PRIMARY OBJECTIVE:
I. To determine the on-target efficacy of binimetinib and palbociclib in patients with operable RAS-mutant lung adenocarcinoma, colorectal, or pancreatic cancer.
SECONDARY OBJECTIVES:
I. Correlative analysis of gene expression analysis. II. Define immune subsets within the pre and post-treatment tumor tissue.
OUTLINE:
Patients receive palbociclib orally (PO) once daily (QD) and binimetinib PO twice daily (BID) for 14 days in the absence of disease progression or unacceptable toxicity. Within 1 week after last dose of study medication, patients undergo surgery.
After completion of study treatment, patients are followed up at 30 days.
Source: View full study details on ClinicalTrials.gov
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