de Geus-Oei L F, van Laarhoven H W M, Visser E P, Hermsen R, van Hoorn B A, Kamm Y J L, Krabbe P F M, Corstens F H M, Punt C J A, Oyen W J G
Department of Nuclear Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Ann Oncol. 2008 Feb;19(2):348-52. doi: 10.1093/annonc/mdm470. Epub 2007 Oct 24.
The aim of this prospective study was to evaluate the value of F-18-fluorodeoxyglucose-positron emission tomography (FDG-PET) for early assessment of chemotherapy response in patients with advanced colorectal cancer.
Dynamic FDG-PET was carried out before and at 2 (n = 50) and 6 months (n = 19) after the start of treatment. Quantitative Patlak analysis [metabolic rate of glucose (MRGlu)] and a simplified method to measure glucose metabolism [standardized uptake value (SUV)] were evaluated. The predictive value of changes in glucose metabolism was assessed with Cox proportional regression analysis. Overall survival (OS) and progression-free survival (PFS) were calculated using Kaplan-Meier estimates.
There was an increase in the rates of death (P = 0.049 for DeltaMRGlu PET1-2; P = 0.017 for DeltaSUV PET1-2; P = 0.032 for DeltaMRGlu PET1-3; P = 0.048 for DeltaSUV PET1-3) and progression (P = 0.026 for DeltaMRGlu PET1-2; P = 0.035 for DeltaSUV PET1-2; P = 0.041 for DeltaMRGlu PET1-3; P = 0.081 for DeltaSUV PET1-3) associated with worse response as assessed by PET on Cox proportional regression analysis. The OS and PFS analysis showed a significant predictive value at broad ranges of DeltaMRGlu and DeltaSUV cut-off levels.
The degree of chemotherapy-induced changes in tumor glucose metabolism is highly predictive for patient outcome. The use of FDG-PET for therapy monitoring seems clinically feasible since simplified methods (SUV) are sufficiently reliable.
本前瞻性研究旨在评估F-18-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)在晚期结直肠癌患者化疗反应早期评估中的价值。
在治疗开始前、治疗开始后2个月(n = 50)和6个月(n = 19)进行动态FDG-PET检查。评估了定量Patlak分析[葡萄糖代谢率(MRGlu)]和一种测量葡萄糖代谢的简化方法[标准化摄取值(SUV)]。采用Cox比例回归分析评估葡萄糖代谢变化的预测价值。使用Kaplan-Meier估计法计算总生存期(OS)和无进展生存期(PFS)。
通过Cox比例回归分析评估,与较差反应相关的死亡(DeltaMRGlu PET1-2,P = 0.049;DeltaSUV PET1-2,P = 0.017;DeltaMRGlu PET1-3,P = 0.032;DeltaSUV PET1-3,P = 0.048)和进展(DeltaMRGlu PET1-2,P = 0.026;DeltaSUV PET1-2,P = 0.035;DeltaMRGlu PET1-3,P = 0.041;DeltaSUV PET1-3,P = 0.081)发生率有所增加。OS和PFS分析显示,在DeltaMRGlu和DeltaSUV广泛的截断水平范围内具有显著的预测价值。
化疗引起的肿瘤葡萄糖代谢变化程度对患者预后具有高度预测性。由于简化方法(SUV)足够可靠,使用FDG-PET进行治疗监测在临床上似乎是可行的。