Chen Xin, Lim-Fat Mary Jane, Qin Lei, Li Angie, Bryant Annie, Bay Camden P, Gao Lu, Miskin Nityanand, Liu Zaiyi, Iorgulescu J Bryan, Xu Xiaoyin, Reardon David A, Young Geoffrey S
Department of Radiology, Brigham and Women's Hospital, Boston, MA, United States.
Department of Radiology, Guangzhou First People's Hospital, The Second Affiliated Hospital of South China University of Technology, Guangzhou, China.
Front Oncol. 2021 Jun 25;11:679331. doi: 10.3389/fonc.2021.679331. eCollection 2021.
Real-time assessment of treatment response in glioblastoma (GBM) patients on immune checkpoint blockade (ICB) remains challenging because inflammatory effects of therapy may mimic progressive disease, and the temporal evolution of these inflammatory findings is poorly understood. We compare GBM patient response during ICB as assessed with the Immunotherapy Response Assessment in Neuro-Oncology (iRANO) and the standard Response Assessment in Neuro-Oncology (RANO) radiological criteria.
49 GBM patients (seven newly diagnosed and 42 recurrent) treated with ICBs at a single institution were identified. Tumor burden was quantified on serial MR scans according to RANO criteria during ICB. Radiographic response assessment by iRANO and RANO were compared.
82% (40/49) of patients received anti-PD-1, 16% (8/49) received anti-PD-L1, and 2% (1/49) received anti-PD-1 and anti-CTLA4 treatment. Change in tumor burden and best overall response ranged from -100 to +557% (median: +48%). 12% (6/49) of patients were classified as concordant non-progressors by both RANO and iRANO (best response: one CR, one PR, and four SD). Another12% (6/49) had discordant assessments: 15% (6/41) of RANO grade progressive disease (PD) patients had iRANO grade of progressive disease unconfirmed (PDU). The final classification of these discordant patients was pseudoprogression (PsP) in three of six, PD in two of six, and PDU in one of six who went off study before the iRANO assessment of PDU. iRANO delayed diagnosis of PD by 42 and 93 days in the two PD patients. 76% (37/49) patients were classified as concordant PD by both RANO and iRANO. 12% (6/49) of all patients were classified as PsP, starting at a median of 12 weeks (range, 4-30 weeks) after ICB initiation.
Standard RANO and iRANO have high concordance for assessing PD in patients within 6 months of ICB initiation. iRANO was beneficial in 6% (3/49) cases later proven to be PsP, but delayed confirmation of PD by <3 months in 4% (2/49). PsP occurred in 12% of patients, starting at up to 7 months after initiation of ICB. Further study to define the utility of modified RANO compared with iRANO in ICB GBM patients is needed.
胶质母细胞瘤(GBM)患者接受免疫检查点阻断(ICB)治疗时,对治疗反应的实时评估仍然具有挑战性,因为治疗的炎症效应可能会模仿疾病进展,而且这些炎症表现的时间演变情况尚不清楚。我们比较了根据神经肿瘤免疫治疗反应评估(iRANO)和标准神经肿瘤反应评估(RANO)影像学标准评估的GBM患者在ICB治疗期间的反应。
确定了在单一机构接受ICB治疗的49例GBM患者(7例新诊断患者和42例复发患者)。在ICB治疗期间,根据RANO标准对系列磁共振扫描上的肿瘤负荷进行定量。比较了iRANO和RANO的影像学反应评估。
82%(40/49)的患者接受抗PD-1治疗,16%(8/49)的患者接受抗PD-L1治疗,2%(1/49)的患者接受抗PD-1和抗CTLA4治疗。肿瘤负荷变化和最佳总体反应范围为-100%至+557%(中位数:+48%)。12%(6/49)的患者被RANO和iRANO均分类为一致的非进展者(最佳反应:1例完全缓解,1例部分缓解,4例疾病稳定)。另有12%(6/49)的患者评估结果不一致:RANO分级为疾病进展(PD)的患者中有15%(6/41)被iRANO分级为未确认的疾病进展(PDU)。这些评估结果不一致的患者的最终分类为:6例中有3例为假性进展(PsP),6例中有2例为PD,6例中有1例在iRANO对PDU进行评估之前退出研究,分类为PDU。在2例PD患者中,iRANO将PD诊断延迟了42天和93天。76%(37/49)的患者被RANO和iRANO均分类为一致的PD。所有患者中有12%(6/49)被分类为PsP,在ICB开始后中位12周(范围4 - 30周)开始出现。
标准RANO和iRANO在评估ICB开始6个月内患者的PD方面具有高度一致性。iRANO在6%(3/49)后来被证明为PsP的病例中有益,但在4%(2/49)的病例中将PD的确认延迟了不到3个月。12%的患者出现PsP,在ICB开始后长达7个月开始出现。需要进一步研究以确定在ICB治疗的GBM患者中,与iRANO相比,改良RANO的效用。