Immunological evaluation of personalized peptide vaccination for patients with histologically unfavorable carcinoma of unknown primary site
被引:0
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作者:
Shinjiro Sakamoto
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机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Shinjiro Sakamoto
Shigeru Yutani
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h-index: 0
机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Shigeru Yutani
Shigeki Shichijo
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h-index: 0
机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Shigeki Shichijo
Michi Morita
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h-index: 0
机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Michi Morita
Akira Yamada
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机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Akira Yamada
Kyogo Itoh
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机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Kyogo Itoh
Masanori Noguchi
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机构:Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
Masanori Noguchi
机构:
[1] Kurume University School of Medicine,Cancer Vaccine Center, Research Center for Innovative Cancer Therapy
[2] Kurume University School of Medicine,Clinical Research Division, Research Center for Innovative Cancer Therapy
[3] Hiroshima University School of Medicine,Department of Molecular and Internal Medicine
[4] Nagasaki University Graduate Biomedical Science,Department of Surgery
[5] Kurume University School of Medicine,Cancer Vaccine Division, Research Center for Innovative Cancer Therapy
来源:
Cancer Immunology, Immunotherapy
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2016年
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65卷
关键词:
Cancer immunotherapy;
Carcinoma of unknown primary site;
Metastasis;
Personalized peptide vaccine;
Unfavorable subsets;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
The immunological characteristics of carcinoma of unknown primary site (CUP) are not well established due to inclusion of heterogeneous types of metastatic tumors with the absence of any detectable primary site. We evaluated the immune responses in patients with histologically unfavorable CUP during personalized peptide vaccination (PPV). Ten patients with histologically unfavorable CUP who had been treated by PPV after chemotherapy failure were analyzed. In PPV treatment, up to four human leukocyte antigen-matched peptides of a total 31 peptides were selected according to preexisting host immunity before vaccination and administered subcutaneously. Peptides derived from the Lck antigen were most often chosen for use among all patients. CTL responses were increased in 8 of the 10 and 5 of the five patients tested at the end of the first and second PPV cycles, respectively. Increases in humoral responses after vaccination, including IgG, IgG1, IgG3, IgA, and IgM, were observed against not only the vaccinated peptides but also the non-vaccinated peptides. Severe adverse events due to PPV were not observed. Median overall survival was 13.9 months (95 % CI 4.0–22.5 months). PPV activated both cellular and humoral immune responses to short peptides derived from CTL epitopes in the majority of CUP patients. PPV with Lck-derived peptides may be a feasible, new treatment modality for histologically unfavorable CUP patients due to its safety and strong ability to boost immune responses, although its clinical efficacy remains to be investigated in larger-scale trials.