Drug Development Department (DITEP), Gustave Roussy, Saclay University of Paris, Villejuif, France.
Oncology Department, Clínica Universidad de Navarra, Madrid, Spain.
Cancer Med. 2020 Apr;9(8):2643-2652. doi: 10.1002/cam4.2797. Epub 2020 Feb 19.
PD(L)1 antibodies (anti-PD(L)-1) have been a major breakthrough in several types of cancer. Novel patterns of response and progression have been described with anti-PD(L)-1. We aimed at characterizing pseudoprogression (PSPD) among patients with various solid tumor types treated by anti-PD(L)-1.
All consecutive patients (pts) enrolled in phase 1 trials with advanced solid tumors and lymphomas treated in phase I clinical trials evaluating monotherapy by anti-PD(L)-1 at Gustave Roussy were analyzed. We aimed to assess prevalence and outcome of PSPD across tumor types. We also intended to describe potential clinical and pathological factors associated with PSPD.
A total of 169 patients treated with anti-PD(L)-1 were included in the study. Most frequent tumor types included melanoma (n = 57) and non-small cell lung cancer (n = 19). At first tumor evaluation 77 patients (46%) presented with immune unconfirmed progressive disease. Six patients (8%) experienced PSPD: 2 patients with partial response; 4 patients with stable disease. Increase in target lesions in the first CT-scan was more frequently associated to PSPD (67% vs 33%; P = .04). Patients with a PSPD had a superior survival when compared to patients progressing (median OS: 10.7 months vs 8.7 months; P = .07).
A small subset of PSPD patients may experience response after an initial progression. Assessment of the current strategy for immune-related response evaluations may require further attention.
PD(L)1 抗体(抗 PD(L)-1)在多种癌症中取得了重大突破。已有研究描述了抗 PD(L)-1 治疗时新的反应和进展模式。我们旨在描述各种实体瘤类型的患者接受抗 PD(L)-1 治疗时出现的假性进展(PSPD)。
所有连续入组的晚期实体瘤和淋巴瘤患者,均接受了 Gustave Roussy 进行的 I 期临床试验中评估的抗 PD(L)-1 单药治疗。我们旨在评估不同肿瘤类型中 PSPD 的发生率和结局。我们还打算描述与 PSPD 相关的潜在临床和病理因素。
共有 169 例接受抗 PD(L)-1 治疗的患者纳入了本研究。最常见的肿瘤类型包括黑色素瘤(n=57)和非小细胞肺癌(n=19)。在首次肿瘤评估时,77 例患者(46%)表现为免疫未确认的进展性疾病。6 例患者(8%)发生了 PSPD:2 例部分缓解,4 例病情稳定。首次 CT 扫描中靶病灶增加更常与 PSPD 相关(67% vs 33%;P=0.04)。与进展患者相比,PSPD 患者的生存时间更优(中位 OS:10.7 个月 vs 8.7 个月;P=0.07)。
一小部分 PSPD 患者在初始进展后可能会出现缓解。可能需要进一步关注目前免疫相关反应评估策略的评估。