Gangadhar Tara C, Salama April Ks
Division of Hematology/Oncology, Department of Medicine, Abramson Cancer Center of the University of Pennsylvania, Philadelphia, PA, USA.
Division of Medical Oncology, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Onco Targets Ther. 2015 Apr 22;8:929-37. doi: 10.2147/OTT.S53164. eCollection 2015.
Preclinical work has led to an increased understanding of the immunomodulatory mechanisms involved in the regulation of the antitumor response in a variety of tumor types. PD-1 (programmed death 1) appears to be a key checkpoint involved in immune suppression in the tumor microenvironment, even in diseases not previously thought to be sensitive to immune manipulation. More recently, the subsequent clinical development of PD-1-based therapy has resulted in a major breakthrough in the field of oncology. Pembrolizumab, a humanized highly selective IgG4 anti-PD-1 monoclonal antibody, was recently approved for the treatment of advanced melanoma based on promising early-phase clinical data. Encouraging results have also been seen in other malignancies, and PD-1-targeted therapies are likely to markedly change the treatment landscape. Future work will center on rationally designed combination strategies in order to potentiate the antitumor immune response and overcome mechanisms of resistance.
临床前研究工作增进了我们对多种肿瘤类型中抗肿瘤反应调节所涉及的免疫调节机制的理解。PD-1(程序性死亡蛋白1)似乎是肿瘤微环境中免疫抑制所涉及的关键检查点,即使在以前认为对免疫调控不敏感的疾病中也是如此。最近,基于PD-1的疗法随后的临床开发在肿瘤学领域取得了重大突破。帕博利珠单抗是一种人源化的高选择性IgG4抗PD-1单克隆抗体,基于有前景的早期临床数据,最近被批准用于治疗晚期黑色素瘤。在其他恶性肿瘤中也观察到了令人鼓舞的结果,并且靶向PD-1的疗法可能会显著改变治疗格局。未来的工作将集中在合理设计联合策略上,以增强抗肿瘤免疫反应并克服耐药机制。