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

Trial opened at the following institutions:

Medical University of South Carolina