Mixed 20-peptide cancer vaccine in combination with docetaxel and dexamethasone for castration-resistant prostate cancer: a randomized phase II trial.
Administration, Oral
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Cancer Vaccines
/ administration & dosage
Combined Modality Therapy
/ adverse effects
Dexamethasone
/ administration & dosage
Docetaxel
/ administration & dosage
Double-Blind Method
Drug Administration Schedule
Humans
Infusions, Intravenous
Injections, Subcutaneous
Kallikreins
/ blood
Male
Middle Aged
Progression-Free Survival
Prostate-Specific Antigen
/ blood
Prostatic Neoplasms, Castration-Resistant
/ blood
Response Evaluation Criteria in Solid Tumors
T-Lymphocytes, Cytotoxic
/ immunology
Vaccines, Subunit
/ administration & dosage
Docetaxel
Immunotherapy
Multiple-peptide vaccine
Phase II trial
Prostate cancer
Journal
Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
21
01
2019
accepted:
21
01
2020
pubmed:
7
2
2020
medline:
10
5
2020
entrez:
7
2
2020
Statut:
ppublish
Résumé
A novel cancer vaccine consisting of 20 mixed peptides (KRM-20) was designed to induce cytotoxic T lymphocytes (CTL) against twelve different tumor-associated antigens. The aim of this phase II trial was to examine whether KRM-20 in combination with docetaxel and dexamethasone enhances the antitumor effects in patients with castration-resistant prostate cancer (CRPC). In this double-blind, placebo-controlled, randomized phase II study, we enrolled chemotherapy-naïve patients with CRPC from ten medical centers in Japan. Eligible patients were randomly assigned 1:1 centrally to receive either KRM-20 combined with docetaxel and dexamethasone (n = 25) or placebo with docetaxel and dexamethasone (n = 26). The primary endpoint was the difference in prostate-specific antigen (PSA) decline between each treatment. The rates of > 50% PSA decline in the two arms were similar (56.5% versus 53.8%; P = 0.851). Human leukocyte antigen (HLA)-matched peptide-specific immunoglobulin G (P = 0.018) and CTL (P = 0.007) responses in the KRM-20 arm significantly increased after treatment. The addition of KRM-20 did not increase toxicity. There were no between-group differences in progression-free or overall survival (OS). The addition of KRM-20 was safe, and similar PSA decline and HLA-matched peptide-specific CTL and IgG responses increased in combination with docetaxel and dexamethasone in CRPC patients. Subgroup analysis suggested that this treatment is favorable for CRPC patients with ≥ 26% lymphocytes or PSA levels of < 11.2 ng/ml, but further clinical trials comparing OS are required.
Identifiants
pubmed: 32025848
doi: 10.1007/s00262-020-02498-8
pii: 10.1007/s00262-020-02498-8
pmc: PMC7183507
doi:
Substances chimiques
Cancer Vaccines
0
Vaccines, Subunit
0
Docetaxel
15H5577CQD
Dexamethasone
7S5I7G3JQL
KLK3 protein, human
EC 3.4.21.-
Kallikreins
EC 3.4.21.-
Prostate-Specific Antigen
EC 3.4.21.77
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
847-857Subventions
Organisme : Ministry of Health, Labour and Welfare
ID : ID 2014110358
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