Gregory Timothy A, Knight Stephanie R, Aaroe Ashley E, Highsmith Kaitlin N, Janatpour Zachary C, O'Brien Barbara J, Majd Nazanin K, Loghin Monica E, Patel Chirag B, Weathers Shiao-Pei, Puduvalli Vinay K, Kamiya-Matsuoka Carlos
Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Neurology, Madigan Army Medical Center, Tacoma, Washington, USA.
Neurooncol Pract. 2024 Apr 8;11(4):475-483. doi: 10.1093/nop/npae029. eCollection 2024 Aug.
We observed rapid tumor progression following COVID-19 infection among patients with glioblastoma and sought to systematically characterize their disease course in a retrospective case-control study.
Using an institutional database, we retrospectively identified a series of COVID-19-positive glioblastoma cases and matched them by age and sex 1:2 to glioblastoma controls who had a negative COVID-19 test during their disease course. Demographic and clinical data were analyzed. Hyperprogression was defined using modified response evaluation criteria in solid tumors criteria. Time to progression and overall survival were estimated using the Kaplan-Meier method.
Thirty-two glioblastoma cases with positive COVID-19 testing were matched to 64 glioblastoma controls with negative testing; age, sex, and molecular profiles did not differ between groups. Progression events occurred in 27 cases (84%) and 46 controls (72%). Of these, 14 cases (52%) presented with multifocal disease or leptomeningeal disease at progression compared with 10 controls (22%; = .0082). Hyperprogression was identified in 13 cases (48%) but only 4 controls (9%; = .0001). Cases had disease progression at a median of 35 days following COVID-19 testing, compared with 164 days for controls ( = .0001). Median survival from COVID-19 testing until death was 8.3 months for cases but 17 months for controls ( = .0016). Median overall survival from glioblastoma diagnosis was 20.7 months for cases and 24.6 months for controls ( = .672).
Patients with glioblastoma may have accelerated disease progression in the first 2 months after COVID-19 infection. Infected patients should be monitored vigilantly. Future investigations should explore tumor-immune microenvironment changes linking tumor progression and COVID-19.
我们观察到胶质母细胞瘤患者在感染新型冠状病毒肺炎(COVID-19)后肿瘤进展迅速,并试图在一项回顾性病例对照研究中系统地描述其病程。
利用机构数据库,我们回顾性地确定了一系列COVID-19阳性的胶质母细胞瘤病例,并按年龄和性别1:2与在病程中COVID-19检测呈阴性的胶质母细胞瘤对照进行匹配。分析了人口统计学和临床数据。采用实体瘤改良反应评估标准定义超进展。采用Kaplan-Meier法估计进展时间和总生存期。
32例COVID-19检测呈阳性的胶质母细胞瘤病例与64例检测呈阴性的胶质母细胞瘤对照相匹配;两组之间的年龄、性别和分子特征无差异。27例(84%)病例和46例对照(72%)发生进展事件。其中,14例(52%)在进展时出现多灶性疾病或软脑膜疾病,而对照为10例(22%;P = 0.0082)。13例(48%)病例被确定为超进展,而对照仅4例(9%;P = 0.0001)。病例在COVID-19检测后中位35天出现疾病进展,而对照为164天(P = 0.0001)。从COVID-19检测到死亡的中位生存期,病例为8.3个月,对照为17个月(P = 0.0016)。从胶质母细胞瘤诊断开始的中位总生存期,病例为20.7个月,对照为24.6个月(P = 0.672)。
胶质母细胞瘤患者在感染COVID-19后的前2个月可能疾病进展加速。应对感染患者进行密切监测。未来的研究应探索将肿瘤进展与COVID-19联系起来的肿瘤免疫微环境变化。