Joshi Shweta, Durden Donald L
Division of Pediatric Hematology-Oncology, Department of Pediatrics, Moores Cancer Center, University of California, San Diego, CA, USA.
SignalRx Pharmaceuticals, Inc., San Diego, CA, USA.
J Oncol. 2019 Feb 3;2019:5245034. doi: 10.1155/2019/5245034. eCollection 2019.
Cancer immunotherapy, including immune checkpoint blockade and adoptive CAR T-cell therapy, has clearly established itself as an important modality to treat melanoma and other malignancies. Despite the tremendous clinical success of immunotherapy over other cancer treatments, this approach has shown substantial benefit to only some of the patients while the rest of the patients have not responded due to immune evasion. In recent years, a combination of cancer immunotherapy together with existing anticancer treatments has gained significant attention and has been extensively investigated in preclinical or clinical studies. In this review, we discuss the therapeutic potential of novel regimens combining immune checkpoint inhibitors with therapeutic interventions that (1) increase tumor immunogenicity such as chemotherapy, radiotherapy, and epigenetic therapy; (2) reverse tumor immunosuppression such as TAMs, MDSCs, and Tregs targeted therapy; and (3) reduce tumor burden and increase the immune effector response with rationally designed dual or triple inhibitory chemotypes.
癌症免疫疗法,包括免疫检查点阻断和过继性嵌合抗原受体(CAR)T细胞疗法,已明确确立其作为治疗黑色素瘤和其他恶性肿瘤的重要方式。尽管免疫疗法相较于其他癌症治疗方法取得了巨大的临床成功,但这种方法仅对部分患者显示出显著益处,而其余患者由于免疫逃逸未产生反应。近年来,癌症免疫疗法与现有抗癌治疗方法的联合应用受到了广泛关注,并在临床前或临床研究中得到了广泛研究。在本综述中,我们讨论了将免疫检查点抑制剂与以下治疗干预措施相结合的新型方案的治疗潜力:(1)增加肿瘤免疫原性的措施,如化疗、放疗和表观遗传疗法;(2)逆转肿瘤免疫抑制的措施,如针对肿瘤相关巨噬细胞(TAM)、骨髓来源的抑制性细胞(MDSC)和调节性T细胞(Treg)的靶向治疗;以及(3)通过合理设计的双重或三重抑制化学类型减轻肿瘤负担并增强免疫效应反应。