Unspecified Adult Solid Tumor, Protocol Specific Clinical Trial
Official title:
A Phase 1 Study of AZD6244 in Combination With Cetuximab in Refractory Solid Tumors
This phase I trial is studying the side effects and the best dose of MEK Inhibitor AZD6244 when given together with cetuximab in patients with advanced or refractory solid tumors that cannot be removed by surgery. MEK inhibitor AZD6244 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving MEK Inhibitor AZD6244 together with cetuximab may kill more tumor cells.
PRIMARY OBJECTIVES:
I. To determine the dose limiting toxicities and the maximum tolerated dose of AZD6244 in
combination with cetuximab in advanced, refractory solid tumors.
II. To assess for evidence of anti-tumor activity with this combination, per tumor
measurements using RECIST criteria.
SECONDARY OBJECTIVES:
I. To evaluate the pharmacokinetics of AZD6244 and cetuximab when administered
concomitantly.
II. To evaluate the safety and tolerability of the combination of AZD6244 and cetuximab in
patients with K-RAS mutated metastatic colorectal cancer.
TERTIARY OBJECTIVES:
I. To assess the inhibition of the RAF/MEK/ERK pathway in peripheral blood mononuclear cells
secondary to treatment with AZD6244.
II. To evaluate the pharmacokinetics of AZD6244 in combination with cetuximab and the
relation to treatment side effects.
OUTLINE: This is a dose-escalation study of MEK inhibitor AZD6244.
Patients receive oral MEK inhibitor AZD6244 once or twice daily on days 1-28 and cetuximab
IV over 60 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of
disease progression or unacceptable toxicity.
Blood samples are collected at baseline and periodically during study for pharmacokinetic
and biomarker analyses.
After completion of study treatment, patients are followed up for 1 month or every 3 months
for 1 year.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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