |
Additional cancers caused by radiation exposure not modelled. | |
Risk prediction is dependent only on prevalence of occult lung cancer or short-term incidence (within 3 years). |