1 Department of Pulmonary Medicine and.
2 Department of Cardio-Thoracic Surgery, Erasmus MC Cancer Institute, Rotterdam, the Netherlands; and.
Am J Respir Crit Care Med. 2016 May 1;193(9):1023-31. doi: 10.1164/rccm.201508-1573OC.
We demonstrated previously that autologous tumor lysate-pulsed dendritic cell-based immunotherapy in patients with malignant pleural mesothelioma is feasible, well-tolerated, and capable of inducing immunologic responses against tumor cells. In our murine model, we found that reduction of regulatory T cells with metronomic cyclophosphamide increased the efficacy of immunotherapy.
To assess the decrease in number of peripheral blood regulatory T cells during combination therapy of low-dose cyclophosphamide and dendritic cell immunotherapy and determine the induction of immunologic responses with this treatment in patients with mesothelioma.
Ten patients with malignant pleural mesothelioma received metronomic cyclophosphamide and dendritic cell-based immunotherapy. During the treatment, peripheral blood mononuclear cells were analyzed for regulatory T cells and immunologic responses.
Administration of dendritic cells pulsed with autologous tumor lysate combined with cyclophosphamide in patients with mesothelioma was safe, the only side effect being moderate fever. Dendritic cell vaccination combined with cyclophosphamide resulted in radiographic disease control in 8 of the 10 patients. Overall survival was promising, with 7 out of 10 patients having a survival of greater than or equal to 24 months and two patients still alive after 50 and 66 months. Low-dose cyclophosphamide reduced the percentage of regulatory T cells of total CD4 cells in peripheral blood from 9.43 (range, 4.34-26.10) to 4.51 (range, 0.27-10.30) after 7 days of cyclophosphamide treatment (P = 0.02).
Consolidation therapy with autologous tumor lysate-pulsed dendritic cell-based therapy and simultaneously reducing the tumor-induced immune suppression is well-tolerated and shows signs of clinical activity in patients with mesothelioma. Clinical trial registered with www.clinicaltrials.gov (NCT 01241682).
我们之前已经证明,自体肿瘤裂解物脉冲树突状细胞免疫疗法在恶性胸膜间皮瘤患者中是可行的、耐受良好的,并且能够诱导针对肿瘤细胞的免疫反应。在我们的小鼠模型中,我们发现用低剂量环磷酰胺减少调节性 T 细胞可以提高免疫治疗的效果。
评估低剂量环磷酰胺和树突状细胞免疫治疗联合治疗期间外周血调节性 T 细胞数量的减少,并确定这种治疗方法在间皮瘤患者中诱导免疫反应的情况。
10 名恶性胸膜间皮瘤患者接受了低剂量环磷酰胺和树突状细胞免疫治疗。在治疗过程中,分析外周血单核细胞中的调节性 T 细胞和免疫反应。
在间皮瘤患者中,自体肿瘤裂解物脉冲树突状细胞联合环磷酰胺的治疗是安全的,唯一的副作用是中度发热。树突状细胞疫苗接种联合环磷酰胺治疗使 10 名患者中的 8 名患者的疾病得到了影像学控制。总生存率很有希望,10 名患者中有 7 名患者的生存时间大于或等于 24 个月,2 名患者在 50 个月和 66 个月后仍存活。低剂量环磷酰胺治疗 7 天后,外周血中调节性 T 细胞占总 CD4 细胞的百分比从 9.43(范围,4.34-26.10)降至 4.51(范围,0.27-10.30)(P=0.02)。
自体肿瘤裂解物脉冲树突状细胞治疗联合治疗和同时减少肿瘤诱导的免疫抑制是耐受良好的,并在间皮瘤患者中显示出临床活性的迹象。该临床试验已在 www.clinicaltrials.gov 注册(NCT 01241682)。