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NCT Number: NCT06716580

EQUAL: EGFR ctDNA QUantative Assessment for Lung Cancer Screening in Asian and Latinx Populations

This research study is studying a new blood test to screen for Epidermal Growth Factor Receptor (EGFR) positive lung cancer in healthy individuals at risk for the disease and who cannot undergo regular lung cancer screening.

The name of the test used in this research study is:

-Circulating free DNA (cfDNA) Assay

Recruiting

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

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About this study

The goal of this research study is to evaluate the feasibility of a novel EGFR blood plasma ctDNA screening test among East Asian and Latinx participants at risk for lung cancer and ineligible for regular lung cancer screening. The test looks for a gene change called Epidermal Growth Factor Receptor (EGFR), specifically EGFR L858R and exon 19 deletions, which comprise 85-90% of total EGFR mutations. This study seeks to determine if it is possible to use the blood test to detect this type of lung cancer that might not yet show symptoms.

The research study procedures include screening for eligibility, in-clinic visits, blood tests, and an optional questionnaire and/or focus group.

It is expected that about 1000 people will participate in the blood sample collection, 100 individuals in the survey, and 20 individuals in the focus groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(Aims 1, 2, and 3) for Group 1 (50 through 80 years of age):

  • Non-tobacco using (currently)
  • Self-identify as East Asian (including Southeast Asian) or Hispanic/Latinx.
  • East Asian includes those who self-identify as Chinese, Japanese, Korean, Taiwanese, Malaysian
  • Southeast Asian includes those who self-identify as Cambodian, Thai, Vietnamese, Filipino
  • Latinx includes those who self-identify as a person of Central or South American and the Caribbean including, Cuban, Puerto Rican, and Dominican culture or origin, excluding individuals originating from Spain
  • Aims 1 and 2: Able to complete and understand the study's informed consent in English, Mandarin, Cantonese, Japanese, Korean, Vietnamese, Spanish, Portuguese, or Cape Verdean
  • Aim 3: Able to complete and understand the study's informed consent and participate in a focus group in English, Mandarin, Vietnamese, or Spanish.

Inclusion criteria

(Aims 1, 2, and 3) for Group 2 (40 through 49 years of age):

  • Non-tobacco using (currently)
  • Self-identify as East Asian (including Southeast Asian) or Latinx, if any of the following criteria are met:
  • Family history of EGFR positive LC L858R or exon 19
  • Personal history of remote cancer that is not LC or other thoracic malignancies, including thymoma, thymic carcinoma, or sarcoma, as long as it was resolved over 5 years ago
  • History of TB, asthma requiring daily inhaled corticosteroids or chronic bronchitis
  • Symptoms of lung cancer for the past month, including hemoptysis, unexplained weight loss, voice hoarseness, cough or worsening cough, dyspnea or worsening dyspnea
  • Excluding individuals who concurrently present with fever, covid/influenza/RSV/adenovirus infection, runny nose, sore throat, productive cough with green or yellow sputum
  • Aims 1 and 2: Able to complete and understand the study's informed consent in English, Mandarin, Cantonese, Japanese, Korean, Vietnamese, Spanish, Portuguese, or Cape Verdean
  • Aim 3: Able to complete and understand the study's informed consent and participate in a focus group in English, Mandarin, Vietnamese, or Spanish.

Exclusion criteria

(Aims 1, 2, and 3) for Groups 1 and 2:

  • Having had a chest CT scan in the last 3 years or having an anticipated chest CT scan during the enrollment period.
  • Having a current cancer or history of cancer within the last 5 years, excluding localized non-melanoma skin cancer and breast ductal carcinoma in situ.
  • More than 400 lifetime cigarettes (i.e., 20 packs) of smoking or tobacco use
  • Adults unable to provide informed consent
  • Individuals <40 years of age
  • Prisoners
  • Pregnant women
  • Personal diagnosis of lung cancer
  • Not able to be compliant with study requirements

Treatment and study plan

Circulating Tumor DNA (ctDNA) Assay

Device

Screening investigational blood test to test for EGFR L858R and exon 19 deletions, which comprise 85-90% of total EGFR mutations. A positive or indeterminate investigational test will be followed up by CLIA verification of results. A positive or indeterminate CLIA result will be followed up by a lung CT scan. A positive CT scan will be followed up by referral for further evaluation. A negative CT scan will be followed up by a repeat scan in 12 months.

Primary outcomes

  1. Detection Rate of Non-Small Cell Lung Cancer

    Time frame: 2 years

    The proportion of participants with a positive assay result who are subsequently diagnosed with lung cancer through clinical pathology, among all participants tested with the assay.

Secondary outcomes

  1. Testing Turnaround Time

    Time frame: Up to 2 years

    The duration from the time of blood draw to the release of the ctDNA testing results to the study team.

  2. Recruitment Acceptability

    Time frame: Up to 2 years

    Determining proportion of screened patients who are eligible and who consent to the trial at each collaboration site

  3. Barriers to Sample Acquisition

    Time frame: Up to 2 years

    Examining barriers impeding scale-up of sample collection, handling, and delivery

Study contacts

Contact information is provided by the study sponsor or research team.

Fernando Pacheco

CONTACT

[email protected]

857-215-2794

Kylee Coonradt

CONTACT

[email protected]

617-582-8846

Sponsors and collaborators

Lead sponsor

Dana-Farber Cancer Institute

Other

Collaborators

  • Beth Israel Deaconess Medical Center
  • Boston Medical Center
  • Massachusetts General Hospital

Registry information

Acronym: EQUAL

Important dates

Study start
2025
Primary completion
2027
Study completion
2030
First posted
Dec 4, 2024
Registry last updated
Jul 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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