The role of positron emission tomography/computed tomography (PET/CT) in identifying Richter Syndrome (RS) is well established, while its impact on the survival of patients with chronic lymphocytic leukemia (CLL) has been less explored. The clinical characteristics and PET/CT data of 40 patients with a biopsy-proven CLL who required frontline chemoimmunotherapy, FCR (fludarabine, cyclophosphamide, rituximab) in 20 patients, BR (bendamustine, rituximab) in 20, were retrospectively analyzed. Standardized uptake volume (SUVmax) values ≥ 5 were observed more frequently in patients with deletion 11q (p = 0.006) and biopsies characterized by a rate of Ki67 positive cells ≥ 30% (p = 0.02). In the multivariate analysis, the presence of large and confluent PCs emerged as the only factor with a negative impact on progression-free survival (PFS), and overall survival (OS). Deletion 11q also revealed a significant and independent effect on PFS. SUVmax values ≥ 5 showed no statistical impact on PFS while in multivariate analysis, they revealed a significant adverse impact on OS (median survival probability not reached vs. 56 months; p = 0.002). Moreover, patients with higher SUVmax values more frequently developed Richter Syndrome (p = 0.015). Our results show that higher SUVmax values identify CLL patients with a pronounced rate of proliferating cells in the lymph-node compartment, inferior survival, and an increased risk of developing RS.

Prognostic significance of PET/CT in patients with chronic lymphocytic leukemia (CLL) treated with frontline chemoimmunotherapy / Porrazzo, M.; Nicolai, E.; Riminucci, M.; Vitale, C.; Coscia, M.; De Paoli, L.; Rago, A.; Buscicchio, G.; Maestrini, G.; Ligia, S.; Di Prima, A.; Corsi, A.; Caronna, R.; Gaidano, G.; Mauro, F. R.. - In: CANCERS. - ISSN 2072-6694. - 12:7(2020), pp. 1-11. [10.3390/cancers12071773]

Prognostic significance of PET/CT in patients with chronic lymphocytic leukemia (CLL) treated with frontline chemoimmunotherapy

Porrazzo M.;Nicolai E.;Riminucci M.;De Paoli L.;Rago A.;Maestrini G.;Ligia S.;Di Prima A.;Corsi A.;Caronna R.
Investigation
;
Mauro F. R.
2020

Abstract

The role of positron emission tomography/computed tomography (PET/CT) in identifying Richter Syndrome (RS) is well established, while its impact on the survival of patients with chronic lymphocytic leukemia (CLL) has been less explored. The clinical characteristics and PET/CT data of 40 patients with a biopsy-proven CLL who required frontline chemoimmunotherapy, FCR (fludarabine, cyclophosphamide, rituximab) in 20 patients, BR (bendamustine, rituximab) in 20, were retrospectively analyzed. Standardized uptake volume (SUVmax) values ≥ 5 were observed more frequently in patients with deletion 11q (p = 0.006) and biopsies characterized by a rate of Ki67 positive cells ≥ 30% (p = 0.02). In the multivariate analysis, the presence of large and confluent PCs emerged as the only factor with a negative impact on progression-free survival (PFS), and overall survival (OS). Deletion 11q also revealed a significant and independent effect on PFS. SUVmax values ≥ 5 showed no statistical impact on PFS while in multivariate analysis, they revealed a significant adverse impact on OS (median survival probability not reached vs. 56 months; p = 0.002). Moreover, patients with higher SUVmax values more frequently developed Richter Syndrome (p = 0.015). Our results show that higher SUVmax values identify CLL patients with a pronounced rate of proliferating cells in the lymph-node compartment, inferior survival, and an increased risk of developing RS.
2020
Chronic lymphocytic leukemia; PET/CT; Survival
01 Pubblicazione su rivista::01a Articolo in rivista
Prognostic significance of PET/CT in patients with chronic lymphocytic leukemia (CLL) treated with frontline chemoimmunotherapy / Porrazzo, M.; Nicolai, E.; Riminucci, M.; Vitale, C.; Coscia, M.; De Paoli, L.; Rago, A.; Buscicchio, G.; Maestrini, G.; Ligia, S.; Di Prima, A.; Corsi, A.; Caronna, R.; Gaidano, G.; Mauro, F. R.. - In: CANCERS. - ISSN 2072-6694. - 12:7(2020), pp. 1-11. [10.3390/cancers12071773]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1457579
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