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Analysis of Screen-detected Lung Cancers' Genomic Traits (ASCENT)

University College London (UCL) logo

University College London (UCL)

Status

Enrolling

Conditions

Lung Cancer

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Prospective, observational cohort study of patients undergoing surgical resection for low dose CT (LDCT) screen-detected lung cancer (detected through the SUMMIT study- ClinicalTrials.gov Identifier: NCT03934866/ lung screening programmes), in which translational research is a fundamental aspect.

Full description

The ASCENT study seeks to examine the genomic signatures of screen-detected cancers, in order to categorise the biological behaviour of such lesions and correlate this against non-invasive biological and radiological parameters. From these data, the plan is to explore strategies to characterise LDCT-detected cancers through non-invasive means, which the researchers believe may prove key in mitigating potential screening-associated harms.

Enrollment

526 estimated patients

Sex

All

Ages

50 to 77 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosed with confirmed lung cancer or probable lung cancer via LDCT screening.
  2. Planned for, or completed primary surgical resection either for histologically confirmed lung cancer, or strongly suspected lung cancer.
  3. Able to provide written informed consent (or verbal informed consent for participants consenting to retrospective diagnostic samples and data collection only).

Exclusion criteria

  1. Treatment with neoadjuvant therapy for current lung malignancy as per local MDT treatment decision.
  2. Known Active Human Immunodeficiency Virus (HIV), Hepatitis B virus, Hepatitis C Virus or Syphilis.

Trial contacts and locations

2

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Central trial contact

Laura Hughes

Data sourced from clinicaltrials.gov

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