Radiomics signature from [18F]FDG PET images for prognosis predication of primary gastrointestinal diffuse large B cell lymphoma

被引:14
|
作者
Jiang, Chong [1 ]
Huang, Xiangjun [2 ]
Li, Ang [2 ]
Teng, Yue [1 ]
Ding, Chongyang [3 ]
Chen, Jianxin [2 ]
Xu, Jingyan [4 ]
Zhou, Zhengyang [1 ]
机构
[1] Nanjing Univ, Dept Nucl Med, Nanjing Drum Tower Hosp, Affiliated Hosp,Med Sch, Nanjing 210000, Peoples R China
[2] Nanjing Univ Posts & Telecommun, Key Lab Broadband Wireless Commun & Sensor Networ, Minist Educ, Nanjing, Peoples R China
[3] Nanjing Med Univ, Jiangsu Prov Hosp, Dept Nucl Med, Affiliated Hosp 1, Nanjing, Peoples R China
[4] Nanjing Univ, Dept Hematol, Nanjing Drum Tower Hosp, Affiliated Hosp,Med Sch, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
关键词
FDG PET; CT; Primary gastrointestinal diffuse large B cell lymphoma; Prognosis; Radiomics; METABOLIC TUMOR VOLUME; NCCN-IPI; R-CHOP; RITUXIMAB;
D O I
10.1007/s00330-022-08668-9
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives To investigate the prognostic value of PET radiomics feature in the prognosis of patients with primary gastrointestinal diffuse large B cell lymphoma (PGI-DLBCL) treated with R-CHOP-like regimen. Methods A total of 140 PGI-DLBCL patients who underwent pre-therapy [F-18] FDG PET/CT were enrolled in this retrospective analysis. PET radiomics features obtained from patients in the training cohort were subjected to three machine learning methods and Pearson's correlation test for feature selection. Support vector machine (SVM) was used to build a radiomics signature classifier associated with progression-free survival (PFS) and overall survival (OS). A multivariate Cox proportional hazards regression model was established to predict survival outcomes. Results A total of 1421 PET radiomics features were extracted and reduced to 5 features to build a radiomics signature which was significantly associated with PFS and OS (p < 0.05). The combined model incorporating radiomics signatures, metabolic metrics, and clinical risk factors showed high C-indices in both the training (PFS: 0.825, OS: 0.834) and validation sets (PFS: 0.831, OS: 0.877). Decision curve analysis (DCA) demonstrated that the combined models achieved the most net benefit across a wider reasonable range of threshold probabilities for predicting PFS and OS. Conclusion The newly developed radiomics signatures obtained by the ensemble strategy were independent predictors of PFS and OS for PGI-DLBCL patients. Moreover, the combined model with clinical and metabolic factors was able to predict patient prognosis and may enable personalized treatment decision-making.
引用
收藏
页码:5730 / 5741
页数:12
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