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Pediatric Hodgkin Lymphoma

Cristina FerrariNuclear Medicine Unit, D.I.M. Department of Pediatric Hematology and Oncology, University of Bari "Aldo Moro", Bari, ItalyArtor Niccoli AsabellaNuclear Medicine Unit, D.I.MNunzio MerendaNuclear Medicine Unit, D.I.MCorinna AltiniNuclear Medicine Unit, D.I.MMargherita FanelliNuclear Medicine Unit, D.I.MPaola MuggeoDepartment of Pediatric Hematology and Oncology, University of Bari “Aldo Moro”, Bari, ItalyFrancesco De LeonardisDepartment of Pediatric Hematology and Oncology, University of Bari “Aldo Moro”, Bari, ItalyTeresa PerilloDepartment of Pediatric Hematology and Oncology, University of Bari “Aldo Moro”, Bari, ItalyNicola SantoroDepartment of Pediatric Hematology and Oncology, University of Bari “Aldo Moro”, Bari, ItalyGiuseppe RubiniNuclear Medicine Unit, D.I.M
Medicinejournal2017en
ABI

Аннотация

We investigated the prognostic value of interim F-FDG PET/CT (PET-2) in pediatric Hodgkin lymphoma (pHL), evaluating both visual and semiquantitative analysis.Thirty pHL patients (age ≤16) underwent serial F-FDG PET/CT: at baseline (PET-0), after 2 cycles of chemotherapy (PET-2) and at the end of first-line chemotherapy (PET-T). PET response assessment was carried out visually according to the Deauville Score (DS), as well as semiquantitatively by using the semiquantitative parameters reduction from PET-0 to PET-2 (ΔΣSUVmax0-2, ΔΣSUVmean0-2). Final clinical response assessment (outcome) at the end of first-line chemotherapy was the criterion standard, considering patients as responders (R) or nonresponders (NR). Disease status was followed identifying patients with absence or relapsed/progression disease (mean follow-up: 24 months, range 3-78).Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy of visual and semiquantitative assessment were calculated; furthermore, Fisher exact test was performed to evaluate the association between both visual and semiquantitative assessment and outcome at the end of the first-line chemotherapy. The prognostic capability of PET-2 semiquantitative parameters was calculated by ROC analysis and expressed as area under curve (AUC). Finally, progression-free survival (PFS) was analyzed according to PET-2 results based on the 5-point scale and semiquantitative criteria, using the Kaplan-Meier method.Based on the outcome at the end of first-line chemotherapy, 5 of 30 patients were NR, the remnant 25 of 30 were R. Sensitivity, specificity, PPV, NPV, and accuracy of visual analysis were 60%,72%,30%,90%,70%; conversely, sensitivity, specificity, PPV, NPV, and accuracy of semiquantitative assessment were 80%, 92%, 66.7%, 95.8%, 90%. The highest AUC resulted for ΔΣSUVmax0-2 (0.836; cut-off <12.5; sensitivity 80%; specificity 91%). The association between ΔΣSUVmax0-2 and outcome at the end of first-line chemotherapy resulted to have a strong statistical significance (P = 0.0026). Both methods demonstrated to influence PFS, even if the semiquantitative assessment allowed a more accurate identification of patients with a high risk of treatment failure (P = 0.005).Our preliminary results showed that PET-2 visual assessment, by using Deauville criteria, can be improved by using the semiquantitative analysis. The SUV max reduction (ΔΣSUVmax0-2) evaluation might provide a support for the interpretation of intermediate scores, predicting with good confidence those patients who will have a poor outcome and require alternative therapies.

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