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NCT06934343Recruiting

Machine Learning Approaches to Personalized Therapy for Advanced Non-small Cell Lung Cancer With Real-World Data

Source: ClinicalTrials.gov · Last updated 4 May 2026

Brief summary (registry, in English)

This research will leverage machine learning (ML) and causal inference techniques applied to real-world data (RWD) to generate evidence that personalizes treatment strategies for patients with advanced non-small cell lung cancer (aNSCLC). Rather than influencing regulatory decisions or clinical guidelines, the goal of this trial is to refine treatment selection among existing therapeutic options, ensuring that care is tailored to individual patient characteristics. Additionally, by generating real-world evidence, these findings will inform the design and implementation of future clinical trials. Importantly, the methodological advancements will establish a pipeline that extends beyond aNSCLC, facilitating the identification of optimal dynamic treatment regimes (DTRs) for other complex diseases.

Status (registry)
Recruiting
Study type
Observational
Enrollment
144400 (estimated)
First submitted
28 Feb 2025
Start date
1 Sept 2024
Primary completion date
31 Aug 2027
Lead sponsor
University of Utah
NCT number
NCT06934343

What you commit to

  • Study type: Observational
  • Planned participants: 144400
  • From 1 Sept 2024 to the primary completion date, 31 Aug 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Fewer than one day of follow-up post-initiation of first-line (1L) therapy.
  • First-line treatment limited to immunotherapy or chemoimmunotherapy (excluding other treatment regimens).
  • Patients receiving second-line (2L) treatment, including those enrolled in a clinical study.

Lab values

  • Presence of a targetable mutation, including ALK, BRAF, EGFR, KRAS, or ROS1.

Other

  • Subjects meeting any of the following criteria at baseline will be excluded:
  • PD-L1 expression \<50% at baseline (restricted to patients with PD-L1 ≥50%).

Who the study is looking for

  • Subjects must meet all of the following eligibility criteria:
  • Diagnosed with advanced NSCLC between January 1, 2011, and June 30, 2024.
  • Follow-up available until December 31, 2024, with a minimum potential follow-up period of at least six months.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Huntsman Cancer Institute at the University of Utah
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.