MAXIMUM STANDARDIZED UPTAKE VALUE FROM STAGING FDG-PET/CT DOES NOT PREDICT TREATMENT OUTCOME FOR EARLY-STAGE NON SMALL-CELL LUNG CANCER TREATED WITH STEREOTACTIC BODY RADIOTHERAPY

MAXIMUM STANDARDIZED UPTAKE VALUE FROM STAGING FDG-PET/CT DOES NOT PREDICT TREATMENT OUTCOME FOR EARLY-STAGE NON SMALL-CELL LUNG CANCER TREATED WITH STEREOTACTIC BODY RADIOTHERAPY
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DOI:
10.1016/j.ijrobp.2009.09.081
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发表时间:
2010-11-15
影响因子:
7
通讯作者:
Videtic, Gregory M. M.
Videtic, Gregory M. M.
中科院分区:
医学1区
文献类型:
--
作者:
Burdick, Michael J.;Stephans, Kevin L.;Videtic, Gregory M. M.

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目的:进行回顾性分析,以确定2-脱氧-2- [(18)F]氟-D-葡萄糖(FDG)正电子发射断层扫描/计算机断层扫描(PET/CT)研究分期的最大标准化摄取值(SUV(max))是否与立体定向体部放疗(SBRT)治疗的早期非小细胞肺癌(NSCLC)的结局相关。2003年10月17日至2007年8月17日期间,72名医学上无法手术的患者接受了SBRT治疗T1- 2N 0 M0 NSCLC。SBRT采用腹部压迫和图像引导SBRT,分3次给予60戈伊,分5次给予50戈伊,或分10次给予50戈伊。考克斯比例风险回归分析,以确定是否PET SUV(最大值)和其他变量的影响结果:纵隔失败(MF),远处转移(DM),和总生存期(OS)。49例患者患有T1 N 0疾病,23例患有T2 N 0疾病。中位SUV(max)为6.55(范围:1.5-21)。中位随访时间为16.9个月(范围:0.1-37.9个月)。有3例局部失败,8例MF,19例DM和30例死亡。2年局部控制率、ME、DM和OS率分别为94.0%、10.4%、30.1%和61.3%。在单变量分析中,PET/CT SUV(max),定义为连续或二分变量,不能预测MF、DM或OS。在多变量分析中,总生存率的唯一预测因素是T1分期(风险比= 0.331 [95%置信区间,0.156-0.701],p = 0.0039)和吸烟包-年史结论:在接受SBRT治疗的早期NSCLC患者中,治疗前PET SUV(max)不能预测MF、DM或OS。(C)2010年爱思唯尔公司
Purpose: To perform a retrospective review to determine whether maximum standardized uptake values (SUV(max)) from staging 2-deoxy-2- [(18)F] fluoro-D-glucose (FDG) positron emission tomography/computed tomography (PET/CT) studies are associated with outcomes for early-stage non small-cell lung cancer (NSCLC) treated with stereotactic body radiotherapy (SBRT).Methods and Materials: Seventy-two medically inoperable patients were treated between October 17, 2003 and August 17, 2007 with SBRT for T1-2N0M0 NSCLC. SBRT was administered as 60 Gy in 3 fractions, 50 Gy in 5 fractions, or 50 Gy in 10 fractions using abdominal compression and image-guided SBRT. Cox proportional hazards regression was performed to determine whether PET SUV(max) and other variables influenced outcomes: mediastinal failure (MF), distant metastases (DM), and overall survival (OS).Results: Biopsy was feasible in 49 patients (68.1%). Forty-nine patients had T1N0 disease, and 23 had T2N0 disease. Median SUV(max) was 6.55 (range, 1.5-21). Median follow-up was 16.9 months (range, 0.1-37.9 months). There were 3 local failures, 8 MF, 19 DM, and 30 deaths. Two-year local control, ME, DM, and OS rates were 94.0%, 10.4%, 30.1%, and 61.3%, respectively. In univariate analysis, PET/CT SUV(max), defined either as a continuous or dichotomous variable, did not predict for MF, DM, or OS. On multivariable analysis, the only predictors for overall survival were T1 stage (hazard ratio = 0.331 [95% confidence interval, 0.156-0.701],p = 0.0039) and smoking pack-year history (hazard ratio = 1.015 [95% confidence interval, 1.004-1.0261], p = 0.0084).Conclusions: Pretreatment PET SUV(max) did not predict for MF, DM, or OS in patients treated with SBRT for early-stage NSCLC. (C) 2010 Elsevier Inc.