Performance of various risk prediction models in a large lung cancer screening cohort in Gdańsk, Poland-a comparative study.

Lung cancer low-dose computed tomography risk prediction models screening

Journal

Translational lung cancer research
ISSN: 2218-6751
Titre abrégé: Transl Lung Cancer Res
Pays: China
ID NLM: 101646875

Informations de publication

Date de publication:
Feb 2021
Historique:
entrez: 15 3 2021
pubmed: 16 3 2021
medline: 16 3 2021
Statut: ppublish

Résumé

Optimal selection criteria for the lung cancer screening programme remain a matter of an open debate. We performed a validation study of the three most promising lung cancer risk prediction models in a large lung cancer screening cohort of 6,631 individuals from a single European centre. A total of 6,631 healthy volunteers (aged 50-79, smoking history ≥30 pack-years) were enrolled in the MOLTEST BIS programme between 2016 and 2018. Each participant underwent a low-dose computed chest tomography scan, and selected participants underwent a further diagnostic work-up. Various lung cancer prediction models were applied to the recruited screenees, i.e., (I) Tammemagi's Prostate, Colorectal, and Ovarian Cancer Screening Trial 2012 (PLCO Lung cancer was diagnosed in 154 (2.3%) participants. Based on the risk estimates by PLCO Lung cancer screening enrollment based on the risk prediction models is superior to NCCN Group 1 selection criteria and offers a clinically significant reduction of screenees with a comparable proportion of detected lung cancer cases. Tammemagi's risk prediction model reduces the proportion of patients eligible for inclusion to a screening programme with a minimal loss of detected lung cancer cases.

Sections du résumé

BACKGROUND BACKGROUND
Optimal selection criteria for the lung cancer screening programme remain a matter of an open debate. We performed a validation study of the three most promising lung cancer risk prediction models in a large lung cancer screening cohort of 6,631 individuals from a single European centre.
METHODS METHODS
A total of 6,631 healthy volunteers (aged 50-79, smoking history ≥30 pack-years) were enrolled in the MOLTEST BIS programme between 2016 and 2018. Each participant underwent a low-dose computed chest tomography scan, and selected participants underwent a further diagnostic work-up. Various lung cancer prediction models were applied to the recruited screenees, i.e., (I) Tammemagi's Prostate, Colorectal, and Ovarian Cancer Screening Trial 2012 (PLCO
RESULTS RESULTS
Lung cancer was diagnosed in 154 (2.3%) participants. Based on the risk estimates by PLCO
CONCLUSIONS CONCLUSIONS
Lung cancer screening enrollment based on the risk prediction models is superior to NCCN Group 1 selection criteria and offers a clinically significant reduction of screenees with a comparable proportion of detected lung cancer cases. Tammemagi's risk prediction model reduces the proportion of patients eligible for inclusion to a screening programme with a minimal loss of detected lung cancer cases.

Identifiants

pubmed: 33718046
doi: 10.21037/tlcr-20-753
pii: tlcr-10-02-1083
pmc: PMC7947399
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1083-1090

Informations de copyright

2021 Translational Lung Cancer Research. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tlcr-20-753). The series “Implementation of CT-based screening of lung cancer” was commissioned by the editorial office without any funding or sponsorship. WR served as the unpaid Guest Editor of the series. TM reports personal fees from Roche/Genentech, outside the submitted work. The authors have no other conflicts of interest to declare.

Références

N Engl J Med. 2013 May 23;368(21):1980-91
pubmed: 23697514
J Natl Cancer Inst. 2003 Mar 19;95(6):470-8
pubmed: 12644540
PLoS Med. 2017 Apr 4;14(4):e1002277
pubmed: 28376113
N Engl J Med. 2013 Feb 21;368(8):728-36
pubmed: 23425165
Thorax. 2011 Apr;66(4):308-13
pubmed: 21317179
Cancer Prev Res (Phila). 2015 Jun;8(6):570-5
pubmed: 25873368
Interact Cardiovasc Thorac Surg. 2019 Mar 18;:
pubmed: 30887048
Radiology. 1982 Apr;143(1):29-36
pubmed: 7063747
Pol Arch Med Wewn. 2015;125(4):232-9
pubmed: 25764248
Br J Cancer. 2008 Jan 29;98(2):270-6
pubmed: 18087271
N Engl J Med. 2011 Aug 4;365(5):395-409
pubmed: 21714641
Ann Transl Med. 2017 Oct;5(20):406
pubmed: 29152506
J Thorac Imaging. 2015 Mar;30(2):88-100
pubmed: 25692785
Ann Transl Med. 2016 Apr;4(8):151
pubmed: 27195269
Int J Cancer. 2011 Oct 15;129(8):1907-13
pubmed: 21140453
Lung Cancer. 2016 Sep;99:46-52
pubmed: 27565913
Am J Respir Crit Care Med. 2015 Apr 15;191(8):924-31
pubmed: 25668622

Auteurs

Marcin Ostrowski (M)

Department of Thoracic Surgery, Medical University of Gdańsk, Gdańsk, Poland.

Franciszek Bińczyk (F)

Faculty of Automatic Control, Electronics and Computer Science, Silesian University of Technology, Gliwice, Poland.

Tomasz Marjański (T)

Department of Thoracic Surgery, Medical University of Gdańsk, Gdańsk, Poland.

Robert Dziedzic (R)

Department of Thoracic Surgery, Medical University of Gdańsk, Gdańsk, Poland.

Sylwia Pisiak (S)

Department of Non-Invasive Cardiac Diagnostics, Medical University of Gdańsk, Gdańsk, Poland.

Sylwia Małgorzewicz (S)

Department of Clinical Nutrition and Dietetics, Medical University of Gdańsk, Gdańsk, Poland.

Mariusz Adamek (M)

Department of Thoracic Surgery, Medical University of Silesia, Katowice, Poland.

Joanna Polańska (J)

Faculty of Automatic Control, Electronics and Computer Science, Silesian University of Technology, Gliwice, Poland.

Witold Rzyman (W)

Department of Thoracic Surgery, Medical University of Gdańsk, Gdańsk, Poland.

Classifications MeSH