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      Peptide vaccinations elicited strong immune responses that were reboosted by anti-PD1 therapy in a patient with myxofibrosarcoma.

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          Abstract

          Peptide-based immunotherapy does not usually elicit strong immunological and clinical responses in patients with end-stage cancer, including sarcoma. Here we report a myxofibrosarcoma patient who showed a strong clinical response to peptide vaccinations and whose immune responses were reboosted by anti-PD1 therapy combined with peptide vaccinations. The 46-year-old man showed a strong response to the peptide vaccinations (papillomavirus binding factor peptide, survivin-2B peptide, incomplete Freund's adjuvant, and polyethylene glycol-conjugated interferon-alpha 2a) and subsequent wide necrosis and massive infiltration of CD8+ T cells in a recurrent tumor. The patient's immune responses weakened after surgical resection; however, they were reboosted following the administration of nivolumab combined with peptide vaccinations. Thus, anti-PD1 therapy combined with peptide vaccinations might be beneficial, as suggested by the observations in this sarcoma patient.

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          Author and article information

          Journal
          Cancer Immunol Immunother
          Cancer immunology, immunotherapy : CII
          Springer Science and Business Media LLC
          1432-0851
          0340-7004
          Feb 2020
          : 69
          : 2
          Affiliations
          [1 ] Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060-8556, Japan. tukahara@sapmed.ac.jp.
          [2 ] Department of Pathology, Sapporo Medical University School of Medicine, South-1, West-17, Chuo-ku, Sapporo, 060-8556, Japan.
          [3 ] Department of Cancer Immunology, Medical and Biological, Laboratories Co., Ltd, 1063-103 Terasawaoka, Ina, 396-0002, Japan.
          [4 ] Department of Orthopaedic Surgery, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo, 060-8543, Japan.
          [5 ] Surgery Branch, Higashi-Sapporo Hospital, 7-35, 3-3 Higashi-Sapporo, Shiroishi-ku, Sapporo, 003-8585, Japan.
          [6 ] Odori Breast Thyroid Gland Clinic, 11, South-1, West-6, Chuo-ku, Sapporo, 060-0061, Japan.
          [7 ] Department of Surgery, Shin-Yamanote Hospital, 3-6-1 Suwa-cho, Higashimurayama, 189-0021, Japan.
          [8 ] Department of Surgery, Fuchinobe General Hospital, 3-2-8, Fuchinobe, Sagamihara, 252-0206, Japan.
          [9 ] Department of Pathology, Shin-Yamanote Hospital, 3-6-1 Suwa-cho, Higashimurayama, 189-0021, Japan.
          [10 ] Department of Diagnostic Pathology, Tokyo Medical University Hachioji Medical Center, 1163 Tate-machi, Hachioji, 193-0998, Japan.
          [11 ] Oncology Branch, Higashi-Sapporo Hospital, 7-35, 3-3 Higashi-Sapporo, Shiroishi-ku, Sapporo, 003-8585, Japan.
          [12 ] Department of Surgical Pathology, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo, 060-8543, Japan.
          Article
          10.1007/s00262-019-02455-0
          10.1007/s00262-019-02455-0
          31853575
          2eaf9767-291f-4a94-87c2-673173cb85a9
          History

          HLA-A24,Immune monitoring,Immunotherapy,PBF,Survivin
          HLA-A24, Immune monitoring, Immunotherapy, PBF, Survivin

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