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. 2014;3(6):491-498.
doi: 10.2217/LMT.14.41.

Assessing the benefits and harms of low-dose computed tomography screening for lung cancer

Affiliations

Assessing the benefits and harms of low-dose computed tomography screening for lung cancer

Paul F Pinsky. Lung Cancer Manag. 2014.

Abstract

The concept of using low-dose computed tomography (LDCT) for lung cancer screening goes back almost 25 years. In 2011, the National Lung Screening Trial (NLST) reported that LDCT screening significantly reduced mortality from lung cancer in a high risk population. This article evaluates the benefits and harms of LDCT screening, based largely on evidence from randomized trials. Harms include false-positive screens and resultant diagnostic procedures, overdiagnosed cancers, and radiation exposure. Benefits can be expressed as the number needed to be screened to prevent one lung cancer death or as estimated overall reductions in lung cancer mortality assuming LDCT population screening as recommended by guidelines. Indirect metrics of benefit, such as lung cancer survival and stage distribution, as well as measures of harms, will be important to monitor in the future as LDCT screening disseminates in the population.

Keywords: benefits; harms; low-dose CT; lung cancer; screening.

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Conflict of interest statement

Financial & competing interests disclosure

The author has no relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript.

No writing assistance was utilized in the production of this manuscript.

Figures

Figure 1
Figure 1. Schematic of benefits versus harms of low-dose CT screening
Outcomes for 1000 subjects scheduled for three annual rounds of low-dose CT screening. Derived from the experience of the National Lung Screening Trial. Note “screen-detected cancer” row excludes screen-detected cancers that were overdiagnosed and screen-detected cancers where lung cancer death was prevented. Subjects with a false-positive screen and a subsequent screen-detected cancer at a later screening round are grouped with the screen-detected cancers.

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