Predictive value of <sup>18</sup>F-FDG PET/CT in adults with T-cell lymphoblastic lymphoma: post hoc analysis of results from the GRAALL-LYSA LLO3 trial.

Becker, Stéphanie; Vermeulin, Thomas; Cottereau, Anne-Ségolène; Boissel, Nicolas; Vera, Pierre; Lepretre, Stéphane · Eur J Nucl Med Mol Imaging · 2017

retrospective_cohort · Level III

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Abstract

We examined whether FDG PET can be used to predict outcome in patients with lymphoblastic lymphoma (LL). This was a retrospective post hoc analysis of data from the GRAAL-LYSA LL03 trial, in which the treatment of LL using an adapted paediatric-like acute lymphoblastic leukaemia protocol was evaluated. PET data acquired at baseline and after induction were analysed. Maximum standardized uptake values (SUV<sub>max</sub>), total metabolic tumour volume and total lesion glycolysis were measured at baseline. The relative changes in SUV<sub>max</sub> from baseline (ΔSUV<sub>max</sub>) and the Deauville score were determined after induction. The population analysed comprised 36 patients with T-type LL. SUV<sub>max</sub> using a cut-off value of ≤8.76 vs. >8.76 was predictive of 3-year event-free survival (31.6% vs. 80.4%; p = 0.013) and overall survival (35.0% vs. 83.7%; p = 0.028). ΔSUV<sub>max</sub> using a cut-off value of ≤80% vs. >80% tended also to be predictive of 3-year event-free survival (40.0% vs. 76.0%; p = 0.054) and overall survival (49.2% vs. 85.6%; p = 0.085). Total metabolic tumour volume, baseline total lesion glycolysis and response according to the Deauville score were not predictive of outcome. A low initial SUV<sub>max</sub> was predictive of worse outcomes in our series of patients with T-type LL. Although relatively few patients were included, the study also suggested that ΔSUV<sub>max</sub> may be useful for predicting therapeutic efficacy.

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