Ilkay Gulturk, Mesut Yilmaz, Seher Yildiz Tacar, Deniz Tural
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引用次数: 1
Abstract
Background: Nivolumab is a monoclonal antibody that binds to the programmed death-1 (PD-1) receptor and blocks its interaction with PD-L1 and PD-L2. High response rates have been achieved with its use in the treatment of metastatic renal cell carcinoma (mRCC). We aimed to determine a relationship between 18-Fluoro-2-Deoxy-D-Glucose Positron Emission Tomography/Computed Tomography (18F-FDG-PET/CT) performed before nivolumab treatment and treatment-related survival.
Methods: Between 2014 and 2021, 32 patients who received nivolumab and had pre-treatment 18F-FDG-PET/CT evaluation were included in this retrospective study. The total SUVmax (sum of SUVmax) of all tumoral foci and the lesion with the highest SUVmax value were recorded. The relationship of these values with progression-free survival (PFS) and overall survival (OS) was evaluated.
Results: The median highest SUVmax and sum of SUVmax values were found as 14.4 and 41.4, respectively. PFS and OS were longer in the group with a sum of SUVmax value below 41.4 compared to the group with a higher group (OS, median 9.52 vs. 4.2 months [P=0.018]; PFS, median 9.6 vs. 3 months [P=0.003], respectively). In the group with the highest SUVmax value below 14.4, PFS was evaluated as statistically significant compared to the higher group (PFS, median 16.74 vs. 3.3 months [P=0.004]), while OS was not found to be statistically significant (OS, median 25.45 vs. 16.74 months (P=0.110)).
Conclusions: Our study showed that there might be a relationship between SUVmax values and PFS and OS. The SUVmax values before nivolumab treatment can be used to predict prognosis and survival in mRCC patients.
背景:Nivolumab是一种与程序性死亡-1 (PD-1)受体结合并阻断其与PD-L1和PD-L2相互作用的单克隆抗体。在转移性肾细胞癌(mRCC)的治疗中取得了很高的反应率。我们的目的是确定在纳武单抗治疗前进行的18-氟-2-脱氧- d -葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG-PET/CT)与治疗相关生存率之间的关系。方法:2014年至2021年期间,32例接受纳武单抗治疗并进行治疗前18F-FDG-PET/CT评估的患者纳入本回顾性研究。记录所有肿瘤灶的总SUVmax (SUVmax之和)及SUVmax值最高的病变。评估这些值与无进展生存期(PFS)和总生存期(OS)的关系。结果:SUVmax最大值中位数为14.4,SUVmax值之和为41.4。SUVmax值总和低于41.4的组PFS和OS较SUVmax值较高的组更长(OS,中位9.52 vs. 4.2个月[P=0.018];PFS,中位9.6 vs. 3个月[P=0.003])。在SUVmax值低于14.4的最高组中,PFS与较高组相比具有统计学意义(PFS,中位数16.74 vs 3.3个月[P=0.004]),而OS无统计学意义(OS,中位数25.45 vs 16.74个月(P=0.110))。结论:我们的研究表明SUVmax值可能与PFS和OS有关。纳武单抗治疗前的SUVmax值可用于预测mRCC患者的预后和生存。