TY - JOUR
T1 - PML risk is the main factor driving the choice of discontinuing natalizumab in a large multiple sclerosis population
T2 - results from an Italian multicenter retrospective study
AU - the Italian MS Register Study Group.
AU - Chisari, Clara G.
AU - Comi, Giancarlo
AU - Filippi, Massimo
AU - Paolicelli, Damiano
AU - Iaffaldano, Pietro
AU - Zaffaroni, Mauro
AU - Brescia Morra, Vincenzo
AU - Cocco, Eleonora
AU - Marfia, Girolama Alessandra
AU - Grimaldi, Luigi Maria
AU - Inglese, Matilde
AU - Bonavita, Simona
AU - Lugaresi, Alessandra
AU - Salemi, Giuseppe
AU - De Luca, Giovanna
AU - Cottone, Salvatore
AU - Conte, Antonella
AU - Sola, Patrizia
AU - Aguglia, Umberto
AU - Maniscalco, Giorgia Teresa
AU - Gasperini, Claudio
AU - Ferrò, Maria Teresa
AU - Pesci, Ilaria
AU - Amato, Maria Pia
AU - Rovaris, Marco
AU - Solaro, Claudio
AU - Lus, Giacomo
AU - Maimone, Davide
AU - Bergamaschi, Roberto
AU - Granella, Franco
AU - Di Sapio, Alessia
AU - Bertolotto, Antonio
AU - Totaro, Rocco
AU - Vianello, Marika
AU - Cavalla, Paola
AU - Bellantonio, Paolo
AU - Lepore, Vito
AU - Patti, Francesco
AU - Avolio, Carlo
AU - Balgera, Roberto
AU - Banfi, Paola
AU - Bramanti, Placido
AU - Capone, Lorenzo
AU - Cavalletti, Guido
AU - Chiveri, Luca
AU - Clerici, Raffaella
AU - Clerico, Marinella
AU - Corea, Francesco
AU - Dattola, Vincenzo
AU - De Robertis, Francesca
N1 - Funding Information:
Clara Grazia Chisari has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Giancarlo Comi has served as a Biogen, Merck, Mylan, Novartis, Roche, Sanofi/Genzyme and Teva Advisory Board Member. He received congress and travel/accommodation expense compensations or speaker honoraria from Biogen, Merck, Mylan, Novartis, Sanofi/Genzyme, Teva and Fondazione Italiana Sclerosi Multipla (FISM). Massimo Filippi is Editor-in-Chief of the Journal of Neurology; received compensation for consulting services and/or speaking activities from Biogen Idec, Merck-Serono, Novartis, Teva Pharmaceutical Industries; and receives research support from Biogen Idec, Merck-Serono, Novartis, Teva Pharmaceutical Industries, Roche, Italian Ministry of Health, Fondazione Italiana Sclerosi Multipla, and ARiSLA (Fondazione Italiana di Ricerca per la SLA). Damiano Paolicelli has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Pietro Iaffaldano has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Mauro Zaffaroni has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Vincenzo Brescia Morra: has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Eleonora Cocco has no conflict of interest. Girolama Alessandra Marfia: has served as an advisory board member and received speaker honoraria, congress, travel and accommodation expense compensations from Merck, Teva, Mylan, Bayer, Novartis, Roche, Almirall, Biogen and Sanofi Genzyme. Luigi Maria Grimaldi: has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Matilde Inglese: received honoraria or consultation fees from Roche, Biogen, Merck-Serono, Novartis, Genzyme and research grants from NIH, NMSS, FISM, and Teva Neuroscience. Simona Bonavita: Speaker and/or advisory board fee, and7or travel grant from Novartis, Teva, Sanofi-Genzyme, Roche, Biogen-Idec, Merck-Serono. Alessandra Lugaresi has served as a Biogen, Merck, Mylan, Novartis, Roche, Sanofi/ Genzyme and Teva Advisory Board Member. She received congress and travel/accommodation expense compensations or speaker honoraria from Biogen, Merck, Mylan, Novartis, Sanofi/Genzyme, Teva and Fondazione Italiana Sclerosi Multipla (FISM). Her institutions received research grants from Novartis. Paola Cavalla has served as an advisory board member for Almirall, Biogen, Merck-Serono, Sanofi-Genzyme, Roche, Teva; she has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Giuseppe Salemi: has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Giovanna De Luca has no conflict of interest. Salvatore Cottone: has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Antonella Conte: declares no conflict of interest. Patrizia Sola declares no conflict of interest. Umberto Aguglia has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Giorgia Teresa Maniscalco has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Claudio Gasperini declares no conflict of interest. Maria Teresa Ferrò: has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Ilaria Pesci declares no conflict of interest. Maria Pia Amato has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Marco Rovaris: received travel grants and fees for consulting and public speaking from Almirall, Biogen, Genzyme-Sanofi, Merck Serono, Mylan and Novartis. Claudio Solaro has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Giacomo Lus declares no conflict of interest. Davide Maimone declares no conflict of interest. Roberto Bergamaschi: declares no conflict of interest. Franco Granella has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Alessia Di Sapio received personal compensation for speaking and consulting by Biogen and Novartis and has been reimbursed by Merck, Biogen, Genzyme and Roche for attending several conferences. Antonio Bertolotto has received grants to attend scientific congresses or speaker honoraria from Biogen, Merck-Serono, Novartis, Roche, Sanofi/Genzyme, Teva. Rocco Totaro: declares no conflict of interest. Marika Vianello declares no conflict of interest. Paolo Bellantonio declares no conflict of interest. Vito Lepore declares no conflict of interest. Francesco Patti has received honoraria for speaking activities by Almirall, Bayer Schering, Biogen Idec, Merck Serono, Novartis, Roche, Sanofi Genzyme, and TEVA; he also served as advisory board member the following companies: Bayer Schering, Biogen Idec, Merck Serono, Novartis, Roche, Sanofi Genzyme, and TEVA; he was also funded by Pfizer and FISM for epidemiological studies; he received grants for congress participation from Almirall, Bayer Schering, Biogen Idec, Merck Serono, Novartis, Roche, Sanofi Genzyme, and TEVA.
Publisher Copyright:
© 2021, Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/2
Y1 - 2022/2
N2 - Background: Natalizumab (NTZ) is an effective treatment for relapsing–remitting multiple sclerosis (RRMS). However, patients and physicians may consider discontinuing NTZ therapy due to safety or efficacy issues. The aim of our study was to evaluate the NTZ discontinuation rate and reasons of discontinuation in a large Italian population of RRMS patients. Materials and methods: The data were extracted from the Italian MS registry in May 2018 and were collected from 51,845 patients in 69 Italian multiple sclerosis centers. MS patients with at least one NTZ infusion in the period between June 1st 2012 to May 15th 2018 were included. Discontinuation rates at each time point were calculated. Reasons for NTZ discontinuation were classified as “lack of efficacy”, “progressive multifocal leukoencephalopathy (PML) risk” or “other”. Results: Out of 51,845, 5151 patients, 3019 (58.6%) females, with a mean age of 43.6 ± 10.1 years (median 40), were analyzed. Out of 2037 (39.5%) who discontinued NTZ, a significantly higher percentage suspended NTZ because of PML risk compared to lack of efficacy [1682 (32.7% of 5151) vs 221 (4.3%), p < 0.001]; other reasons were identified for 99 (1.9%) patients. Patients discontinuing treatment were older, had longer disease duration and worse EDSS at the time of NTZ initiation and at last follow-up on NTZ treatment. The JCV index and EDSS at baseline were predictors for stopping therapy (HR 2.94, 95% CI 1.22–4.75; p = 0.02; HR 1.36, 95% CI 1.18–5.41; p = 0.04). Conclusions: Roughly 60% of MS patients stayed on NTZ treatment during the observation period. For those patients in whom NTZ discontinuation was required, it was mainly due to PML concerns.
AB - Background: Natalizumab (NTZ) is an effective treatment for relapsing–remitting multiple sclerosis (RRMS). However, patients and physicians may consider discontinuing NTZ therapy due to safety or efficacy issues. The aim of our study was to evaluate the NTZ discontinuation rate and reasons of discontinuation in a large Italian population of RRMS patients. Materials and methods: The data were extracted from the Italian MS registry in May 2018 and were collected from 51,845 patients in 69 Italian multiple sclerosis centers. MS patients with at least one NTZ infusion in the period between June 1st 2012 to May 15th 2018 were included. Discontinuation rates at each time point were calculated. Reasons for NTZ discontinuation were classified as “lack of efficacy”, “progressive multifocal leukoencephalopathy (PML) risk” or “other”. Results: Out of 51,845, 5151 patients, 3019 (58.6%) females, with a mean age of 43.6 ± 10.1 years (median 40), were analyzed. Out of 2037 (39.5%) who discontinued NTZ, a significantly higher percentage suspended NTZ because of PML risk compared to lack of efficacy [1682 (32.7% of 5151) vs 221 (4.3%), p < 0.001]; other reasons were identified for 99 (1.9%) patients. Patients discontinuing treatment were older, had longer disease duration and worse EDSS at the time of NTZ initiation and at last follow-up on NTZ treatment. The JCV index and EDSS at baseline were predictors for stopping therapy (HR 2.94, 95% CI 1.22–4.75; p = 0.02; HR 1.36, 95% CI 1.18–5.41; p = 0.04). Conclusions: Roughly 60% of MS patients stayed on NTZ treatment during the observation period. For those patients in whom NTZ discontinuation was required, it was mainly due to PML concerns.
KW - Discontinuation rate
KW - Multiple sclerosis
KW - Natalizumab
KW - Reasons for discontinuation
UR - http://www.scopus.com/inward/record.url?scp=85114169091&partnerID=8YFLogxK
U2 - 10.1007/s00415-021-10676-6
DO - 10.1007/s00415-021-10676-6
M3 - Article
C2 - 34181077
AN - SCOPUS:85114169091
SN - 0340-5354
VL - 269
SP - 933
EP - 944
JO - Journal of Neurology
JF - Journal of Neurology
IS - 2
ER -