Yue Haizhen, Li Xiaofan, You Jing, Feng Pujie, Du Yi, Wang Ruoxi, Wu Hao, Cheng Jinsheng, Ding Kuke, Jing Bin
National Institute for Radiological Protection, Chinese Center for Disease Control and Prevention, Beijing, China.
Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Radiation Oncology, Peking University Cancer Hospital & Institute, Beijing, China.
Front Oncol. 2024 May 21;14:1365897. doi: 10.3389/fonc.2024.1365897. eCollection 2024.
Acute hematologic toxicity (HT) is a prevalent adverse tissue reaction observed in cervical cancer patients undergoing chemoradiotherapy (CRT), which may lead to various negative effects such as compromised therapeutic efficacy and prolonged treatment duration. Accurate prediction of HT occurrence prior to CRT remains challenging.
A discovery dataset comprising 478 continuous cervical cancer patients (140 HT patients) and a validation dataset consisting of 205 patients (52 HT patients) were retrospectively enrolled. Both datasets were categorized into the CRT group and radiotherapy (RT)-alone group based on the treatment regimen, i.e., whether chemotherapy was administered within the focused RT duration. Radiomics features were derived by contouring three regions of interest (ROIs)-bone marrow (BM), femoral head (FH), and clinical target volume (CTV)-on the treatment planning CT images before RT. A comprehensive model combining the radiomics features as well as the demographic, clinical, and dosimetric features was constructed to classify patients exhibiting acute HT symptoms in the CRT group, RT group, and combination group. Furthermore, the time-to-event analysis of the discriminative ROI was performed on all patients with acute HT to understand the HT temporal progression.
Among three ROIs, BM exhibited the best performance in classifying acute HT, which was verified across all patient groups in both discovery and validation datasets. Among different patient groups in the discovery dataset, acute HT was more precisely predicted in the CRT group [area under the curve (AUC) = 0.779, 95% CI: 0.657-0.874] than that in the RT-alone (AUC = 0.686, 95% CI: 0.529-0.817) or combination group (AUC = 0.748, 95% CI: 0.655-0.827). The predictive results in the validation dataset similarly coincided with those in the discovery dataset: CRT group (AUC = 0.802, 95% CI: 0.669-0.914), RT-alone group (AUC = 0.737, 95% CI: 0.612-0.862), and combination group (AUC = 0.793, 95% CI: 0.713-0.874). In addition, distinct feature sets were adopted for different patient groups. Moreover, the predicted HT risk of BM was also indicative of the HT temporal progression.
HT prediction in cervical patients is dependent on both the treatment regimen and ROI selection, and BM is closely related to the occurrence and progression of HT, especially for CRT patients.
急性血液学毒性(HT)是接受放化疗(CRT)的宫颈癌患者中常见的不良组织反应,可能导致各种负面影响,如治疗效果受损和治疗时间延长。在CRT之前准确预测HT的发生仍然具有挑战性。
回顾性纳入一个发现数据集,包括478例连续性宫颈癌患者(140例HT患者)和一个验证数据集,由205例患者组成(52例HT患者)。根据治疗方案,即是否在聚焦放疗期间进行化疗,将两个数据集分为CRT组和单纯放疗(RT)组。通过在放疗前的治疗计划CT图像上勾勒三个感兴趣区域(ROI)——骨髓(BM)、股骨头(FH)和临床靶区(CTV),提取放射组学特征。构建一个综合模型,结合放射组学特征以及人口统计学、临床和剂量学特征,对CRT组、RT组和联合组中出现急性HT症状的患者进行分类。此外,对所有急性HT患者进行鉴别性ROI的事件发生时间分析,以了解HT的时间进程。
在三个ROI中,BM在分类急性HT方面表现最佳,这在发现和验证数据集中的所有患者组中都得到了验证。在发现数据集中的不同患者组中,CRT组对急性HT的预测更准确[曲线下面积(AUC)=0.779,95%可信区间:0.657-0.874],优于单纯RT组(AUC=0.686,95%可信区间:0.529-0.817)或联合组(AUC=0.748,95%可信区间:0.655-0.827)。验证数据集中的预测结果与发现数据集中的结果相似:CRT组(AUC=0.802,95%可信区间:0.669-0.914)、单纯RT组(AUC=0.737,95%可信区间:0.612-0.862)和联合组(AUC=0.793,95%可信区间:0.713-0.874)。此外,不同患者组采用了不同的特征集。而且,BM预测的HT风险也表明了HT的时间进程。
宫颈癌患者的HT预测取决于治疗方案和ROI选择,BM与HT的发生和进展密切相关,尤其是对于CRT患者。