Salem Usama, Amini Behrang, Chuang Hubert H, Daw Najat C, Wei Wei, Haygood Tamara Miner, Madewell John E, Costelloe Colleen M
Department of Diagnostic Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX.
Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
J Cancer. 2017 Aug 25;8(15):2892-2898. doi: 10.7150/jca.20077. eCollection 2017.
: The existing literature of 18 F-FDG PET/CT in Ewing sarcoma investigates mixed populations of patients with both soft tissue and bone primary tumors. The aim of our study was to evaluate whether the maximum standardized uptake value (SUVmax) obtained with 18F-FDG PET/CT before and after induction chemotherapy can be used as an indicator of survival in patients with Ewing sarcoma originating exclusively in the skeleton. A retrospective database search from 2004-2011 identified 28 patients who underwent 18 F-FDG PET/CT before (SUV1, n= 28) and after (SUV2, n=23) induction chemotherapy. Mean follow up was 3.3 years and median follow up for survivors was 6.3 years (range: 2.6-9.8 years). Multivariate and univariate Cox proportional hazard model was used to assess for correlation of SUV1, SUV2, and the change in SUVmax with overall survival (OS) and progression-free survival (PFS). Mean SUVmax was 10.74 before (SUV1) and after 4.11 (SUV2) induction chemotherapy. High SUV1 (HR = 1.05, 95% CI: 1.0-1.1, P = 0.01) and SUV2 (HR =1.2, 95% CI: 1.0-1.4, P = 0.01) were associated with worse OS. A cut off point of 11.6 was identified for SUV1. SUV1 higher than 11.6 had significantly worse OS (HR = 5.71, 95% CI: 1.85 - 17.61, P = 0.003) and PFS (HR = 3.16, 95% CI: 1.13 - 8.79, P = 0.03, P < 0.05 is significant). 18F-FDG PET/CT can be used as a prognostic indicator for survival in primary Ewing sarcoma of bone.
关于18F-FDG PET/CT在尤因肉瘤中的现有文献研究的是软组织和骨原发性肿瘤患者的混合群体。我们研究的目的是评估诱导化疗前后通过18F-FDG PET/CT获得的最大标准化摄取值(SUVmax)是否可作为仅起源于骨骼的尤因肉瘤患者生存的指标。对2004年至2011年的回顾性数据库搜索确定了28例在诱导化疗前(SUV1,n = 28)和后(SUV2,n = 23)接受18F-FDG PET/CT检查的患者。平均随访时间为3.3年,幸存者的中位随访时间为6.3年(范围:2.6 - 9.8年)。采用多变量和单变量Cox比例风险模型评估SUV1、SUV2以及SUVmax的变化与总生存期(OS)和无进展生存期(PFS)的相关性。诱导化疗前平均SUVmax为10.74(SUV1),化疗后为4.11(SUV2)。高SUV1(HR = 1.05,95% CI:1.0 - 1.1,P = 0.01)和SUV2(HR = 1.2,95% CI:1.0 - 1.4,P = 0.01)与较差的OS相关。确定SUV1的截断点为11.6。高于11.6的SUV1的OS(HR = 5.71,95% CI:1.85 - 17.61,P = 0.003)和PFS(HR = 3.16,95% CI:1.13 - 8.79,P = 0.03,P < 0.05具有显著性)明显更差。18F-FDG PET/CT可作为骨原发性尤因肉瘤生存的预后指标。