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

Author:

Driessen Julia123ORCID,Zwezerijnen Gerben J. C.24ORCID,Schöder Heiko5ORCID,Kersten Marie José13ORCID,Moskowitz Alison J.6ORCID,Moskowitz Craig H.7ORCID,Eertink Jakoba J.28ORCID,Heymans Martijn W.9ORCID,Boellaard Ronald24ORCID,Zijlstra Josée M.28ORCID

Affiliation:

1. 1Department of Hematology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands

2. 2Division of Imaging and Biomarkers, Cancer Center Amsterdam, Amsterdam, The Netherlands

3. 3LYMMCARE, Lymphoma and Myeloma Center Amsterdam, Amsterdam, The Netherlands

4. 4Department of Radiology and Nuclear Medicine, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, The Netherlands

5. 5Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY

6. 6Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

7. 7Department of Medicine, Sylvester Comprehensive Cancer Center, Miami, FL

8. 8Department of Hematology, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands

9. 9Department of Epidemiology and Data Science, Amsterdam Public Health Research Institute, Amsterdam, The Netherlands

Abstract

Abstract 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 18F-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. These trials were registered at www.clinicaltrials.gov as #NCT02280993, #NCT00255723, and #NCT01508312.

Publisher

American Society of Hematology

Subject

Hematology

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