Prognostic value of baseline and interim [ 18 F]FDG PET metabolic parameters in pediatric Hodgkin’s lymphoma

Mikhail Ya. Yadgarov, M. M. Dunaykin,G. I. Shestopalov, C. Kailash, E. D. Kireeva, N. V. Myakova, Yu. N. Likar

European Journal of Nuclear Medicine and Molecular Imaging(2024)

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Abstract
Background Hodgkin lymphoma (HL) in pediatric populations has a high survival rate but poses risks for long-term morbidities. Although [ 18 F]fluoro‑2‑deoxy‑2‑d‑glucose positron emission tomography ([ 18 F]FDG PET) scans offer potential for improved risk stratification, the definitive prognostic value of quantitative [ 18 F]FDG PET parameters remains unclear for pediatric HL. Methods A single-center, retrospective study included pediatric patients diagnosed with HL between 2016 and 2023 treated according to EuroNet-PHL-C1 and DAL/GPOH-HD protocols. Patients underwent baseline and interim PET/CT scans after two chemotherapy cycles. Event-free survival (EFS) was the primary endpoint, Deauville score was the secondary endpoint. Quantitative [ 18 F]FDG PET parameters included SUVmax, metabolic tumor volume (MTV) and total lesion glycolysis (TLG) that were evaluated using two segmentation methods (SUV 2.5, 41% SUVmax). Survival outcomes were assessed using Cox regression analysis. Results A total of 115 patients (50 males, median age 14.2 years) were studied, with a median follow-up period of 35 months. During this period, 16 cases (13.9%) of relapse or progression were noted. Baseline and interim MTV 2.5, MTV 41%, TLG 2.5, and TLG 41%, along with interim SUVmax, were significantly associated with worse EFS and correlated with post-treatment Deauville scores. In multivariable analysis, interim MTV 2.5 > 0 ml (adj. hazard ratio, HR: 3.89, p = 0.009) and interim TLG 41% ≥ 30 g (adj. HR: 7.98, p = 0.006) were independent risk factors for EFS. Conclusion Baseline and interim [ 18 F]FDG PET parameters can serve as significant prognostic indicators for EFS and treatment response in pediatric HL. These quantitative measures could enhance individualized, risk-adapted treatment strategies for children and adolescents with HL.
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Key words
Pediatric Hodgkin Lymphoma,[18F]FDG PET,Event-free survival,Metabolic tumor volume,Total lesion glycolysis,Segmentation
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