Department of Surgery, Kurume University School of Medicine, Kurume, Japan.
Cancer Sci. 2012 Apr;103(4):638-44. doi: 10.1111/j.1349-7006.2012.02202.x. Epub 2012 Feb 13.
Since the prognosis of small cell lung cancer (SCLC) remains poor, development of new therapeutic approaches, including immunotherapies, would be desirable. In the current study, to evaluate immunological responses in refractory SCLC patients, we conducted a small scale phase II clinical trial of personalized peptide vaccination (PPV), in which vaccine antigens are selected based on pre-existing host immunity. Ten refractory SCLC patients, who had failed to respond to chemo- and/or chemoradiotherapies (median number of regimens, 2.5; median duration, 20.5 months), were enrolled. A maximum of four human leukocyte antigen (HLA)-matched peptides showing higher antigen-specific humoral responses were subcutaneously administered (weekly for six consecutive weeks and then bi-weekly thereafter). PPV was terminated before the 3rd administration in four patients because of rapid disease progression, whereas the remaining six patients completed at least one cycle (six times) of vaccinations. Peptide-specific immunological boosting was observed in all of the six patients at the end of the first cycle of vaccinations, with their survival time of 25, 24.5 (alive), 10 (alive), 9.5, 6.5, and 6 months. Number of previous chemotherapy regimens and frequency of CD3(+) CD26(+) cells in peripheral blood were potentially prognostic in the vaccinated patients (hazard ratio [HR] = 2.540, 95% confidence interval [CI] = 1.188-5.431, P = 0.016; HR = 0.941, 95% CI = 0.878-1.008, P = 0.084; respectively). Based on the feasible immune responses in refractory SCLC patients who received at least one cycle (six times) of vaccinations, PPV could be recommended for a next stage of larger-scale, prospective clinical trials.
由于小细胞肺癌 (SCLC) 的预后仍然较差,因此需要开发新的治疗方法,包括免疫疗法。在目前的研究中,为了评估难治性 SCLC 患者的免疫反应,我们进行了一项小规模的 II 期临床试验,即个体化肽疫苗接种 (PPV),其中疫苗抗原是根据宿主预先存在的免疫反应选择的。纳入了 10 名对化疗和/或放化疗无反应的难治性 SCLC 患者(化疗方案中位数为 2.5 个,中位持续时间为 20.5 个月)。最多可以皮下注射四种与人类白细胞抗原 (HLA) 匹配的肽,这些肽显示出更高的抗原特异性体液反应(连续 6 周每周一次,然后此后每两周一次)。由于疾病快速进展,有 4 名患者在第 3 次给药前终止了 PPV,而其余 6 名患者至少完成了一个周期(6 次)的疫苗接种。在第一个周期的疫苗接种结束时,所有 6 名患者都观察到了肽特异性免疫增强,他们的生存时间分别为 25、24.5(存活)、10(存活)、9.5、6.5 和 6 个月。既往化疗方案的数量和外周血中 CD3(+) CD26(+)细胞的频率可能与接种疫苗的患者的预后有关(风险比 [HR] = 2.540,95%置信区间 [CI] = 1.188-5.431,P = 0.016;HR = 0.941,95%CI = 0.878-1.008,P = 0.084;分别)。基于至少接受一个周期(6 次)接种的难治性 SCLC 患者可行的免疫反应,PPV 可推荐用于下一阶段更大规模的前瞻性临床试验。