Suppr超能文献

混合 20 肽癌症疫苗联合多西他赛和地塞米松治疗去势抵抗性前列腺癌:一项随机 II 期试验。

Mixed 20-peptide cancer vaccine in combination with docetaxel and dexamethasone for castration-resistant prostate cancer: a randomized phase II trial.

机构信息

Canver Vaccine Center, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan.

Department of Urology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan.

出版信息

Cancer Immunol Immunother. 2020 May;69(5):847-857. doi: 10.1007/s00262-020-02498-8. Epub 2020 Feb 5.

Abstract

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.

摘要

一种由 20 种混合肽(KRM-20)组成的新型癌症疫苗旨在诱导针对 12 种不同肿瘤相关抗原的细胞毒性 T 淋巴细胞(CTL)。这项 II 期试验的目的是研究 KRM-20 联合多西他赛和地塞米松是否能增强去势抵抗性前列腺癌(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,我们从日本的 10 个医学中心招募了化疗初治的 CRPC 患者。符合条件的患者被中央随机分配 1:1 接受 KRM-20 联合多西他赛和地塞米松(n=25)或安慰剂联合多西他赛和地塞米松(n=26)。主要终点是每个治疗组前列腺特异性抗原(PSA)下降的差异。两个治疗组中 PSA 下降超过 50%的比例相似(56.5%与 53.8%;P=0.851)。KRM-20 组 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 并未增加毒性。无进展生存期和总生存期(OS)无组间差异。添加 KRM-20 是安全的,与多西他赛和地塞米松联合使用时,CRPC 患者的 PSA 下降和 HLA 匹配肽特异性 CTL 和 IgG 反应相似增加。亚组分析表明,这种治疗对淋巴细胞≥26%或 PSA 水平<11.2ng/ml 的 CRPC 患者有利,但需要进行比较 OS 的进一步临床试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3947/11027807/3c0447937d74/262_2020_2498_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验