Li Yan, Sijtsema Nanna Maria, de Vette Suzanne Petronella Maria, Steenbakkers Roel Johannes Henricus Marinus, Zhang Fan, Noordzij Walter, Van den Bosch Lisa, Langendijk Johannes Albertus, van Dijk Lisanne Vania
Department of Radiation Oncology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Department of Radiation Oncology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands.
Radiother Oncol. 2023 Mar;180:109458. doi: 10.1016/j.radonc.2022.109458. Epub 2023 Jan 3.
Previously, PET image biomarkers (PET-IBMs) - the 90 percentile standardized uptake value (P90-SUV) and the Mean SUV (Mean-SUV) of the contralateral parotid gland (cPG) - were identified as predictors for late-xerostomia following head and neck cancer (HNC) radiotherapy. The aim of the current study was to assess in an independent validation cohort whether these pre-treatment PET-IBM can improve late-xerostomia prediction compared to the prediction with baseline xerostomia and mean cPG dose alone.
The prediction endpoint was patient-rated moderate-to-severe xerostomia at 12 months after radiotherapy. The PET-IBMs were extracted from pre-treatment F-FDG PET images. The performance of the model (base model) with baseline xerostomia and mean cPG dose alone and models with additionally P90-SUV or Mean-SUV were tested in the current independent validation cohort. Specifically, model discrimination (area under the curve: AUC) and calibration (calibration plot) were evaluated.
The current validation cohort consisted of 137 patients of which 40% developed moderate-to-severe xerostomia at 12 months. Both the PET-P90 model (AUC:PET-P90 = 0.71) and the PET-Mean model (AUC: PET-Mean = 0.70) performed well in the current validation cohort. Moreover, their performance were improved compared to the base model (AUC:base model= 0.68). The calibration plots showed a good fit of the prediction to the actual rates for all tested models.
PET-IBMs showed an improved prediction of late-xerostomia when added to the base model in this validation cohort. This contributed to the published hypothesis that PET-IBMs include individualized information and can serve as a pre-treatment risk factor for late-xerostomia.
此前,正电子发射断层显像(PET)图像生物标志物(PET-IBM)——对侧腮腺(cPG)的第90百分位数标准化摄取值(P90-SUV)和平均SUV(Mean-SUV)——被确定为头颈部癌(HNC)放疗后迟发性口干的预测指标。本研究的目的是在一个独立验证队列中评估,与仅使用基线口干和cPG平均剂量进行预测相比,这些治疗前PET-IBM能否改善迟发性口干的预测。
预测终点为放疗后12个月患者自评的中重度口干。PET-IBM从治疗前的氟代脱氧葡萄糖(¹⁸F-FDG)PET图像中提取。在当前独立验证队列中测试仅使用基线口干和cPG平均剂量的模型(基础模型)以及另外加入P90-SUV或Mean-SUV的模型的性能。具体而言,评估模型的辨别力(曲线下面积:AUC)和校准(校准图)。
当前验证队列由137例患者组成,其中40%在12个月时出现中重度口干。PET-P90模型(AUC:PET-P90 = 0.71)和PET-Mean模型(AUC:PET-Mean = 0.70)在当前验证队列中表现良好。此外,与基础模型(AUC:基础模型 = 0.68)相比,它们的性能有所提高。校准图显示所有测试模型的预测与实际发生率拟合良好。
在该验证队列中,将PET-IBM添加到基础模型中时,其对迟发性口干的预测有所改善。这支持了已发表的假说,即PET-IBM包含个体化信息,可作为迟发性口干的治疗前危险因素。