Literature DB >> 26728480

A randomized phase II clinical trial of personalized peptide vaccination with metronomic low-dose cyclophosphamide in patients with metastatic castration-resistant prostate cancer.

Masanori Noguchi1,2,3, Fukuko Moriya4, Noriko Koga5, Satoko Matsueda6, Tetsuro Sasada7, Akira Yamada8, Tatsuyuki Kakuma9, Kyogo Itoh6.   

Abstract

This study investigated the effect of metronomic cyclophosphamide (CPA) in combination with personalized peptide vaccination (PPV) on regulatory T cells (Treg) and myeloid-derived suppressor cells (MDSC), and whether it could improve the antitumor effect of PPV. Seventy patients with metastatic castration-resistant prostate cancer were randomly assigned (1:1) to receive PPV plus oral low-dose CPA (50 mg/day), or PPV alone. PPV treatment used a maximum of four peptides chosen from 31 pooled peptides according to human leukocyte antigen types and antigen-specific humoral immune responses before PPV, for 8 subcutaneous weekly injections. Peptide-specific cytotoxic T lymphocyte (CTL) and immunoglobulin G responses were measured before and after PPV. The incidence of grade 3 or 4 hematologic adverse events was higher in the PPV plus CPA arm than in the PPV alone arm. Decrease in Treg and increase in MDSC were more pronounced in PPV plus CPA treatment than in PPV alone (p = 0.036 and p = 0.048, respectively). There was no correlation between the changes in Treg or MDSC and CTL response. There was no difference in positive immune responses between the two arms, although overall survival in patients with positive immune responses was longer than in those with negative immune responses (p = 0.001). Significant differences in neither progression-free survival nor overall survival were observed between the two arms. Low-dose CPA showed no change in the antitumor effect of PPV, possibly due to the simultaneous decrease in Treg and increase in MDSC, in patients under PPV.

Entities:  

Keywords:  Cyclophosphamide; Immunotherapy; Myeloid-derived suppressor cell; Peptide vaccination; Phase II trial; Regulatory T cell

Mesh:

Substances:

Year:  2016        PMID: 26728480     DOI: 10.1007/s00262-015-1781-6

Source DB:  PubMed          Journal:  Cancer Immunol Immunother        ISSN: 0340-7004            Impact factor:   6.968


  28 in total

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Review 4.  Classes of therapeutics to amplify the immune response.

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Journal:  Breast Cancer Res Treat       Date:  2021-11-17       Impact factor: 4.624

5.  mRNA-transfected dendritic cell vaccine in combination with metronomic cyclophosphamide as treatment for patients with advanced malignant melanoma.

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Journal:  Oncoimmunology       Date:  2016-07-08       Impact factor: 8.110

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Authors:  Takahiro Kimura; Shin Egawa; Hirotsugu Uemura
Journal:  Nat Rev Urol       Date:  2017-05-31       Impact factor: 14.432

Review 7.  Harnessing the immune system to improve cancer therapy.

Authors:  Nikos E Papaioannou; Ourania V Beniata; Panagiotis Vitsos; Ourania Tsitsilonis; Pinelopi Samara
Journal:  Ann Transl Med       Date:  2016-07

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Authors:  Adriana Romiti; Rosa Falcone; Michela Roberto; Paolo Marchetti
Journal:  Invest New Drugs       Date:  2016-12-01       Impact factor: 3.651

9.  Phase II clinical trial of peptide cocktail therapy for patients with advanced pancreatic cancer: VENUS-PC study.

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Journal:  Cancer Sci       Date:  2016-12-19       Impact factor: 6.716

10.  Prediction of the efficacy of immunotherapy by measuring the integrity of cell-free DNA in plasma in colorectal cancer.

Authors:  Masahiro Kitahara; Shoichi Hazama; Ryouichi Tsunedomi; Hiroko Takenouchi; Shinsuke Kanekiyo; Yuka Inoue; Masao Nakajima; Shinobu Tomochika; Yoshihiro Tokuhisa; Michihisa Iida; Kazuhiko Sakamoto; Nobuaki Suzuki; Shigeru Takeda; Tomio Ueno; Shigeru Yamamoto; Shigefumi Yoshino; Hiroaki Nagano
Journal:  Cancer Sci       Date:  2016-12-18       Impact factor: 6.716

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