Noguchi Masanori, Moriya Fukuko, Koga Noriko, Matsueda Satoko, Sasada Tetsuro, Yamada Akira, Kakuma Tatsuyuki, Itoh Kyogo
Division of Clinical Research, Research Center for Innovative Cancer Therapy, Kurume University School of Medicine, Kurume, Japan.
Department of Urology, Kurume University School of Medicine, 67 Asahi-machi, Kurume, 830-0011, Japan.
Cancer Immunol Immunother. 2016 Feb;65(2):151-60. doi: 10.1007/s00262-015-1781-6. Epub 2016 Jan 4.
This study investigated the effect of metronomic cyclophosphamide (CPA) in combination with personalized peptide vaccination (PPV) on regulatory T cells (Treg) and myeloid-derived suppressor cells (MDSC), and whether it could improve the antitumor effect of PPV. Seventy patients with metastatic castration-resistant prostate cancer were randomly assigned (1:1) to receive PPV plus oral low-dose CPA (50 mg/day), or PPV alone. PPV treatment used a maximum of four peptides chosen from 31 pooled peptides according to human leukocyte antigen types and antigen-specific humoral immune responses before PPV, for 8 subcutaneous weekly injections. Peptide-specific cytotoxic T lymphocyte (CTL) and immunoglobulin G responses were measured before and after PPV. The incidence of grade 3 or 4 hematologic adverse events was higher in the PPV plus CPA arm than in the PPV alone arm. Decrease in Treg and increase in MDSC were more pronounced in PPV plus CPA treatment than in PPV alone (p = 0.036 and p = 0.048, respectively). There was no correlation between the changes in Treg or MDSC and CTL response. There was no difference in positive immune responses between the two arms, although overall survival in patients with positive immune responses was longer than in those with negative immune responses (p = 0.001). Significant differences in neither progression-free survival nor overall survival were observed between the two arms. Low-dose CPA showed no change in the antitumor effect of PPV, possibly due to the simultaneous decrease in Treg and increase in MDSC, in patients under PPV.
本研究调查了节拍性环磷酰胺(CPA)联合个性化肽疫苗接种(PPV)对调节性T细胞(Treg)和髓源性抑制细胞(MDSC)的影响,以及其是否能提高PPV的抗肿瘤效果。70例转移性去势抵抗性前列腺癌患者被随机分配(1:1)接受PPV加口服低剂量CPA(50毫克/天),或单独接受PPV。PPV治疗根据人类白细胞抗原类型和PPV前的抗原特异性体液免疫反应,从31种混合肽中最多选择4种肽,每周皮下注射8次。在PPV前后测量肽特异性细胞毒性T淋巴细胞(CTL)和免疫球蛋白G反应。PPV加CPA组3级或4级血液学不良事件的发生率高于单独PPV组。与单独PPV治疗相比,PPV加CPA治疗中Treg的减少和MDSC的增加更为明显(分别为p = 0.036和p = 0.048)。Treg或MDSC的变化与CTL反应之间没有相关性。两组之间的阳性免疫反应没有差异,尽管阳性免疫反应患者的总生存期长于阴性免疫反应患者(p = 0.001)。两组之间在无进展生存期和总生存期方面均未观察到显著差异。低剂量CPA在接受PPV的患者中未显示出对PPV抗肿瘤效果的改变,这可能是由于Treg同时减少和MDSC增加所致。