Prognostic model using 18F-FDG PET radiomics predicts progression-free survival in relapsed/refractory Hodgkin lymphoma

被引:5
|
作者
Driessen, Julia [1 ,2 ,3 ,10 ]
Zwezerijnen, Gerben J. C. [2 ,4 ]
Schoeder, Heiko [5 ]
Kersten, Marie Jose [1 ,3 ]
Moskowitz, Alison J. [6 ]
Moskowitz, Craig H. [7 ]
Eertink, Jakoba J. [2 ,3 ]
Heymans, Martijn W. [9 ]
Boellaard, Ronald [2 ,3 ]
Zijlstra, Josee M. [2 ,8 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Hematol, Amsterdam, Netherlands
[2] Canc Ctr Amsterdam, Div Imaging & Biomarkers, Amsterdam, Netherlands
[3] Lymphoma & Myeloma Ctr Amsterdam, LYMMCARE, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Amsterdam Univ, Med Ctr, Dept Radiol & Nucl Med, Amsterdam, Netherlands
[5] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY USA
[6] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
[7] Sylvester Comprehens Canc Ctr, Dept Med, Miami, FL USA
[8] Vrije Univ Amsterdam, Amsterdam Univ, Med Ctr, Dept Hematol, Amsterdam, Netherlands
[9] Amsterdam Publ Hlth Res Inst, Dept Epidemiol & Data Sci, Amsterdam, Netherlands
[10] Univ Amsterdam, Amsterdam UMC, Dept Hematol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
关键词
METABOLIC TUMOR VOLUME; STEM-CELL TRANSPLANTATION; OPEN-LABEL; TOMOGRAPHY; OUTCOMES; THERAPY; TRIAL;
D O I
10.1182/bloodadvances.2023010404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Investigating prognostic factors in patients with relapsed or primary refractory classical Hodgkin lymphoma (R/R cHL) is essential to optimize risk-adapted treatment strategies. We built a prognostic model using baseline quantitative F-18-fluorodeoxyglucose positron emission tomography (PET) radiomics features and clinical characteristics to predict the progression-free survival (PFS) among patients with R/R cHL treated with salvage chemotherapy followed by autologous stem cell transplantation. Metabolic tumor volume and several novel radiomics dissemination features, representing interlesional differences in distance, volume, and standard uptake value, were extracted from the baseline PET. Machine learning using backward selection and logistic regression were applied to develop and train the model on a total of 113 patients from 2 clinical trials. The model was validated on an independent external cohort of 69 patients. In addition, we validated 4 different PET segmentation methods to calculate radiomics features. We identified a subset of patients at high risk for progression with significant inferior 3-year PFS outcomes of 38.1% vs 88.4% for patients in the low-risk group in the training cohort (P < .001) and 38.5% vs 75.0% in the validation cohort (P = .015), respectively. The overall survival was also significantly better in the low-risk group (P = .022 and P < .001). We provide a formula to calculate a risk score for individual patients based on the model. In conclusion, we developed a prognostic model for PFS combining radiomics and clinical features in a large cohort of patients with R/R cHL. This model calculates a PET-based risk profile and can be applied to develop risk-stratified treatment strategies for patients with R/R cHL.
引用
收藏
页码:6732 / 6743
页数:12
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