| Literature DB >> 27072896 |
Mutsunori Murahashi1, Yasuki Hijikata1, Kazunari Yamada1, Yoshihiro Tanaka2, Junji Kishimoto3, Hiroyuki Inoue2, Tomotoshi Marumoto2, Atsushi Takahashi2, Toshihiko Okazaki1, Kazuyoshi Takeda4, Masakazu Hirakawa5, Hiroshi Fujii6, Shinji Okano6, Masaru Morita7, Eishi Baba8, Kazuhiro Mizumoto9, Yoshihiko Maehara7, Masao Tanaka9, Koichi Akashi8, Yoichi Nakanishi10, Koji Yoshida11, Takuya Tsunoda11, Kazuo Tamura12, Yusuke Nakamura11, Kenzaburo Tani13.
Abstract
We designed a phase I trial to investigate the safety, immune responses and clinical benefits of a five-peptide cancer vaccine in combination with chemotherapy. Study subjects were patients positive for HLA-A2402 with locally advanced, metastatic, and/or recurrent gastrointestinal, lung or cervical cancer. Eighteen patients including nine cases of colorectal cancer were treated with escalating doses of cyclophosphamide 4days before vaccination. Five HLA-A2402-restricted, tumor-associated antigen (TAA) epitope peptides from KOC1, TTK, URLC10, DEPDC1 and MPHOSPH1 were injected weekly for 4weeks. Treatment was well tolerated without any adverse events above grade 3. Analysis of peripheral blood lymphocytes showed that the number of regulatory T cells dropped from baseline after administration of cyclophosphamide and confirmed that TAA-specific T cell responses were associated significantly with longer overall survival. This phase I clinical trial demonstrated safety and promising immune responses that correlated with vaccine-induced T-cell responses. Therefore, this approach warrants further clinical studies.Entities:
Keywords: Cyclophosphamide; Five-peptide cancer vaccine; Regulatory T cells; Translational research
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Year: 2016 PMID: 27072896 DOI: 10.1016/j.clim.2016.03.015
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969