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LDCT lung cancer screening in populations at different risk for lung cancer
INTRODUCTION: The improvement of low-dose CT (LDCT) lung cancer screening selection criteria could help to include more individuals who have lung cancer, or in whom lung cancer will develop, while avoiding significant cost increase. We evaluated baseline results of LDCT lung cancer screening in a po...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011883/ https://www.ncbi.nlm.nih.gov/pubmed/33371010 http://dx.doi.org/10.1136/bmjresp-2019-000455 |
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author | Teles, Gustavo Borges da Silva Macedo, Ana Carolina Sandoval Chate, Rodrigo Caruso Valente, Viviane Arevalo Tabone Funari, Marcelo Buarque de Gusmao Szarf, Gilberto |
author_facet | Teles, Gustavo Borges da Silva Macedo, Ana Carolina Sandoval Chate, Rodrigo Caruso Valente, Viviane Arevalo Tabone Funari, Marcelo Buarque de Gusmao Szarf, Gilberto |
author_sort | Teles, Gustavo Borges da Silva |
collection | PubMed |
description | INTRODUCTION: The improvement of low-dose CT (LDCT) lung cancer screening selection criteria could help to include more individuals who have lung cancer, or in whom lung cancer will develop, while avoiding significant cost increase. We evaluated baseline results of LDCT lung cancer screening in a population with a heterogeneous risk profile for lung cancer. METHODS: LDCT lung cancer screening was implemented alongside a preventive health programme in a private hospital in Brazil. Individuals older than 45 years, smokers and former smokers, regardless of tobacco exposure, were included. Patients were classified according to the National Lung Screening Trial (NLST) eligibility criteria and to PLCO(m2012) 6-year lung cancer risk. Patient characteristics, CT positivity rate, detection rate of lung cancer and false-positive rate were assessed. RESULTS: LDCT scans of 472 patients were evaluated and three lung adenocarcinomas were diagnosed. CT positivity rate (Lung-RADS 3/4) was significantly higher (p=0.019) in the NLST group (10.1% (95% CI, 5.9% to 16.9%)) than in the non-NLST group (3.6% (95% CI, 2.62% to 4.83%)) and in the PLCO(m2012) high-risk group (14.3% (95% CI, 6.8% to 27.7%)) than in the PLCO(m2012) low-risk group (3.7% (95% CI, 2.9% to 4.8%)) (p=0.016). Detection rate of lung cancer was also significantly higher (p=0.018) among PLCO(m2012) high-risk patients (5.7% (95% CI, 2.5% to 12.6%)) than in the PLCO(m2012) low-risk individuals (0.2% (95% CI, 0.1% to 1.1%)). The false-positive rate for NLST criteria (16.4% (95% CI, 13.2% to 20.1%)) was higher (p<0.001) than for PLCO(m2012) criteria (7.6 (95% CI, 5.3% to 10.5%)). DISCUSSION: Our study indicates a lower performance when screening low-risk individuals in comparison to screening patients meeting NLST criteria and PLCO(m2012) high-risk patients. Also, incorporating PLCO(m2012) 6-year lung cancer risk ≥0.0151 as an eligibility criterion seems to increase lung cancer screening effectiveness. |
format | Online Article Text |
id | pubmed-7011883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-70118832020-02-25 LDCT lung cancer screening in populations at different risk for lung cancer Teles, Gustavo Borges da Silva Macedo, Ana Carolina Sandoval Chate, Rodrigo Caruso Valente, Viviane Arevalo Tabone Funari, Marcelo Buarque de Gusmao Szarf, Gilberto BMJ Open Respir Res Lung Cancer INTRODUCTION: The improvement of low-dose CT (LDCT) lung cancer screening selection criteria could help to include more individuals who have lung cancer, or in whom lung cancer will develop, while avoiding significant cost increase. We evaluated baseline results of LDCT lung cancer screening in a population with a heterogeneous risk profile for lung cancer. METHODS: LDCT lung cancer screening was implemented alongside a preventive health programme in a private hospital in Brazil. Individuals older than 45 years, smokers and former smokers, regardless of tobacco exposure, were included. Patients were classified according to the National Lung Screening Trial (NLST) eligibility criteria and to PLCO(m2012) 6-year lung cancer risk. Patient characteristics, CT positivity rate, detection rate of lung cancer and false-positive rate were assessed. RESULTS: LDCT scans of 472 patients were evaluated and three lung adenocarcinomas were diagnosed. CT positivity rate (Lung-RADS 3/4) was significantly higher (p=0.019) in the NLST group (10.1% (95% CI, 5.9% to 16.9%)) than in the non-NLST group (3.6% (95% CI, 2.62% to 4.83%)) and in the PLCO(m2012) high-risk group (14.3% (95% CI, 6.8% to 27.7%)) than in the PLCO(m2012) low-risk group (3.7% (95% CI, 2.9% to 4.8%)) (p=0.016). Detection rate of lung cancer was also significantly higher (p=0.018) among PLCO(m2012) high-risk patients (5.7% (95% CI, 2.5% to 12.6%)) than in the PLCO(m2012) low-risk individuals (0.2% (95% CI, 0.1% to 1.1%)). The false-positive rate for NLST criteria (16.4% (95% CI, 13.2% to 20.1%)) was higher (p<0.001) than for PLCO(m2012) criteria (7.6 (95% CI, 5.3% to 10.5%)). DISCUSSION: Our study indicates a lower performance when screening low-risk individuals in comparison to screening patients meeting NLST criteria and PLCO(m2012) high-risk patients. Also, incorporating PLCO(m2012) 6-year lung cancer risk ≥0.0151 as an eligibility criterion seems to increase lung cancer screening effectiveness. BMJ Publishing Group 2020-02-06 /pmc/articles/PMC7011883/ /pubmed/33371010 http://dx.doi.org/10.1136/bmjresp-2019-000455 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Lung Cancer Teles, Gustavo Borges da Silva Macedo, Ana Carolina Sandoval Chate, Rodrigo Caruso Valente, Viviane Arevalo Tabone Funari, Marcelo Buarque de Gusmao Szarf, Gilberto LDCT lung cancer screening in populations at different risk for lung cancer |
title | LDCT lung cancer screening in populations at different risk for lung cancer |
title_full | LDCT lung cancer screening in populations at different risk for lung cancer |
title_fullStr | LDCT lung cancer screening in populations at different risk for lung cancer |
title_full_unstemmed | LDCT lung cancer screening in populations at different risk for lung cancer |
title_short | LDCT lung cancer screening in populations at different risk for lung cancer |
title_sort | ldct lung cancer screening in populations at different risk for lung cancer |
topic | Lung Cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011883/ https://www.ncbi.nlm.nih.gov/pubmed/33371010 http://dx.doi.org/10.1136/bmjresp-2019-000455 |
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