We analyzed metabolic response using interim positron emission tomography scan (iPET) in a subset of patients with follicular lymphoma (FL) enrolled in the randomized FOLL12 trial. Patients with grade 1-3a FL with an iPET performed between cycles 4 and 5 of first-line immunochemotherapy (ICT) were included; PET scan had to be centrally reviewed for the definition of Deauville score (DS) and were considered positive for DS 4-5. Overall 123 patients out of 211 with iPET were available for central review. Of these, 43% were older than 60, 33% had high-risk FLIPI2, and 47% received rituximab-bendamustine as the induction regimen. iPET showed a complete metabolic response (CMR) in 83% of cases. CMR at the end-of-induction therapy PET scan (eoiPET) was confirmed in 91% of iPET-negative patients. The 5-year progression-free survival (PFS) was 70% for iPET-negative and 34% for iPET-positive cases. In multivariate analysis, positive iPET was an independent prognostic factor for PFS. Combining iPET and eoiPET, the 3-year PFS was 78% for both negative iPET and eoiPET, with a reduced risk of progression compared to double-positive iPET/eoiPET cases. The 5-year overall survival rate was 96% for iPET-negative and 85% for DS 4-5. Our results confirm that iPET in patients with FL treated with standard ICT is a strong prognostic factor. Assessment of early metabolic response in FL may be considered for defining a novel generation of early response-adapted trials in FL. This trial was registered at www.ClinicalTrials.gov as #NCT02063685.

Prognostic role of interim PET in follicular lymphoma: a post hoc study of FOLL12 trial by Fondazione Italiana Linfomi / Durmo, R; Chauvie, S; Fallanca, F; Bergesio, F; Pinto, A; Del Giudice, I; Coscia, M; Corradini, P; Angelucci, E; Tosi, P; Freilone, R; Ballerini, F; Bari, A; Pastore, D; Zinzani, Pl; Bolis, S; Flenghi, L; Liso, A; Olivieri, J; Marcheselli, L; Merli, M; Versari, A; Guerra, L; Luminari, S.. - In: BLOOD ADVANCES. - ISSN 2473-9537. - 12:9(2025), pp. 2927-2934. [10.1182/bloodadvances.2024014790]

Prognostic role of interim PET in follicular lymphoma: a post hoc study of FOLL12 trial by Fondazione Italiana Linfomi.

Del Giudice I;
2025

Abstract

We analyzed metabolic response using interim positron emission tomography scan (iPET) in a subset of patients with follicular lymphoma (FL) enrolled in the randomized FOLL12 trial. Patients with grade 1-3a FL with an iPET performed between cycles 4 and 5 of first-line immunochemotherapy (ICT) were included; PET scan had to be centrally reviewed for the definition of Deauville score (DS) and were considered positive for DS 4-5. Overall 123 patients out of 211 with iPET were available for central review. Of these, 43% were older than 60, 33% had high-risk FLIPI2, and 47% received rituximab-bendamustine as the induction regimen. iPET showed a complete metabolic response (CMR) in 83% of cases. CMR at the end-of-induction therapy PET scan (eoiPET) was confirmed in 91% of iPET-negative patients. The 5-year progression-free survival (PFS) was 70% for iPET-negative and 34% for iPET-positive cases. In multivariate analysis, positive iPET was an independent prognostic factor for PFS. Combining iPET and eoiPET, the 3-year PFS was 78% for both negative iPET and eoiPET, with a reduced risk of progression compared to double-positive iPET/eoiPET cases. The 5-year overall survival rate was 96% for iPET-negative and 85% for DS 4-5. Our results confirm that iPET in patients with FL treated with standard ICT is a strong prognostic factor. Assessment of early metabolic response in FL may be considered for defining a novel generation of early response-adapted trials in FL. This trial was registered at www.ClinicalTrials.gov as #NCT02063685.
2025
follicular lymphoma; PET/CT; FOLL12 trial
01 Pubblicazione su rivista::01a Articolo in rivista
Prognostic role of interim PET in follicular lymphoma: a post hoc study of FOLL12 trial by Fondazione Italiana Linfomi / Durmo, R; Chauvie, S; Fallanca, F; Bergesio, F; Pinto, A; Del Giudice, I; Coscia, M; Corradini, P; Angelucci, E; Tosi, P; Freilone, R; Ballerini, F; Bari, A; Pastore, D; Zinzani, Pl; Bolis, S; Flenghi, L; Liso, A; Olivieri, J; Marcheselli, L; Merli, M; Versari, A; Guerra, L; Luminari, S.. - In: BLOOD ADVANCES. - ISSN 2473-9537. - 12:9(2025), pp. 2927-2934. [10.1182/bloodadvances.2024014790]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1742153
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