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NCT05478538 | RECRUITING | Non Small Cell Lung Cancer

Observational Lung Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform
Sponsor:

the elephant

Brief Summary:

The primary objective of this study is to determine the ex-vivo prognostic accuracy of the Cybrid live tumor diagnostic platform using in-vivo RECIST 1.1 as the reference method.

Condition or disease

Non Small Cell Lung Cancer

Metastatic Non Small Cell Lung Cancer

NSCLC

Metastatic NSCLC - Non-Small Cell Lung Cancer

Intervention/treatment

Core Needle or Forceps Biopsy

Detailed Description:

Cancer is a leading cause of death and despite many new drugs, a major diagnostic challenge remains knowing which drug will work best for a patient. A new class of drugs called immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment. However, current diagnostic methods (e.g. PDL1, MSI and TMB) do not accurately predict which patients will respond. Elephas is developing a diagnostic platform using small 3D Live Tumor Fragments (LTFs) from participants for accurate prediction of drug response with a focus on ICIs such as Pembrolizumab (Keytruda). These LTFs contain both tumor cells and infiltrating immune cells, which are critical in determining response to ICIs and other immunotherapies. In this observational clinical trial, 200 Non-Small Cell Lung Cancer (NSCLC) participants will be recruited and their actual clinical response to ICIs (using RECIST 1.1) will be compared to the platform's predictive Artificial Intelligence (AI) score that is based on RNA, clinical data, and 3D microscopy images. The sensitivity and specificity of the platform's score will be determined and compared to current diagnostic methods for ICIs like PDL1, MSI, and TMB.

Study Type : OBSERVATIONAL
Estimated Enrollment : 200 participants
Official Title : Observational Lung Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform (CYBRID-01)
Actual Study Start Date : 2023-01-31
Estimated Primary Completion Date : 2026-12
Estimated Study Completion Date : 2026-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Subject Inclusion Criteria
  • 1. Written informed consent and HIPAA authorization for release of personal health information prior to registration. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.
  • 2. Age ≥ 18 years at the time of consent.
  • 3. Subjects suspected of or diagnosed with Stage IV/metastatic NSCLC and meet one of the following criteria
    • 1. Subjects who are undiagnosed, have undergone imaging and are suspected to have Stage IV lung cancer.
    • 2. Subjects with a previous Stage I, II, or III diagnosis of NSCLC, who are being re-biopsied due to suspected progression to metastatic disease.
    • 3. Subjects who have a newly confirmed diagnosis of Stage IV NSCLC, have undergone a SOC biopsy procedure and will undergo a separate procedure for the purposes of this study prior to starting first line treatment.
    • 4. Subjects who have a previous Stage IV/metastatic NSCLC diagnosis and have already received first line treatment.
    • 4. Subjects must be clinically able, at investigator discretion, to undergo additional CNB or forceps biopsy passes during their biopsy. These additional biopsies may either be collected from the primary tumor or a metastatic site amenable to additional passes (e.g., liver or lymph nodes) per the clinician.
    • 5. Subjects who are newly diagnosed or have suspected cancer must be treatment-naïve at the time of biopsy. All other subjects should have the biopsy performed before starting their next line of treatment.
    • Subject Exclusion Criteria
    • 1. Any patient for whom an extra biopsy might pose a clinical risk based on the discretion of the clinician.
    • 2. Any mental impairment that would render the patient unable to understand his/her participation in the study would disqualify the patient from consenting and participating.
    • 3. Subjects with an auto-immune disease that would render them ineligible for immune- oncology treatment.
    • 4. Immunocompromised subjects, and subjects known to be HIV positive and currently receiving antiretroviral therapy. NOTE: Patients known to be HIV positive, but without clinician evidence of an immunocompromised state, are eligible for this trial.
    • 5. Subjects who are enrolled or plan to be enrolled in a blinded oncology treatment trial are not eligible.
    • 6. Subjects who are pregnant are not eligible.
    • Observational Lung Trial to Collect Tissue to Train and Validate a Live Tumor Diagnostic Platform

    Location Details

    NCT05478538

    Please Choose a site

    How to Participate

    Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

    Locations

    NOT YET RECRUITING

    United States, California

    UCLA Medical Center

    Los Angeles, California, United States, 90095

    RECRUITING

    United States, Maryland

    James M Stockman Cancer Institute

    Frederick, Maryland, United States, 21702

    NOT YET RECRUITING

    United States, New York

    New York Cancer & Blood Specialists

    Shirley, New York, United States, 11967

    TERMINATED

    United States, North Carolina

    University of North Carolina at Chapel Hill

    Chapel Hill, North Carolina, United States, 27599

    TERMINATED

    United States, Ohio

    Gabrail Cancer Center

    Canton, Ohio, United States, 44718

    RECRUITING

    United States, Texas

    JPS Health Network

    Fort Worth, Texas, United States, 76104

    RECRUITING

    United States, Texas

    Baylor Scott & White Research Institute

    Temple, Texas, United States, 76508