Johns Hopkins Kimmel Cancer Center, Baltimore, MD 21231, USA.
Ann Oncol. 2012 Sep;23 Suppl 8(Suppl 8):viii41-6. doi: 10.1093/annonc/mds262.
Combination immunotherapy approaches involving radiation, chemotherapy, androgen manipulation and T-cell modulation have been studied extensively in animal models, setting the stage for clinical trials. Radiation therapy, in particular, is an interesting modality in this regard, leading to synergistic efficacy when used in combination with immunotherapies in several models. Chemotherapy, the foundation of treatment of metastatic disease, may also augment the immune response to cancer; however, the potential immunosuppressive effects of chemotherapy render issues of dosing and timing critical. Perhaps, the most exciting combinatorial approach may be the co-administration of multiple immunological treatments. For example, in preclinical investigations, combined blockade of programmed death-1 (PD1) and cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), which have key roles in the negative regulation of T-cell activation, has been shown to enhance antitumour immune responses compared with either agent alone. Taken together, the available data provide a strong rationale for initiating combination clinical trials, but lend a note of caution in that issues of dosing and timing likely require careful exploration in a phase II setting.
联合免疫疗法包括放疗、化疗、雄激素处理和 T 细胞调节,已在动物模型中广泛研究,为临床试验奠定了基础。特别是放疗在这方面是一种很有趣的治疗方法,在几种模型中与免疫疗法联合使用时具有协同疗效。化疗是治疗转移性疾病的基础,也可能增强对癌症的免疫反应;然而,化疗的潜在免疫抑制作用使得剂量和时间成为关键问题。也许,最令人兴奋的联合治疗方法可能是同时使用多种免疫治疗方法。例如,在临床前研究中,程序性死亡受体 1(PD1)和细胞毒性 T 淋巴细胞相关抗原 4(CTLA-4)的联合阻断,它们在 T 细胞激活的负调节中起关键作用,与单独使用任何一种药物相比,都能增强抗肿瘤免疫反应。综上所述,现有数据为启动联合临床试验提供了强有力的理由,但也提醒我们,剂量和时间问题可能需要在 II 期临床试验中仔细探索。