Evidence map›Paper›PMID 24577803›Full record

ArticleCancer2014

Comparative analysis of 5 lung cancer natural history and screening models that reproduce outcomes of the NLST and PLCO trials.

Rafael Meza, Kevin ten Haaf, Chung Yin Kong, Ayca Erdogan, William C Black, Martin C Tammemagi, Sung Eun Choi, Jihyoun Jeon, Summer S Han, Vidit Munshi and 7 more

Abstract readComparative Study
In one paragraph

Article in Cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 3 pooled it
–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

56 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. Guideline
  4. Lung cancer detectability by test, histology, stage, and gender: estimates from the NLST and the PLCO trials.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2015
    Trial
  5. Article
  6. Article
  7. Article
  8. A Scoping Review on Calibration Methods for Cancer Simulation Models.Medical decision making : an international journal of the Society for Medical Decision Making · 2025
    Article
  9. Article
  10. Natural history models for lung Cancer: A scoping review.Lung cancer (Amsterdam, Netherlands) · 2025
    Article
  11. Article
  12. The Impact of Model Assumptions on Personalized Lung Cancer Screening Recommendations.Medical decision making : an international journal of the Society for Medical Decision Making · 2024
    Article
  13. Lung cancer screening: where do we stand?Breathe (Sheffield, England) · 2024
    Review
  14. Article
  15. Article
  16. Birth Cohort‒Specific Smoking Patterns by Family Income in the U.S.American journal of preventive medicine · 2023
    Article
  17. Article
  18. Article
  19. Article
  20. 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

17 authors.

Rafael MezaDepartment of Epidemiology, University of Michigan, Ann Arbor, Michigan.
Kevin ten Haaf
Chung Yin Kong
Ayca Erdogan
William C Black
Martin C Tammemagi
Sung Eun Choi
Jihyoun Jeon
Summer S Han
Vidit Munshi
Joost van Rosmalen
Paul Pinsky
Pamela M McMahon
Harry J de Koning
Eric J Feuer
William D Hazelton
Sylvia K Plevritis

Funding

Comparative Modeling of Lung Cancer Control PoliciesU01CA152956 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DE KONING, HARRY J, KONG, CHUNG YIN · 2010 to 2014
$7.4M
NCI NIH HHS U01 CA152956NCI NIH HHS U01-CA152956
6 · The paper itself

Abstract

backgroundThe National Lung Screening Trial (NLST) demonstrated that low-dose computed tomography screening is an effective way of reducing lung cancer (LC) mortality. However, optimal screening strategies have not been determined to date and it is uncertain whether lighter smokers than those examined in the NLST may also benefit from screening. To address these questions, it is necessary to first develop LC natural history models that can reproduce NLST outcomes and simulate screening programs at the population level.

methodsFive independent LC screening models were developed using common inputs and calibration targets derived from the NLST and the Prostate, Lung, Colorectal and Ovarian Cancer Screening Trial (PLCO). Imputation of missing information regarding smoking, histology, and stage of disease for a small percentage of individuals and diagnosed LCs in both trials was performed. Models were calibrated to LC incidence, mortality, or both outcomes simultaneously.

resultsInitially, all models were calibrated to the NLST and validated against PLCO. Models were found to validate well against individuals in PLCO who would have been eligible for the NLST. However, all models required further calibration to PLCO to adequately capture LC outcomes in PLCO never-smokers and light smokers. Final versions of all models produced incidence and mortality outcomes in the presence and absence of screening that were consistent with both trials.

conclusionsThe authors developed 5 distinct LC screening simulation models based on the evidence in the NLST and PLCO. The results of their analyses demonstrated that the NLST and PLCO have produced consistent results. The resulting models can be important tools to generate additional evidence to determine the effectiveness of lung cancer screening strategies using low-dose computed tomography.

Indexed as

CalibrationClinical Trials as TopicEarly Detection of CancerFemaleHumansLung NeoplasmsMaleTomography, X-Ray ComputedCancer Intervention and Surveillance Modeling Network (CISNET)cancer natural history modelscomparative modeling analyseslow-dose CT screeninglung cancer screeningsimulation modelsmoking and lung cancer

Identifiers

PMID24577803
PMCPMC4031303

What OpenQuestion holds

Textmetadata
LicenceTDM
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.