Development of a radiomics nomogram to predict the treatment resistance of Chinese MPO-AAV patients with lung involvement: a two-center study

被引:1
|
作者
Chen, Juan [1 ,2 ]
Meng, Ting [3 ]
Xu, Jia [3 ]
Ooi, Joshua D. D. [3 ,4 ]
Eggenhuizen, Peter J. J. [4 ]
Liu, Wenguang [1 ,2 ]
Li, Fang [1 ,2 ]
Wu, Xueqin [5 ]
Sun, Jian [5 ]
Zhang, Hao [5 ]
Zhou, Ya-Ou [6 ]
Luo, Hui [6 ]
Xiao, Xiangcheng [3 ]
Pei, Yigang [1 ,2 ]
Li, Wenzheng [1 ,2 ]
Zhong, Yong [3 ,7 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Radiol, Changsha, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Dept Nephrol, Changsha, Hunan, Peoples R China
[4] Monash Univ, Ctr Inflammatory Dis, Clayton, Vic, Australia
[5] Cent South Univ, Xiangya Hosp 3, Dept Nephrol, Changsha, Hunan, Peoples R China
[6] Cent South Univ, Xiangya Hosp, Dept Rheumatol & Immunol, Changsha, Peoples R China
[7] Cent South Univ, Xiangya Hosp, Key Lab Biol Nanotechnol Natl Hlth Commiss, Changsha, Hunan, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ANCA-associated vasculitis; myeloperoxidase; lung involvement; treatment resistance; radiomics nomogram; ANTIBODY-ASSOCIATED VASCULITIS; MICROSCOPIC POLYANGIITIS; RELAPSE; GRANULOMATOSIS; MANAGEMENT; DIAGNOSIS; CANCER;
D O I
10.3389/fimmu.2023.1084299
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BackgroundPrevious studies from our group and other investigators have shown that lung involvement is one of the independent predictors for treatment resistance in patients with myeloperoxidase (MPO)-anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (MPO-AAV). However, it is unclear which image features of lung involvement can predict the therapeutic response in MPO-AAV patients, which is vital in decision-making for these patients. Our aim was to develop and validate a radiomics nomogram to predict treatment resistance of Chinese MPO-AAV patients based on low-dose multiple slices computed tomography (MSCT) of the involved lung with cohorts from two centers. MethodsA total of 151 MPO-AAV patients with lung involvement (MPO-AAV-LI) from two centers were enrolled. Two different models (Model 1: radiomics signature; Model 2: radiomics nomogram) were built based on the clinical and MSCT data to predict the treatment resistance of MPO-AAV with lung involvement in training and test cohorts. The performance of the models was assessed using the area under the curve (AUC). The better model was further validated. A nomogram was constructed and evaluated by DCA and calibration curves, which further tested in all enrolled data and compared with the other model. ResultsModel 2 had a higher predicting ability than Model 1 both in training (AUC: 0.948 vs. 0.824; p = 0.039) and test cohorts (AUC: 0.913 vs. 0.898; p = 0.043). As a better model, Model 2 obtained an excellent predictive performance (AUC: 0.929; 95% CI: 0.827-1.000) in the validation cohort. The DCA curve demonstrated that Model 2 was clinically feasible. The calibration curves of Model 2 closely aligned with the true treatment resistance rate in the training (p = 0.28) and test sets (p = 0.70). In addition, the predictive performance of Model 2 (AUC: 0.929; 95% CI: 0.875-0.964) was superior to Model 1 (AUC: 0.862; 95% CI: 0.796-0.913) and serum creatinine (AUC: 0.867; 95% CI: 0.802-0.917) in all patients (all p< 0.05). ConclusionThe radiomics nomogram (Model 2) is a useful, non-invasive tool for predicting the treatment resistance of MPO-AAV patients with lung involvement, which might aid in individualizing treatment decisions.
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页数:13
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