Lung Cancer Screening for Lung Cancer

(CHAMP Trial)

Not yet recruiting at 2 trial locations
LS
Overseen ByLaura Seegmiller
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Jill Kolesar
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The U.S. Preventive Services Task Force recommends annual lung cancer screening (LCS) with low-dose CT for adults aged 50-80 with a ≥20 pack-year smoking history who currently smoke or quit within the past 15 years. Despite insurance coverage, only 17% of eligible Iowans were screened in 2024. Barriers include the complexity of screening and competing demands in primary care. To address these challenges, investigators propose a two-part intervention: a blood-based screening test to simplify LCS and a community pharmacist-led referral program integrated into routine pharmacy care.

Eligible patients will be identified at Greenwood Pharmacy in Waterloo, Iowa. Interested individuals will be consented by a pharmacist and engaged in shared decision-making about LCS. Participants may decline screening, complete the DELFI Diagnostics FirstLook lung cancer screening blood test, or pursue CT screening through their primary care physician. Those choosing the blood test will be referred to Cedar Valley Family Medicine. Patients with a positive result will complete a standard shared decision-making visit with their PCP and, if appropriate, undergo confirmatory CT imaging. Patients with a negative result will enter a screening cohort and be re-screened annually for an additional year.

Who Is on the Research Team?

JK

Jill Kolesar, PharmD, MS, FCCP

Principal Investigator

University of Iowa

Are You a Good Fit for This Trial?

Inclusion Criteria

I am between 50 and 77 years old.
Smoking pack-year history of ≥ 20 years
Current smoker or quit smoking 15 or less years ago
See 1 more

Exclusion Criteria

Self-report of lung cancer screening in the last 12 months
Psychiatric illness/social situations that would limit compliance with study requirements

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Consent and Decision-Making

Participants engage in shared decision-making with a pharmacist about lung cancer screening options

1-2 weeks
1 visit (in-person)

Initial Screening

Participants undergo either the DELFI blood test or a low-dose CT scan for lung cancer screening

6 months
1 visit (in-person) for blood test or CT scan

Follow-up

Participants with a positive blood test undergo confirmatory CT imaging; all participants are monitored for safety and effectiveness

12 months
Annual follow-up visits

Annual Re-screening

Participants with a negative blood test are re-screened annually for an additional year

12 months
1 visit (in-person) annually

What Are the Treatments Tested in This Trial?

Interventions

  • DELFI Diagnostics FirstLook Lung Cancer Screening Blood Test
  • Low-Dose CT Scan

How Is the Trial Designed?

3

Treatment groups

Experimental Treatment

Active Control

Group I: DELFI FirstLook Lung Cancer Screening Blood TestExperimental Treatment1 Intervention
Group II: Low-Dose CTActive Control1 Intervention
Group III: No lung cancer screeningActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Jill Kolesar

Lead Sponsor

Eli Lilly and Company

Industry Sponsor

Trials
2,708
Recruited
3,720,000+
Dr. Daniel Skovronsky profile image

Dr. Daniel Skovronsky

Eli Lilly and Company

Chief Medical Officer since 2018

MD from Harvard Medical School

David A. Ricks profile image

David A. Ricks

Eli Lilly and Company

Chief Executive Officer since 2017

BSc from Purdue University, MBA from Indiana University