This is a multicenter screening protocol designed to identify patients with NSCLC who have tumor mutations in the KEAP1 or NRF2/NFE2L2 genes in order to determine potential eligibility for a biomarker selected clinical trial (CX-839-014, otherwise known as the KEAPSAKE trial). Circulating tumor DNA (ctDNA) present in blood samples collected from eligible patients will be analyzed by next generation sequencing (NGS) for selected biomarkers. A commercial liquid biopsy NGS test will be provided to study participants free of charge.
Study Type
OBSERVATIONAL
Enrollment
20
Southern Cancer Center
Daphne, Alabama, United States
Southern Cancer Center - 3 Mobile Infirmary Circle
Mobile, Alabama, United States
Southern Cancer Center - Dauphin St
Mobile, Alabama, United States
Southern Cancer Center - Providence Hospital
Mobile, Alabama, United States
Arizona Oncology Associates - Glendale
Glendale, Arizona, United States
Positive KEAP1 or NRF2/NFE2L2 mutational status, assessed by NGS of blood ctDNA
The percentage of patients with nonsquamous NSCLC containing pathogenic NRF2/NFE2L2 and/or KEAP1 mutations
Time frame: Up to 16 months
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Arizona Oncology Associates - E. Highland Ave.
Phoenix, Arizona, United States
Arizona Oncology Associates - N. 27th Ave.
Phoenix, Arizona, United States
Arizona Oncology Associates
Scottsdale, Arizona, United States
Arizona Oncology Associates - Tempe
Tempe, Arizona, United States
Rocky Mountain Cancer Centers - Aurora
Aurora, Colorado, United States
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