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首页> 外文期刊>Cancer immunology, immunotherapy : >Mixed 20-peptide cancer vaccine in combination with docetaxel and dexamethasone for castration-resistant prostate cancer: a randomized phase II trial
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Mixed 20-peptide cancer vaccine in combination with docetaxel and dexamethasone for castration-resistant prostate cancer: a randomized phase II trial

机译:混合20-肽癌疫苗与多西紫杉醇和地塞米松组合用于抗阉割的前列腺癌:随机期II试验

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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-naive 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.
机译:设计了一种由20种混合肽(KRM-20)组成的新型癌症疫苗,以诱导针对12种不同肿瘤相关抗原的细胞毒性T淋巴细胞(CTL)。本II期试验的目的是研究KRM-20联合多西紫杉醇和地塞米松是否能增强去势耐受性前列腺癌(CRPC)患者的抗肿瘤作用。在这项双盲、安慰剂对照、随机II期研究中,我们从日本十个医疗中心招募了未接受化疗的CRPC患者。合格患者按1:1的比例随机分为两组,一组接受KRM-20联合多西紫杉醇和地塞米松治疗(n=25),另一组接受安慰剂联合多西紫杉醇和地塞米松治疗(n=26)。主要终点是每种治疗之间前列腺特异性抗原(PSA)下降的差异。两组PSA下降>50%的比率相似(56.5%对53.8%;P=0.851)。KRM-20组的人类白细胞抗原(HLA)匹配肽特异性免疫球蛋白G(P=0.018)和CTL(P=0.007)反应在治疗后显著增加。添加KRM-20不会增加毒性。组间无进展生存率或总生存率(OS)无差异。在CRPC患者中,加入KRM-20是安全的,与多西紫杉醇和地塞米松联合使用时,PSA下降和HLA匹配的肽特异性CTL和IgG反应增加。亚组分析表明,这种治疗对淋巴细胞>26%或PSA水平<11.2 ng/ml的CRPC患者有利,但还需要进一步的临床试验来比较OS。

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