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Positron emission tomography-computed tomography on predicting the efficacy of targeted therapy for lung adenocarcinoma

机译:正电子发射断层扫描/计算机断层扫描预测肺腺癌靶向治疗的疗效

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摘要

Background: In this study, positron emission tomography-computed tomography (PET-CT) was used to monitor the maximal standard uptake value (SUVmax) in advanced lung adenocarcinoma patients with epithermal growth factor receptor (EGFR) mutation to prove its role in predicting the prognosis of targeted therapy. Methods: A total of 46 patients with advanced lung adenocarcinoma (IIIb-IV stage) were enrolled in the current study. They were positive for EGFR mutation. All patients received gefitinib (250mg per day, administered orally). PET-CT was conducted prior to (at baseline) and six months after gefitinib administration for the lesion size and SUVmax. The recommendations of the European Organization for Research and Treatment of Cancer criteria were chosen for PET assessment. Metabolic response (SUV decline -25%) was compared with morphologic response evaluated by CT scan and overall survival. Result: Compared to patients with △SUV% ≥ 25% (progressive metabolic disease), the survival time was significantly prolonged in △SUV% -25% (including complete metabolic response and progressive metabolic disease) (10.6/18.4, P = 0.000), but was not in -25% ≤ △SUV% 25% (stable metabolic disease) (10.6/10.7, P = 0.088). Patients who achieved △SUV% -25% after treatment were associated with a longer median survival, higher control rate, and better prognosis. There was a strong correlation between SUV changes (△SUV%) and CT size change (△lesion size%) (R2 = 0.891, P = 0.000). Conclusion: Changes in the SUV could be used to predict the prognosis of targeted therapy in advanced lung adenocarcinoma.
机译:背景:在这项研究中,正电子发射断层扫描计算机断层扫描(PET-CT)用于监测患有超热生长因子受体(EGFR)突变的晚期肺腺癌患者的最大标准摄取值(SUVmax),以证明其在预测肺动脉高压中的作用。靶向治疗的预后。方法:本研究共纳入46例晚期肺腺癌(IIIb-IV期)患者。他们为EGFR突变阳性。所有患者均接受吉非替尼(每天250mg,口服)。在进行吉非替尼治疗前(基线时)和术后六个月进行PET-CT检查,以了解病变大小和SUVmax。选择了欧洲癌症研究和治疗组织标准的建议进行PET评估。将代谢反应(SUV下降<-25%)与通过CT扫描和总体生存率评估的形态学反应进行比较。结果:与△SUV%≥25%(进行性代谢疾病)相比,存活率在△SUV%<-25%(包括完全代谢反应和进行性代谢疾病)中显着延长(10.6 / 18.4,P = 0.000) ),但不是-25%≤△SUV%<25%(稳定的代谢性疾病)(10.6 / 10.7,P = 0.088)。治疗后达到△SUV%<-25%的患者与更长的中位生存期,更高的控制率和更好的预后相关。 SUV变化(△SUV%)和CT尺寸变化(△病变尺寸%)之间有很强的相关性(R2 = 0.891,P = 0.000)。结论:SUV的改变可用于预测靶向治疗晚期肺腺癌的预后。

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