Understanding genetic variants in lung adenocarcinoma among Mexican patients
Official title: Prevalence of Pathogenic or Likely Pathogenic Germline Variants in Cancer Predisposition Genes Among Patients With Lung Adenocarcinoma
Run by Instituto Nacional de Cancerologia de Mexico · NCT06181812 · Data updated 2026-11-12
This study is trying to find out how common certain genetic changes are in Mexican patients under fifty with lung adenocarcinoma to better understand their condition.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 16 Years to 85 Years |
| Sex | All |
| Enrollment | 332 (estimated) |
| Sponsor | Instituto Nacional de Cancerologia de Mexico Academic / other |
| Locations | 1 site (Mexico City, Mexico City) |
| Status | Recruiting |
| Started | December 15, 2022 |
| Main results expected | December 15, 2026 |
| Study ends | December 15, 2027 |
| Registry record updated | April 8, 2026 |
| Trial ID | NCT06181812 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include Mexican patients aged 16 and older with histologically confirmed lung adenocarcinoma.
✕Probably not a fit
Patients without accessible blood samples or insufficient clinical information may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to assess the prevalence of germline pathogenic variants in Mexican patients diagnosed with lung adenocarcinoma, particularly focusing on those under fifty years of age. It will explore the clinical-pathological characteristics associated with these variants and investigate the relationship between actionable somatic mutations and germline variants. Participants will provide a blood sample for DNA extraction and next-generation sequencing to identify genetic alterations. The study is designed to gather comprehensive data that could enhance understanding of lung adenocarcinoma genetics in this population.
Why it matters
Potential benefit: If successful, this study could lead to improved genetic screening and targeted therapies for lung adenocarcinoma patients.
How similar studies have gone: Other studies have shown success in identifying genetic variants in lung cancer, suggesting that this approach could yield valuable insights.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both sexes * ≥ 16 years old, according the institutional protocols for new patients admittances. * histologically confirmed lung adenocarcinoma (LUAD) * Signed written informed consent form * A life expectancy greater than 8 weeks. * Histologically confirmed LUAD and one of the following conditions: i) LCFH, defined as having one first-degree relative (FDR) or two or more second-degree relatives with LC, irrespective of the age at diagnosis. ii) Age at diagnosis ≤50 years, or ≤60 with a pack-years index. iii) Presence of ≥1 AGAs (EGFR, ALK, ROS1, KRAS, BRAF, MET exon 14 skipping, or RET). Exclusion Criteria: * A sample of peripheral blood that is not accessible. * Insufficient clinical pathological information in the electronic clinical record. Elimination Criteria: * Withdrawal * Insufficient DNA quality and quantity for genomic sequencing analyses. * Lost of follow up
Where it's running
-
Thoracic Oncology Unit and Personalized Medicine Laboratory, Instituto Nacional de Cancerología
Mexico City, Mexico City, Mexico Recruiting
Study contacts
- Principal investigator: Oscar G Arrieta Rodriguez, M.D., M.Sc. — Instituto Nacional de Cancerologia de Mexico
- Study coordinator: Oscar G Arrieta Rodriguez, M.D., M.Sc.
- Email: ogar@unam.mx
- Phone: 5556280400
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.