Sakamoto Shinjiro, Yutani Shigeru, Shichijo Shigeki, Morita Michi, Yamada Akira, Itoh Kyogo, Noguchi Masanori
Cancer Vaccine Center, Research Center for Innovative Cancer Therapy, Kurume University School of Medicine, Kurume, Japan.
Clinical Research Division, Research Center for Innovative Cancer Therapy, Kurume University School of Medicine, 67 Asahi-Machi, Kurume, 830-0011, Japan.
Cancer Immunol Immunother. 2016 Oct;65(10):1223-31. doi: 10.1007/s00262-016-1887-5. Epub 2016 Aug 22.
The immunological characteristics of carcinoma of unknown primary site (CUP) are not well established due to inclusion of heterogeneous types of metastatic tumors with the absence of any detectable primary site. We evaluated the immune responses in patients with histologically unfavorable CUP during personalized peptide vaccination (PPV). Ten patients with histologically unfavorable CUP who had been treated by PPV after chemotherapy failure were analyzed. In PPV treatment, up to four human leukocyte antigen-matched peptides of a total 31 peptides were selected according to preexisting host immunity before vaccination and administered subcutaneously. Peptides derived from the Lck antigen were most often chosen for use among all patients. CTL responses were increased in 8 of the 10 and 5 of the five patients tested at the end of the first and second PPV cycles, respectively. Increases in humoral responses after vaccination, including IgG, IgG1, IgG3, IgA, and IgM, were observed against not only the vaccinated peptides but also the non-vaccinated peptides. Severe adverse events due to PPV were not observed. Median overall survival was 13.9 months (95 % CI 4.0-22.5 months). PPV activated both cellular and humoral immune responses to short peptides derived from CTL epitopes in the majority of CUP patients. PPV with Lck-derived peptides may be a feasible, new treatment modality for histologically unfavorable CUP patients due to its safety and strong ability to boost immune responses, although its clinical efficacy remains to be investigated in larger-scale trials.
由于原发性不明癌(CUP)包含异质性转移瘤类型且未发现任何可检测的原发部位,其免疫特征尚未完全明确。我们评估了组织学上预后不良的CUP患者在个性化肽疫苗接种(PPV)期间的免疫反应。分析了10例化疗失败后接受PPV治疗的组织学预后不良的CUP患者。在PPV治疗中,根据接种前宿主的已有免疫力,从总共31种肽中选择多达4种与人类白细胞抗原匹配的肽,并进行皮下注射。在所有患者中,最常选用源自Lck抗原的肽。在第一个和第二个PPV周期结束时,分别对10例患者中的8例和5例患者进行检测,发现细胞毒性T淋巴细胞(CTL)反应增强。接种疫苗后体液反应增强,包括IgG、IgG1、IgG3、IgA和IgM,不仅针对接种的肽,也针对未接种的肽。未观察到PPV引起的严重不良事件。中位总生存期为13.9个月(95%可信区间4.0 - 22.5个月)。PPV在大多数CUP患者中激活了针对源自CTL表位的短肽的细胞免疫和体液免疫反应。尽管其临床疗效仍有待在更大规模试验中研究,但含Lck衍生肽的PPV因其安全性和强大的免疫反应增强能力,可能是一种针对组织学预后不良的CUP患者可行的新治疗方式。