Department of Radiology, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, Massachusetts.
Department of Biostatistics, Dana-Farber Cancer Institute, Boston, Massachusetts.
Clin Cancer Res. 2017 Oct 1;23(19):5737-5744. doi: 10.1158/1078-0432.CCR-17-1434. Epub 2017 Jul 5.
We evaluated tumor burden dynamics in patients with advanced non-small cell lung cancer (NSCLC) treated with commercial PD-1 inhibitors to identify imaging markers associated with improved overall survival (OS). The study included 160 patients with advanced NSCLC treated with commercial nivolumab or pembrolizumab monotherapy as a part of clinical care. Tumor burden dynamics were studied for the association with OS. Tumor burden change at best overall response (BOR) ranged from -100% to +278% (median, +3.5%). Response rate (RR) was 18% (29/160). Current and former smokers had a higher RR than never smokers ( = 0.04). Durable disease control for at least 6 months was noted in 26 patients (16%), which included 10 patients with stable disease as BOR. Using a landmark analysis, patients with <20% tumor burden increase from baseline within 8 weeks of therapy had longer OS than patients with ≥20% increase (median OS, 12.4 vs. 4.6 months, < 0.001). Patients with <20% tumor burden increase throughout therapy had significantly reduced hazards of death (HR, 0.24; Cox < 0.0001) after adjusting for smoking (HR, 0.86; = 0.61) and baseline tumor burden (HR, 1.55; = 0.062), even though some patients met criteria for RECIST progression while on therapy. One patient (0.6%) had atypical response pattern consistent with pseudoprogression. Objective response or durable disease control was noted in 24% of patients with advanced NSCLC treated with commercial PD-1 inhibitors. A tumor burden increase of <20% from baseline during therapy was associated with longer OS, proposing a practical marker of treatment benefit. Pseudoprogression is rare in NSCLCs treated with PD-1 inhibitors. .
我们评估了接受商业 PD-1 抑制剂治疗的晚期非小细胞肺癌(NSCLC)患者的肿瘤负担动态变化,以确定与总生存期(OS)改善相关的影像学标志物。该研究纳入了 160 例接受商业纳武利尤单抗或帕博利珠单抗单药治疗的晚期 NSCLC 患者,这些患者的治疗均为临床常规。研究了肿瘤负担变化与 OS 的关系。最佳总缓解(BOR)时的肿瘤负担变化范围为-100%至+278%(中位数,+3.5%)。缓解率(RR)为 18%(29/160)。当前和曾经吸烟者的 RR 高于从不吸烟者(=0.04)。26 例(16%)患者至少有 6 个月的疾病稳定,其中包括 10 例 BOR 为稳定疾病的患者。采用 landmark 分析,在治疗 8 周内肿瘤负荷较基线增加<20%的患者 OS 长于增加≥20%的患者(中位 OS,12.4 与 4.6 个月,<0.001)。在整个治疗过程中肿瘤负荷增加<20%的患者,在校正吸烟(HR,0.86;=0.61)和基线肿瘤负荷(HR,1.55;=0.062)后,死亡风险显著降低(HR,0.24;Cox<0.0001),尽管一些患者在治疗期间符合 RECIST 进展标准。1 例(0.6%)患者出现符合假性进展的非典型反应模式。接受商业 PD-1 抑制剂治疗的晚期 NSCLC 患者中,有 24%观察到客观缓解或疾病稳定。治疗过程中肿瘤负荷较基线增加<20%与 OS 延长相关,提示治疗获益的实用标志物。PD-1 抑制剂治疗的 NSCLC 中很少出现假性进展。