Hematology Oncology Fellowship Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Cancer Control. 2013 Jan;20(1):22-31. doi: 10.1177/107327481302000105.
Lung cancer is the most common cause of cancer-related death in the United States, yet traditional chemotherapy fails to provide long-term benefit for many patients. New approaches are needed to improve overall survival beyond the current standard of care.
This review discusses recent clinical trials using immunotherapy techniques to treat both non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) and highlights ongoing immunotherapy research efforts at our center.
For NSCLC, phase II clinical trials have examined allogeneic vaccines that target either mucin 1 (MUC1), epidermal growth factor or melanoma-associated antigen 3. These vaccines are now undergoing larger phase III trials. An autologous cellular therapy directed against transforming growth factor beta-2 and a recombinant protein with antitumor properties have also shown promise in prolonging survival in NSCLC in phase II trials. The monoclonal antibodies ipilimumab, BMS-936558 (anti-PD-1), and BMS936559 (anti-PD-L1) lead to enhanced T-cell-mediated antitumor effects and have produced objective responses in early-phase clinical trials. Studies for SCLC also exist, such as a novel vaccine therapy targeting p53.
Recent clinical trials in lung cancer demonstrate the potential of immunotherapeutics to increase overall survival in patients with lung cancer compared with the current standard of care.
肺癌是美国癌症相关死亡的最常见原因,但传统化疗未能为许多患者提供长期获益。需要新的方法来改善整体生存,超越当前的护理标准。
本综述讨论了最近使用免疫疗法治疗非小细胞肺癌(NSCLC)和小细胞肺癌(SCLC)的临床试验,并强调了我们中心正在进行的免疫疗法研究工作。
对于 NSCLC,二期临床试验已经检查了针对粘蛋白 1(MUC1)、表皮生长因子或黑色素瘤相关抗原 3 的同种异体疫苗。这些疫苗现在正在进行更大的三期试验。针对转化生长因子β-2 的自体细胞疗法和具有抗肿瘤特性的重组蛋白也在二期试验中显示出延长 NSCLC 生存的潜力。单克隆抗体 ipilimumab、BMS-936558(抗 PD-1)和 BMS936559(抗 PD-L1)导致增强的 T 细胞介导的抗肿瘤作用,并在早期临床试验中产生了客观反应。SCLC 的研究也存在,例如针对 p53 的新型疫苗疗法。
肺癌的最近临床试验表明,与当前的护理标准相比,免疫疗法有可能增加肺癌患者的总体生存率。