UC Davis Health, Sacramento, CA, 95817, USA.
Cedars-Sinai Medical Center, Los Angeles, CA, 90048, USA.
Nat Commun. 2023 Sep 2;14(1):5332. doi: 10.1038/s41467-023-40813-w.
Stereotactic ablative radiotherapy (SABR) is a standard-of-care for medically-inoperable-early-stage non-small cell lung cancer (NSCLC). One third of patients progress and chemotherapy is rarely used in this population. We questioned if addition of the immune-checkpoint-inhibitor (ICI) atezolizumab to standard-of-care SABR can improve outcomes. We initiated a multi-institutional single-arm phase I study (NCT02599454) enrolling twenty patients with the primary endpoint of maximum tolerated dose (MTD); secondary endpoints of safety and efficacy; and exploratory mechanistic correlatives. Treatment is well tolerated and full dose atezolizumab (1200 mg) is the MTD. Efficacy signals include early responses (after 2 cycles of ICI, before initiation of SABR) in 17% of patients. Biomarkers of functional adaptive immunity, including T cell activation in the tumor and response to ex-vivo stimulation by circulating T cells, are highly predictive of benefit. These results require validation and are being tested in a phase III randomized trial.
立体定向消融放疗 (SABR) 是不可手术的早期非小细胞肺癌 (NSCLC) 的标准治疗方法。三分之一的患者会出现进展,而在这一人群中很少使用化疗。我们质疑在标准 SABR 治疗的基础上加入免疫检查点抑制剂 (ICI) atezolizumab 是否可以改善预后。我们启动了一项多机构单臂 I 期研究 (NCT02599454),入组了 20 名患者,主要终点是最大耐受剂量 (MTD);次要终点是安全性和疗效;以及探索性的机制相关性。治疗耐受性良好,全剂量 atezolizumab(1200mg)是 MTD。疗效信号包括 17%的患者在 ICI 治疗 2 个周期后(在开始 SABR 之前)出现早期反应。肿瘤中 T 细胞激活和循环 T 细胞对外源性刺激的反应等功能性适应性免疫生物标志物高度预测获益。这些结果需要验证,并正在一项 III 期随机试验中进行测试。