Department of Urology, Kinki University School of Medicine, Osaka-Sayama, Osaka, Japan.
Cancer Sci. 2010 Mar;101(3):601-8. doi: 10.1111/j.1349-7006.2009.01459.x. Epub 2009 Dec 7.
We previously reported that personalized peptide vaccine (PPV) therapy in combination with leutenizing hormone-releasing hormone (LH-RH) analog and estramustine phosphate in certain cases is safe and capable of inducing both immune responses and clinical responses for metastatic castration-resistant prostate cancer (CRPC) patients. In the present study, PPV monotherapy was given to CRPC patients. Twenty-three patients with metastatic CRPC were treated with PPV without any additional treatment modalities, including LH-RH analogs. Samples were analyzed for peptide-specific cytotoxic T-lymphocyte (CTL) precursor analysis and peptide-reactive IgG. Toxicity and immunological and clinical responses were assessed on a three-monthly basis. Seventeen patients were available for immunological and clinical evaluation. The vaccines were well tolerated, with grade 3 erythema at injection sites in only one patient. Augmentation of CTL or IgG responses to at least one of the peptides was observed in six of 17 (35%) and 15 of 17 (88%) patients tested, respectively. Among 57 peptides used, 9 and 36 peptides induced CTL and IgG responses, respectively. Delayed-type hypersensitivity reaction was observed in eight of 17 patients. More than 30% prostate-specific antigen (PSA) decline was observed in four of 17 patients. Of these, one patient achieved a complete PSA response and another patient showed a partial PSA response with profound shrinking of lymph node metastases and prostate. The overall median survival time was 24 months (range, 5-37 months). These results suggest that PPV monotherapy appears to be safe and capable of inducing peptide-specific immune responses and clinical responses in CRPC patients. This trial was registered with University Hospital Medical Information Network (UMIN) number R000003339.
我们之前报道过,在某些情况下,个性化肽疫苗(PPV)联合促黄体激素释放激素(LH-RH)类似物和磷酸雌莫司汀治疗转移性去势抵抗性前列腺癌(CRPC)患者是安全的,能够诱导免疫和临床反应。在本研究中,我们对 CRPC 患者进行了 PPV 单药治疗。23 例转移性 CRPC 患者接受了 PPV 治疗,未使用任何其他治疗方法,包括 LH-RH 类似物。分析了样本中的肽特异性细胞毒性 T 淋巴细胞(CTL)前体分析和肽反应性 IgG。每三个月评估一次毒性、免疫和临床反应。17 例患者可进行免疫和临床评估。疫苗耐受性良好,仅有 1 例患者注射部位出现 3 级红斑。在 17 例可检测的患者中,分别有 6 例(35%)和 15 例(88%)患者对至少一种肽的 CTL 或 IgG 反应增强。在使用的 57 种肽中,分别有 9 种和 36 种肽诱导了 CTL 和 IgG 反应。17 例患者中有 8 例观察到迟发型超敏反应。17 例患者中有 4 例 PSA 下降超过 30%。其中,1 例患者达到完全 PSA 缓解,另 1 例患者 PSA 部分缓解,淋巴结转移和前列腺明显缩小。总体中位生存时间为 24 个月(范围为 5-37 个月)。这些结果表明,PPV 单药治疗似乎是安全的,能够诱导 CRPC 患者产生肽特异性免疫和临床反应。该试验在大学医院医疗信息网络(UMIN)注册,注册号为 R000003339。