Phase I clinical trial of multiple-peptide vaccination for patients with advanced biliary tract cancer

被引:78
作者
Aruga, Atsushi [1 ,2 ]
Takeshita, Nobuhiro [1 ]
Kotera, Yoshihito [1 ]
Okuyama, Ryuji [1 ]
Matsushita, Norimasa [1 ]
Ohta, Takehiro [1 ]
Takeda, Kazuyoshi [3 ]
Yamamoto, Masakazu [1 ]
机构
[1] Tokyo Womens Med Univ, Dept Surg Gastroenterol, Shinjuku Ku, Tokyo 1628666, Japan
[2] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[3] Juntendo Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1138421, Japan
关键词
Cancer vaccine; Peptide vaccine; Immunotherapy; Biliary tract cancer; PROSTATE-CANCER; TESTIS ANTIGENS; SAFETY; MULTICENTER; GEMCITABINE; CISPLATIN; ANTI-PD-1; ANTIBODY;
D O I
10.1186/1479-5876-12-61
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: The prognosis of patients with advanced biliary tract cancer (BTC) is extremely poor and only a few standard treatments are available for this condition. We performed a phase I trial to investigate the safety, immune response and anti-tumor effect of vaccination with three peptides derived from cancer-testis antigens. Methods: This study was conducted as a phase I trial. Nine patients with advanced BTC who had unresectable tumors and were refractory to standard chemotherapy were enrolled. Three HLA-A*2402 restricted epitope peptides-cell division cycle associated 1 (CDCA1), cadherin 3 (CDH3) and kinesin family member 20A (KIF20A)-were administered subcutaneously, and the adverse events and immune response were assessed. The clinical effects observed were the tumor response, progression-free survival (PFS) and overall survival (OS). Results: The three-peptide vaccination was well-tolerated up to a dose of 3 mg per peptide (9 mg total). No grade 3 or 4 adverse events were observed after vaccination. Peptide-specific T cell immune responses were observed in all patients and stable disease was observed in 5 of 9 patients. The median PFS and OS were 3.4 and 9.7 months. The Grade 2 injection site reaction and continuous vaccination after PD judgment appeared to be prognostic of OS. Conclusions: Multiple-peptide vaccination was well tolerated and induced peptide-specific T-cell responses.
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页数:11
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