Phase I/II Study of Multiple-Vaccine Therapy Using Epitope Peptide Restricted to HLA-A*0201 in Combination With Tegafur/Uracil/Folinate in Treating Patients With Refractory Colorectal Cancer
VEGF receptor 1 and 2 are essential targets to tumor angiogenesis, and we identified that
peptides derived from these receptors significantly induce the effective tumor specific CTL
response in vitro and vivo. According to these findings, in this trial, we evaluate the
safety, clinical and immunological response of those peptides. Patients will be vaccinated
twice a week for 8 weeks. On each vaccination day, VEGFR1 peptide (1mg) and VEGFR2 peptide
(1mg) mixed with Montanide ISA 51 will be administered by subcutaneous injection. The
patients will also receive oral chemotherapy (Tegafur/Uracil/Folinate) simultaneously.
Repeated cycles of the vaccine and the chemotherapy will be administered until patients
develop progressive disease or unacceptable toxicity, whichever occurs first. In the phase I
study, we evaluate the safety and tolerability of these peptide vaccine. In the following
phase II study, we evaluate the immunological and clinical response of this vaccine therapy.
Interventional
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
safety(Phase I:toxicities as assessed by NCI CTCAE version3) and efficacy(Phase II:Feasibility as evaluated by RECIST)
2 months
Yes
Masaru Shinozaki, MD/PhD
Principal Investigator
Head, Department of Surgery
Japan: Institutional Review Board
CRC-A02-I, II
NCT00677612
May 2008
March 2009
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