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Lung Cancer ScreeningLUCAS-LATAMNCT07524803

Lung Cancer Screening for Early Detection of Suspicious Lung Nodules in Latin America(LUCAS-LATAM)

An observational study of Lung Cancer Screening, run by Latin American Consortium for the Lung Cancer Research at 2 sites in 2 countries.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

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Trial summary

Prospective study to assess lung cancer screening with low dose CT scan (LDCT) in Latin America (LATAM) and prospectively evaluate chest-XRay analyzed with artificial intelligence (AI) using qXRin (QURE ai) at the initial visit correlating with the findins of the initial LDCT in patients with other high risk criteria… Read more about this study

Who is it for?
Ages 50 years and olderHealthy volunteers can take part
Conditions the study is for
Lung Cancer Screening
What is being tested?
Chest X-Ray, Low Dose CT scan
How many people
2,000 participants
Where
2 sitesin 2 countries
Study dates
1 May 2026to 1 May 2032
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: 2000 patients will be recruited in 4 Latin American countries (Mexico 700 pts,Costa Rica 300 pts, Colombia 500 pts, Argentina 500 pts)

Who may be able to join

  • 1. Men and women ≥50 years of age and one of any of the following criteria:
  • Exposure to wood smoke (at least 100 hours per year)
  • A family history of lung cancer in first-degree relatives
  • A diagnosis of COPD and/or emphysema
  • Smokers with a tobacco index of 10 years or more

Who cannot join

  • Lung cancer diagnosis or any other type of active cancer during the 5 years prior to the screening
  • Incomplete clinical information
  • Loss of 10% of the baseline weight during 6 months prior to study entry
  • Having a functional status, psychiatric condition or comorbidity that precludes curative treatment
  • Any situation that makes the subject ineligible for LDCT
  • Life expectancy ≤5 years
  • Subjects with previous history of pulmonary nodules.

Trial locations and contacts

2 sites in 2 countries. Contact the study team or a site near you to ask about taking part.

Luis Corrales, MD contact

+506 40202222

corrales@cimcacr.com

2 sites in 2 countries

Colombia1 site
  • CTIC

    Bogotá

    Andres Cardona, MD, Acardona@fctic.org

Other trials in Colombia

Costa Rica1 site
  • Centro de Investigacion y Manejo del Cancer (CIMCA)

    San José, Provincia de San José, 10103

    Luis Corrales, +506 40202222, corrales@cimcacr.com

Other trials in Costa Rica

About this study

Official title: A Prospective Observational Study to Determine the Utility of Lung Cancer Screening for Early Detection of Suspicious Lung Nodules in Latin America

Prospective study to assess lung cancer screening with low dose CT scan (LDCT) in Latin America (LATAM) and prospectively evaluate chest-XRay analyzed with artificial intelligence (AI) using qXRin (QURE ai) at the initial visit correlating with the findins of the initial LDCT in patients with other high risk criteria to develop lung cancer. 2000 patients will be recruited in 4 LATAM countries (Mexico 700 pts, Costa Rica 300 pts, Colombia 500 pts, Argentina 500 pts). All patients will be ≥50years of age with one of the following additional inclusion criteria: a. exposure to wood smoke (at least 100 hours/year), b.family history of lung cancer in a first degree relative, c. COPD and/or emphysema, d. smokers with a tobacco index of 10 y or more. The exclusion criteria include: a. lung cancer diagnosis or other type of cancer 5 years prior to screening, b. loss of 10% of baseline weight 6 months before inclusion, c. ineligible for LDCT, d. life expectancy ≤5 years, and e. previous history of pulmonary nodules.

The primary objective of the study is the utility of LDCT-based lung cancer screening in identifying suspicious lung nodules in smokers and non-smokers across LATAM, with secondary objectives including: 1- Utility of qXR-LNMS (lung nodule malignancy score) of chest XRay for lung cancer risk assessment to exclude low risk patients from LDCT screening, 2- Utility of LDCT-based lung cancer screening in subjects with various risk profiles in LATAM, 3- Prevalence of lung nodules in the study population, 4-Mortality rate in the subjects diagnosed with an anomaly in the LDCT (with or without LC diagnosis).

Being tested
Chest X-Ray, Low Dose CT scan
Keywords
lung cancer, screening, low dose CT scan, lung nodule
Medical subject headings
Lung Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Chest X-Ray, Low Dose CT scanDiagnostic test

    Visit 1: chest XRay analyzed by qXR (QURE ai) and LDCT1

    Visit 2: LDCT2 : (12/24 months as applicable ± 2 weeks)(interval of LDCT2 is determined by the findings of the Visit 1)

    1. Low risk by qXR and Lung RADS 1 or 2: repeat in 24 months
    2. Low risk by qXR and Lung RADS 3, high risk by qXR and Lung RADS 1, 2, 3: repeat in 12 months

    Telephonic follow-up visits (at 6 month interval post LDCT2 for 2 years)

    Any Lung RADS 0, 4A, 4B, 4X or S will be assed in a thoracic oncology multidisciplinary team

Study groups in NCT07524803
Study groupRoleWhat they receive
Healthy volunteers2000 patients in 4 LATAM countries, ≥50years of age with one of the following: a. exposure to wood smoke (at least 100 hours/year), b.family history of LC in a first degree relative, c. COPD and/or emphysema, d. smokers with a tobacco index of 10 y or more. Patients will have the following interventios and follow-up: A- Visit 1: chest XRay analyzed by qXR and a LDCT1 B- Visit 2: LDCT2 : (12/24 months as applicable ± 2 weeks)(interval of LDCT2 is determined by the findings of the Visit 1) 1. Low risk by qXR and Lung RADS 1 or 2: repeat in 24 months 2. Low risk by qXR and Lung RADS 3, high risk by qXR and Lung RADS 1, 2, 3: repeat in 12 months C- Telephonic follow-up visits (at 6 month interval post LDCT2 for 2 years) Any Lung RADS 0, 4A, 4B, 4X or S will be assed in a thoracic oncology multidisciplinary team
Receives: Diagnostic Test: Chest X-Ray, Low Dose CT scan

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Utility of LDCT-based lung cancer screening in identifying suspicious lung nodules in smokers and non-smokers across LATAM

    Measured: From enrollment until 5 years of follow-up

Secondary outcomes (4)
  1. Utility of qXR-LNMS of CXR for lung cancer risk assessment to exclude low risk patients from LDCT screening

    Measured: From enrollment until 5 years of follow-up

  2. Utility of LDCT-based LC screening in subjects with various risk profiles in LATAM

    Measured: From enrollment until 5 years of follow-up

  3. Prevalence of lung nodules in the study population

    Measured: From enrollment until 5 years of follow-up

  4. Mortality rate in subjects diagnosed with an anomaly in the LDCT (with or without LC diagnosis)

    Measured: From enrollment until 5 years of follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Apr 2026
  2. Study start1 May 2026 (estimated)
  3. Primary completion1 May 2030 (estimated)
  4. Study completion1 May 2032 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
2,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07524803
Sponsor's protocol ID
CLICAP-001
Acronym
LUCAS-LATAM
Status last verified
Apr 2026
First submitted
6 Apr 2026
Last updated
13 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Publications

  • Carrot-Zhang J, Soca-Chafre G, Patterson N, Thorner AR, Nag A, Watson J, Genovese G, Rodriguez J, Gelbard MK, Corrales-Rodriguez L, Mitsuishi Y, Ha G, Campbell JD, Oxnard GR, Arrieta O, Cardona AF, Gusev A, Meyerson M. Genetic Ancestry Contributes to Somatic Mutations in Lung Cancers from Admixed Latin American Populations. Cancer Discov. 2021 Mar;11(3):591-598. doi: 10.1158/2159-8290.CD-20-1165. Epub 2020 Dec 2.

    PubMed 33268447
  • Corrales L, Rosell R, Cardona AF, Martin C, Zatarain-Barron ZL, Arrieta O. Lung cancer in never smokers: The role of different risk factors other than tobacco smoking. Crit Rev Oncol Hematol. 2020 Apr;148:102895. doi: 10.1016/j.critrevonc.2020.102895. Epub 2020 Jan 31.

    PubMed 32062313
  • Arrieta O, Zatarain-Barron ZL, Cardona AF, Corrales L, Martin C, Cuello M. Uniting Latin America Through Research: How Regional Research Can Strengthen Local Policies, Networking, and Outcomes for Patients With Lung Cancer. Am Soc Clin Oncol Educ Book. 2022 Apr;42:1-7. doi: 10.1200/EDBK_349951.

    PubMed 35503985
  • Cardona AF, Sanchez N, Gutierrez-Babativa L, Rojas L, Zuluaga J, Martinez S, Viola L, Carvajal C, Bogoya J, Prieto-Pinto L, Samaca-Samaca D, Robles A, Kock J, Martin C, Corrales L, Raez LE, Cordeiro de Lima V, Samtani S, Arrieta O. Clinical and economic impact of the availability of innovative therapies for advanced lung cancer in men in Latin America: a population-based secondary data study. Lancet Reg Health Am. 2025 Jul 2;49:101172. doi: 10.1016/j.lana.2025.101172. eCollection 2025 Sep.

    PubMed 40688567
  • Lam S, Bai C, Baldwin DR, Chen Y, Connolly C, de Koning H, Heuvelmans MA, Hu P, Kazerooni EA, Lancaster HL, Langs G, McWilliams A, Osarogiagbon RU, Oudkerk M, Peters M, Robbins HA, Sahar L, Smith RA, Triphuridet N, Field J. Current and Future Perspectives on Computed Tomography Screening for Lung Cancer: A Roadmap From 2023 to 2027 From the International Association for the Study of Lung Cancer. J Thorac Oncol. 2024 Jan;19(1):36-51. doi: 10.1016/j.jtho.2023.07.019. Epub 2023 Jul 23.

    PubMed 37487906

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