GEMINI-NSCLC: NSCLC Biomarker Study
Sponsored by Tempus AI
About this study
GEMINI NSCLC Study is a non-interventional study that will be collecting clinical and molecular health information from patients with NSCLC who will receive longitudinal blood collection in addition to their standard of care therapy and disease surveillance with the goals of identifying the molecular evolution of lung cancer with standard of care therapy, and determining the utility of ctDNA dynamics to predict risk of recurrence and therapeutic outcomes.
Where this study is enrolling (56)
- I'm interested
Alabama Oncology
Birmingham, Alabama
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Mercy Clinic Oncology - Fort Smith
Fort Smith, Arkansas
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MemorialCare
Fountain Valley, California
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UCLA
Los Angeles, California
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Eastern CT and Hematology and Oncology Associates
Norwich, Connecticut
Show all 56 locations
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Clermont Oncology Center
Clermont, Florida
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Piedmont Healthcare
Atlanta, Georgia
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Morehouse School of Medicine (MSM)
Atlanta, Georgia
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Hawaii Cancer Care
Honolulu, Hawaii
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Cancer Care Specialists of Illinois
Decatur, Illinois
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Southern Illinois Hospital Services
Carterville, Illinois
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OSF Saint Anthony Medical Center
Rockford, Illinois
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Northwestern University
Evanston, Illinois
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Hope and Healing Cancer Services
Hinsdale, Illinois
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Community Health Network
Indianapolis, Indiana
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University of Iowa
Iowa City, Iowa
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University of Maryland
Baltimore, Maryland
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Johns Hopkins University
Baltimore, Maryland
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Frederick Health Regional System
Frederick, Maryland
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The Center for Cancer and Blood Disorder
Bethesda, Maryland
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Lake Regional Health System
Osage Beach, Missouri
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Mercy Clinic Cancer and Hematology - Chub O'Reilly Cancer Center
Springfield, Missouri
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Mercy Clinic Oncology and Hematology - David C. Pratt Cancer Center
St Louis, Missouri
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Mercy Clinic Oncology and Hematology - Joplin
Joplin, Missouri
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Mercy Clinic Oncology and Hematology - Sindelar Cancer Center
St Louis, Missouri
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Oncology Hematology Associates
Springfield, Missouri
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Nebraska Cancer Specialists
Omaha, Nebraska
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Hope Cancer Care of Nevada
Las Vegas, Nevada
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Cancer Care Specialists Reno
Reno, Nevada
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OptumCare Cancer Care
Las Vegas, Nevada
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New Jersey Cancer Center
Belleville, New Jersey
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White Plains Hospital
White Plains, New York
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Icahn School of Medicine at Mount Sinai
New York, New York
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New York Oncology Hematology
Albany, New York
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Hematology Oncology Associates of Central New York
East Syracuse, New York
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Cayuga Medical Center
Ithaca, New York
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Duke University
Durham, North Carolina
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Southeastern Medical Oncology Center (SMOC)
Goldsboro, North Carolina
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UNC
Chapel Hill, North Carolina
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Taylor Cancer Research Center
Maumee, Ohio
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Ohio State University
Columbus, Ohio
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Aultman Hospital
Canton, Ohio
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TriHealth Cancer Institute
Cincinnati, Ohio
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OhioHealth Reseach Institute
Columbus, Ohio
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Mercy Clinic Oncology and Hematology - Coletta
Oklahoma City, Oklahoma
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Oklahoma Cancer Specialists and Research Institute
Tulsa, Oklahoma
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Hightower Clinical
Oklahoma City, Oklahoma
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Oregon Oncology Specialists
Salem, Oregon
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Cancer Care Associates of York
York, Pennsylvania
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The Medical University of South Carolina
Charleston, South Carolina
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Baptist Cancer Center
Memphis, Tennessee
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University of Virginia
Charlottesville, Virginia
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PeaceHealth St. Joseph Medical Center-Bellingham
Bellingham, Washington
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Cancer Care Northwest
Spokane Valley, Washington
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ThedaCare Regional Cancer Center
Appleton, Wisconsin
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Gundersen Health System
La Crosse, Wisconsin
Who can participate
Exclusion criteria
- ✕Tumors that lack activating EGFR mutations (e.g., exon 19 deletion or exon 21 L858R, exon 21 L861Q, exon 18 G719X, or exon 20 S768I mutation) and ALK fusions. Also, per NCCN Guideline recommended testing, tumors must also lack ROS1, BRAF, NTRK 1/2/3, METex14 skipping mutations, and RET for which there is available front-line targeted therapy. Only those patients with KRAS G12C mutations and ERBB2 (HER2) mutations with no contraindications to immunotherapy (PD-L1 1) for which there are no approved front-line targeted therapies and for whom immunotherapy would be the preferred front-line therapy are eligible.
- ✕Patients may be enrolled with local molecular testing and those results will be provided.
- ✕Patients may be enrolled with local molecular testing and those results will be provided.
- ✕18 years and older
- ✕Willing and able to provide informed consent
- ✕Willing to have additional blood samples collected during routine surveillance visits
- ✕Must submit tumor sample representative of current disease
- ✕Exclusion Criteria (both Cohorts):
- ✕Patients without a known or suspected NSCLC diagnosis, or other disease processes such as sarcoidosis, lymphoma, or metastatic cancer from other sites.
- ✕Not willing to have additional blood samples collected
- ✕Patients with a secondary malignancy must have been both diagnosed \> 2 years from the lung cancer of interest and have completed all therapy for that malignancy (including extended adjuvant therapy) \> 2 years prior to diagnosis of the lung cancer of interest with the exception of the following:
- ✕Patients with superficial basal cell carcinoma of low-risk histology per NCCN Guidelines (Low-risk histologic subtypes include nodular, superficial, and other non-aggressive growth patterns such as keratotic, infundibulocystic, and fibroepithelioma of Pinkus) and low-risk for recurrence per NCCN Guidelines (location on trunk or extremities, size \< 2 cm, primary (not recurrent), with well-defined borders) can be included even if they are diagnosed \< 2 years from the lung cancer of interest.
- ✕Patients with superficial squamous cell carcinoma of low-risk pathology per NCCN Guidelines (verrucous, keratoacanthomatous) and low-risk for recurrence per NCCN Guidelines (located on trunk or extremities; 2 cm in size; primary lesion (vs. recurrent); well to moderately differentiated; \< 2 mm thick and no invasion beyond subcutaneous fat; negative for perineural invasion; and negative for lymphatic or vascular involvement) can be included even if they are diagnosed \< 2 years from the lung cancer of interest.
Only the research team can confirm whether you qualify. The intake questionnaire is the best way to find out.
Completing a questionnaire on Clinably does not enroll you in a clinical trial or confirm your eligibility. Only the research team can determine whether you qualify to participate. These results are based on the information you provide and are intended to help you start a conversation with the research team.
Trial data sourced from ClinicalTrials.gov.