TY - JOUR
T1 - Central Nervous System Involvement in CLL: An International Retrospective Study by ERIC, the European Research Initiative on CLL
AU - Chatzikonstantinou, Thomas
AU - Mikhaleva, Mariia
AU - Brieghel, Christian
AU - Papangelou, Christina
AU - Minga, Evangelia
AU - Arrais-Rodrigues, Celso
AU - Dimou-Besikli, Sotiria
AU - Cerutti, Amalia
AU - Doubek, Michael
AU - Enggaard, Lisbeth
AU - Espinet, Blanca
AU - Ferrer-Lores, Blanca
AU - Garcia Vela, Jose Antonio
AU - Gentile, Massimo
AU - Gimeno Vazquez, Eva
AU - Gutwein, Odit
AU - Herishanu, Yair
AU - Jabłonowska-Babij, Paula
AU - Jaksic, Ozren
AU - Josefsson, Pär
AU - Kalicińska, Elżbieta
AU - Kislova, Maria
AU - Lista, Enrico
AU - Kotsianidis, Ioannis
AU - Marquet, Juan
AU - Martino, Enrica Antonia Antonia
AU - McAuley, Ciaran P
AU - Mela-Osorio, Maria J
AU - Moia, Riccardo
AU - Mosquera Rubal, Claudia
AU - Nikitin, Eugene A.
AU - Pavlovsky, Miguel Arturo
AU - Pfister, Verena
AU - Savaş, Emine Merve
AU - Scarfò, Lydia
AU - Sever, Matjaz
AU - Shvidel, Lev
AU - Simkovic, Martin
AU - Stavroyianni, Niki
AU - Talimtzi, Persefoni
AU - Tranidou, Antigoni
AU - Visentin, Andrea
AU - Vrachiolias, George
AU - Wasik-Szczepanek, Ewa
AU - Wróbel, Tomasz
AU - Yağcı, Münci
AU - Cellini, Alessandro
AU - Chatzidimitriou, Anastasia
AU - GAIDANO, Gianluca
AU - Anderson, Mary Ann
AU - Davids, Matthew S.
AU - Brown, Jennifer R.
AU - Niemann, Carsten Utoft
AU - Stamatopoulos, Kostas
AU - Ghia, Paolo
AU - Ahn, Inhye E.
AU - Koren-Michowitz, Maya
PY - 2025
Y1 - 2025
N2 - CNS involvement (CNSi) of chronic lymphocytic leukemia (CLL) is a rare condition with no consensus on diagnosis and limited evidence for management and outcome. Here we report an international, multicenter, retrospective study conducted by the European Research Initiative on CLL (ERIC). The study defined CNSi of CLL by: 1) detection of CLL cells in the cerebrospinal fluid or confirmation of CLL infiltration of the CNS based on a tissue biopsy, 2) clinical or radiographic evidence of neurologic disease, and 3) the absence of other explanations for the neurologic findings. A total of 48 patients from 26 centers in 15 countries met all three diagnostic criteria of CLL-CNSi. Median age at diagnosis of CNSi was 64 years. Most patients were males (73%), had Binet stage A at CLL diagnosis (61%), and had untreated CLL at the time of CNSi (63%). Motor impairment was the most common symptom (38%) followed by visual impairment (32%). Of 47 patients who received treatment for CNSi, half (51%) received targeted agents, most commonly a BTK inhibitor (BTKi), and 34% received chemoimmunotherapy (CIT). Initial treatment was highly effective, leading to a reduction (83%) or complete resolution (71%) of neurologic symptoms and imaging findings in most patients. The estimated 5-year overall survival (OS) from the CNSi diagnosis was 77.1%. 5-year time-to-next-treatment or death was 94% for patients treated with BTKis compared to 64% for those treated with CIT. Treatment-sensitive disease, represented by attainment of CNS complete response after initial therapy, was associated with longer OS.
AB - CNS involvement (CNSi) of chronic lymphocytic leukemia (CLL) is a rare condition with no consensus on diagnosis and limited evidence for management and outcome. Here we report an international, multicenter, retrospective study conducted by the European Research Initiative on CLL (ERIC). The study defined CNSi of CLL by: 1) detection of CLL cells in the cerebrospinal fluid or confirmation of CLL infiltration of the CNS based on a tissue biopsy, 2) clinical or radiographic evidence of neurologic disease, and 3) the absence of other explanations for the neurologic findings. A total of 48 patients from 26 centers in 15 countries met all three diagnostic criteria of CLL-CNSi. Median age at diagnosis of CNSi was 64 years. Most patients were males (73%), had Binet stage A at CLL diagnosis (61%), and had untreated CLL at the time of CNSi (63%). Motor impairment was the most common symptom (38%) followed by visual impairment (32%). Of 47 patients who received treatment for CNSi, half (51%) received targeted agents, most commonly a BTK inhibitor (BTKi), and 34% received chemoimmunotherapy (CIT). Initial treatment was highly effective, leading to a reduction (83%) or complete resolution (71%) of neurologic symptoms and imaging findings in most patients. The estimated 5-year overall survival (OS) from the CNSi diagnosis was 77.1%. 5-year time-to-next-treatment or death was 94% for patients treated with BTKis compared to 64% for those treated with CIT. Treatment-sensitive disease, represented by attainment of CNS complete response after initial therapy, was associated with longer OS.
UR - https://iris.uniupo.it/handle/11579/221677
U2 - 10.1182/bloodadvances.2025017755
DO - 10.1182/bloodadvances.2025017755
M3 - Article
SN - 2473-9529
JO - Blood advances
JF - Blood advances
ER -