The purpose of this study is to evaluate overall survival and immunological monitoring for peptide vaccination therapy using novel cancer testis antigens for locally advanced, recurrent, or metastatic esophageal squamous cell carcinoma (ESCC).
The phase I vaccination study using peptides derived from TTK, LY6K, and IMP-3 for locally advanced, recurrent or metastatic esophageal squamous cell carcinoma (ESCC) who had failed for the standard therapy indicated that the vaccine treatment were well tolerated and feasible, and that antigen-specific T cell responses were strongly induced by the vaccination with some objective clinical responses. Thus, we are currently initiating the randomized phase II clinical vaccination study for the same cohort with ESCC to evaluate the survival benefit of the cancer vaccination.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Each of three peptides (1mg) mixed with IFA (1ml) were injected every week at five round.
First Department of Surgery, University of Yamanashi
Chūō, Yamanashi, Japan
RECRUITINGOverall survival after the 1st vaccination
Time frame: 2 years
Antigen specific control response induced by vaccination
Time frame: 1 year
DTH response induced by vaccination
Time frame: 1 year
Time to progression after the 1st vaccination
Time frame: 1 year
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