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Diagnostic and Predictive Values of 18 F-FDG PET/CT Metabolic Parameters in EGFR -Mutated Advanced Lung Adenocarcinoma

机译:EGFR蓄育晚期肺腺癌18型F-FDG PET / CT代谢参数的诊断和预测值

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Purpose: The clinical implications of the metabolic parameters of 18F-fluorodeoxyglucose positron emission tomography-computed tomography (18F-FDG PET/CT) in epidermal growth factor receptor ( EGFR) -mutated lung cancer are not fully understood. The aim of this study was to evaluate the diagnostic and prognostic utility of the parameters in EGFR -mutated lung cancer patients. Patients and Methods: We retrospectively enrolled 134 patients with advanced lung adenocarcinoma (72 EGFR -negative and 62 EGFR- positive). We evaluated the correlation between EGFR mutational status and the maximum standardized uptake value (SUVmax), as well as the associations between treatment outcomes in EGFR -mutated patients and various metabolic parameters of primary tumors. For the best predictive parameters, we calculated the metabolic tumor volume (MTV) and total lesion glycolysis (TLG) using two SUV cutoffs: 1.5 (MTV1.5, TLG1.5) and 2.5 (MTV2.5, TLG2.5). Results: Mean SUVmax was lower for EGFR -mutated tumors compared with EGFR wild-type (6.11 vs 10.41, p 0.001) tumors. Low SUVmax was significantly associated with positive EGFR mutation (odds ratio = 1.74). Multivariate analysis for survival demonstrated that high MTV1.5, TLG1.5, MTV2.5, and TLG2.5 were independently associated with shorter progression-free survival (PFS) and overall survival (OS), and the highest hazard ratios were found in TLG1.5 (3.26 for PFS and 4.62 for OS). Conclusion: SUVmax may be predictive for EGFR mutational status, and MTV and TLG of primary tumors may be promising prognostic parameters; 18F-FDG PET/CT has potential utility for the risk stratification of EGFR -mutated patients treated with targeted therapy.
机译:目的:在表皮生长因子受体(EGFR) - 矫形肺癌中,18F-氟脱氧葡萄糖正电子计算断层扫描(18F-FDG PET / CT)的临床意义尚未完全理解。该研究的目的是评估EGFR型肺癌患者参数的诊断和预后效用。患者及方法:我们回顾性地注册了134名晚期肺腺癌患者(72 egfr-Negative和62个Egfr-阳性)。我们评估了EGFR突变状态与最大标准化摄取值(SUVMAX)之间的相关性,以及EGFR次审计患者的治疗结果与原发性肿瘤的各种代谢参数之间的关联。对于最佳的预测参数,我们计算了使用两个SUV截止值的代谢肿瘤体积(MTV)和总损伤糖酵解(TLG):1.5(MTV1.5,TLG1.5)和2.5(MTV2.5,TLG2.5)。结果:与EGFR野生型(6.11 VS 10.41,P <0.001)肿瘤相比,EGFR型肿瘤的平均SUVMAX较低。低Suvmax与阳性EGFR突变显着相关(差距= 1.74)。生存的多变量分析证明了高MTV1.5,TLG1.5,MTV2.5和TLG2.5与无进展的存活(PFS)和总存活(OS)独立相关,并且发现了最高的危险比TLG1.5(3.26用于PFS和4.62的OS)。结论:Suvmax可预测EGFR突变状态,MTV和TLG的原发性肿瘤可能是有前途的预后参数; 18F-FDG PET / CT具有潜在的效用,用于患有靶向治疗治疗的EGFR的患者的风险分层。

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