Açikgoz Yusuf, Gurler Fatih, Inci Bediz Kurt, Ergun Yakup, Ucar Gokhan, Dirikoc Merve, Esen Selin Akturk, Tekin Berna Okudan, Bal Oznur, Dogan Mutlu, Uncu Dogan
Department of Medical Oncology, Health Science University, Ankara City Hospital.
Department of Medical Oncology, Gazi University Medicine Faculty.
Medicine (Baltimore). 2020 Nov 25;99(48):e23168. doi: 10.1097/MD.0000000000023168.
Stage III non-small cell lung cancer (NSCLC) is a highly heterogeneous subtype of lung cancer. There are still no widely accepted prognostic parameters for stage III NSCLC. In this study, we evaluated the prognostic value of the standardized uptake value (SUV) max ratio of primary tumor to lymph node (T/N SUV max) and its correlation with various hematological parameters.Patient data were reviewed from the hospital database retrospectively. The T/N SUV max ratio was calculated by dividing the SUV max of the primary tumor by the maximal SUV max of the lymph node. The cut-off value for T/N SUV max ratio was determined by receiver operating characteristic analysis. Survival analysis was performed by Kaplan-Meier method with the Long-rank test. P value < .05 was considered statistically significant.A total of 52 patients were included in this study. The optimal cut-off value for T/N SUV max was 1.96 (area under the curve: 0.74; 72.7% sensitivity and 73.7% specificity). Patients with T/N SUV max ≤1.96 were defined as high risk patients and those with >1.96 were defined as low risk patients. The median event (recurrence or progression) free survival was 24.3 months (95% confidence interval: 12.0-36.6) for low risk patients, and 9.2 months (95% confidence interval: 6.1-12.4) for high risk patients (P = .0015). There was an inverse correlation between T/N SUV max and hemoglobin concentration and mean corpuscular volume (rho: -0.349, P = .011; rho: -0.312, P = .025, respectively).Low risk patients had a more favorable prognosis compared to high risk patients. We demonstrated that T/N SUV max can be of prognostic value in stage III NSCLC. T/N SUV max correlated only with hemoglobin and mean corpuscular volume.
III期非小细胞肺癌(NSCLC)是肺癌的一种高度异质性亚型。目前仍没有被广泛接受的III期NSCLC预后参数。在本研究中,我们评估了原发肿瘤与淋巴结标准化摄取值(SUV)最大值之比(T/N SUV max)的预后价值及其与各种血液学参数的相关性。
我们回顾性地查阅了医院数据库中的患者数据。T/N SUV max比值通过将原发肿瘤的SUV max除以淋巴结的最大SUV max来计算。T/N SUV max比值的临界值通过受试者工作特征分析来确定。生存分析采用Kaplan-Meier法和长秩检验。P值<0.05被认为具有统计学意义。
本研究共纳入52例患者。T/N SUV max的最佳临界值为1.96(曲线下面积:0.74;灵敏度72.7%,特异度73.7%)。T/N SUV max≤1.96的患者被定义为高危患者,而T/N SUV max>1.96的患者被定义为低危患者。低危患者的中位无事件(复发或进展)生存期为24.3个月(95%置信区间:12.0 - 36.6),高危患者为9.2个月(95%置信区间:6.1 - 12.4)(P = 0.0015)。T/N SUV max与血红蛋白浓度和平均红细胞体积呈负相关(相关系数分别为:-0.349,P = 0.011;-0.312,P = 0.025)。
与高危患者相比,低危患者的预后更有利。我们证明T/N SUV max在III期NSCLC中具有预后价值。T/N SUV max仅与血红蛋白和平均红细胞体积相关。