Neoadjuvant Screening Trial: LCMC4 Evaluation of Actionable Drivers in Early Stage Lung Cancer
- Sponsor:
- Lung Cancer Mutation Consortium
- Sponsor Study ID:
- LCMC4
- CTO #:
- 103745
- NCT Number:
- NCT04712877
- Phase:
- N/A
- Protocol Type:
- Screening
- Age Group:
- Adults
- Disease Sites:
- Lung
- Study Objectives:
- The primary objective of this study is to determine the proportion of patients with stage IA2-III lung cancers who possess actionable oncogenic drivers. The screening approach will be considered feasible if, utilizing tumor or plasma assays, 35% of non-squamous non-small cell lung cancers are identified as having a actionable genomic alteration including ALK rearrangements, BRAFV600E mutations, EGFR sensitizing mutations, HER2 mutation, HER2 amplification, MET amplification, MET exon 14 mutation, RET rearrangements, NTRK rearrangement, KRAS G12C, or ROS1 rearrangements
- eConsent:
- Not available
- Study Documents:
-
Open Study Documents
(MUSC NetID required for document access)
For more information about this trial please contact the study team:
-
Medical University of South Carolina
- Principal Investigator, Engelhardt, Kathryn, at engelhar@musc.edu , or please call +1 330-671-3455.
- Study Coordinator, Shealor, Jessica, at shealorj@musc.edu .
Trial opened at the following institutions:
Medical University of South Carolina