Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 May;263(2):578-83.
doi: 10.1148/radiol.12102489. Epub 2012 Mar 27.

Lung cancers diagnosed at annual CT screening: volume doubling times

Collaborators, Affiliations

Lung cancers diagnosed at annual CT screening: volume doubling times

Claudia I Henschke et al. Radiology. 2012 May.

Erratum in

  • Radiology. 2012 Jul;264(1):306

Abstract

Purpose: To empirically address the distribution of the volume doubling time (VDT) of lung cancers diagnosed in repeat annual rounds of computed tomographic (CT) screening in the International Early Lung Cancer Action Program (I-ELCAP), first and foremost with respect to rates of tumor growth but also in terms of cell types.

Materials and methods: All CT screenings in I-ELCAP from 1993 to 2009 were performed according to HIPAA-compliant protocols approved by the institutional review boards of the collaborating institutions. All instances of first diagnosis of primary lung cancer after a negative screening result 7-18 months earlier were identified, with symptom-prompted diagnoses included. Lesion diameter was calculated by using the measured length and width of each cancer at the time when the nodule was first identified for further work-up and at the time of the most recent prior screening, 7-18 months earlier. The length and width were measured a second time for each cancer, and the geometric mean of the two calculated diameters was used to calculate the VDT. The χ(2) statistic was used to compare the VDT distributions.

Results: The median VDT for 111 cancers was 98 days (interquartile range, 108). For 56 (50%) cancers it was less than 100 days, and for three (3%) cancers it was more than 400 days. Adenocarcinoma was the most frequent cell type (50%), followed by squamous cell carcinoma (19%), small cell carcinoma (19%), and others (12%). Lung cancers manifesting as subsolid nodules had significantly longer VDTs than those manifesting as solid nodules (P < .0001).

Conclusion: Lung cancers diagnosed in annual repeat rounds of CT screening, as manifest by the VDT and cell-type distributions, are similar to those diagnosed in the absence of screening.

PubMed Disclaimer

Figures

None
Graph shows cumulative frequency distribution of the calculated VDT, separately for cancers manifesting as solid (n = 99) and those manifesting as subsolid (n = 12) nodules.

Similar articles

Cited by

References

    1. Black WC. Computed tomography screening for lung cancer: review of screening principles and update on current status. Cancer 2007;110(11):2370–2384 - PubMed
    1. Bach PB. Overdiagnosis in lung cancer: different perspectives, definitions, implications. Thorax 2008;63(4):298–300 - PubMed
    1. Bach PB, Silvestri GA, Hanger M, Jett JR; American College of Chest Physicians. Screening for lung cancer: ACCP evidence-based clinical practice guidelines (2nd edition). Chest 2007;132(3 Suppl):69S–77S - PubMed
    1. Day NE, Walter SD, Collette B. Statistical models of disease natural history: their use in the evaluation of screening programmes. In: Prorok PC, Miller AB, eds. Screening for cancer. I. General on evaluation of screening for cancer and screening for lung, bladder, and oral cancer. UICC Technical Report Series No 78. Geneva, Switzerland: Union for International Cancer Control, 1984; 55–70
    1. Morrison A. Screening in chronic disease. New York, NY: Oxford University Press, 1992

Publication types