RECRUITINGOBSERVATIONAL
MYLUNG Consortium Part 3: Observational Study
Molecularly Informed Lung Cancer Treatment in a Community Cancer Network: A Longitudinal Prospective RWE Study (MYLUNG Consortium Part 3: Observational Study)
About This Trial
This longitudinal study looks to quantify the testing timeline, operational barriers, and outcomes of biomarker-guided therapy in a large, community-based, and largely unselected patient population with early stage and advanced stage, treatment-naive non-small cell lung cancer, whether squamous or non-squamous.
Who May Be Eligible (Plain English)
Who May Qualify:
- Adult subjects (18 years and older) with newly diagnosed early stage, locally advanced or metastatic non-small cell lung cancer
- Must be eligible for systemic therapy based on the treating provider's assessment. If systemic therapy was recommended and documented by the treating provider but the patient declined, they can still be eligible for the study. Patients can be enrolled prior to start of treatment.
- Subjects who developed locally advanced or metastatic disease after receiving adjuvant or neoadjuvant therapy are eligible if the adjuvant/neoadjuvant therapy was completed at least 12 months prior to the development of locally advanced or metastatic disease
- Subjects must be enrolled within 30 days of initiation of systemic therapy
- Signed willing to sign a consent form
Who Should NOT Join This Trial:
- Stage IA at the time of enrollment
- Subjects with small cell lung cancer
- Subjects with Unknown primary tumor origin
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Adult subjects (18 years and older) with newly diagnosed early stage, locally advanced or metastatic non-small cell lung cancer
* Must be eligible for systemic therapy based on the treating provider's assessment. If systemic therapy was recommended and documented by the treating provider but the patient declined, they can still be eligible for the study. Patients can be enrolled prior to start of treatment.
* Subjects who developed locally advanced or metastatic disease after receiving adjuvant or neoadjuvant therapy are eligible if the adjuvant/neoadjuvant therapy was completed at least 12 months prior to the development of locally advanced or metastatic disease
* Subjects must be enrolled within 30 days of initiation of systemic therapy
* Signed informed consent
Exclusion Criteria:
* Stage IA at the time of enrollment
* Subjects with small cell lung cancer
* Subjects with Unknown primary tumor origin
Locations (17)
Southern Cancer Center, PC
Daphne, Alabama, United States
Arizona Oncology Associates, PC - NAHOA
Prescott Valley, Arizona, United States
Rocky Mountain Cancer Center
Denver, Colorado, United States
Cancer Care Centers of Brevard, Inc.
Palm Bay, Florida, United States
Woodlands Medical Specialists, PA
Pensacola, Florida, United States
Affiliated Oncologists, LLC
Chicago Ridge, Illinois, United States
Illinois Cancer Specialists
Niles, Illinois, United States
Maryland Oncology Hematology, P.A.
Silver Spring, Maryland, United States
Minnesota Oncology Hematology, P.A.
Minneapolis, Minnesota, United States
New York Oncology Hematology, P.C.
Albany, New York, United States
Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, United States
Willamette Valley Cancer Institute and Research Center
Eugene, Oregon, United States
Oncology & Hematology Associates of Southwest Virginia, Inc., DBA Blue Ridge Cancer Care
Blacksburg, Virginia, United States
Virginia Cancer Specialists, PC
Fairfax, Virginia, United States
Virginia Oncology Associates
Newport News, Virginia, United States
Shenandoah Oncology, P.C.
Winchester, Virginia, United States
Northwest Cancer Specialists, P.C.
Vancouver, Washington, United States