Significant dose reduction employing dual-low-dose PET/CT in pediatric lymphoma: maintaining diagnostic, staging, and response-assessing efficacy
摘要
To evaluate the clinical efficacy of a dual-low-dose total-body PET/CT protocol in pediatric lymphoma patients, incorporating low-dose PET imaging in combination with two distinct low-dose CT acquisition strategies.
Materials and methodsPediatric lymphoma patients (≤ 18 years) receiving half-dose [18F]FDG (1.85 ± 0.2 MBq/kg) were prospectively enrolled and divided into low-dose CT group (LDCT) and ultra-low-dose CT group (ULDCT) using uEXPLORER scanner. Image quality was evaluated based on subjective and objective metrics. The reference standard of lesions was confirmed with pathological and follow-up evidence. The effective dose (ED), the diagnostic efficacy for detecting lesions, and the accuracy for staging, treatment responses were compared. Institutional Review Board approval was obtained.
ResultsA total of 246 pediatric patients were enrolled (9.2 ± 3.8 years, 180 male). The LDCT (n = 127) and ULDCT (n = 119) had similar clinical characteristics (p > 0.05) except for male percentage (78.7% vs. 67.2%, p = 0.042). The total ED of ULDCT was significantly lower than that of LDCT (5.6 ± 1.9 mSv vs. 9.7 ± 3.2 mSv, p < 0.001). Both groups showed acceptable subject image quality and were comparable in main objective parameters. ULDCT showed a sensitivity lower than LDCT (99.0% vs. 99.9%, p = 0.010) in diagnosing lymph node lesions, while their specificity (96.0% vs. 94.3%) and area under curve (AUC, 0.978 vs. 0.982) were similar (both p > 0.05). LDCT and ULDCT were also comparable in diagnosing extranodal involvements (AUCs > 0.800), staging accuracy (94.6% and 93.6%), and response assessment accuracy (97.6% and 96.3%).
ConclusionsDual-low-dose total-body PET/CT allowed a significant reduction in total ED without compromising imaging quality and diagnosis performance in pediatric lymphoma patients.
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