TY - JOUR
T1 - New Algorithms Improving PML Risk Stratification in MS Patients Treated With Natalizumab
AU - Toboso, Inmaculada
AU - Tejeda-Velarde, Amalia
AU - Alvarez-Lafuente, Roberto
AU - Arroyo, Rafael
AU - Hegen, Harald
AU - Deisenhammer, Florian
AU - Sainz de la Maza, Susana
AU - Alvarez-Cermeño, José C.
AU - Izquierdo, Guillermo
AU - Paramo, Dolores
AU - Oliva, Pedro
AU - Casanova, Bonaventura
AU - Agüera-Morales, Eduardo
AU - Franciotta, Diego
AU - Gastaldi, Matteo
AU - Fernández, Oscar
AU - Urbaneja, Patricia
AU - Garcia-Dominguez, José M.
AU - Romero, Fernando
AU - Laroni, Alicia
AU - Uccelli, Antonio
AU - Perez-Sempere, Angel
AU - Saiz, Albert
AU - Blanco, Yolanda
AU - Galimberti, Daniela
AU - Scarpini, Elio
AU - Espejo, Carmen
AU - Montalban, Xavier
AU - Rasche, Ludwig
AU - Paul, Friedemann
AU - González, Inés
AU - Álvarez, Elena
AU - Ramo, Cristina
AU - Caminero, Ana B.
AU - Aladro, Yolanda
AU - Calles, Carmen
AU - Eguía, Pablo
AU - Belenguer-Benavides, Antonio
AU - Ramió-Torrentà, Lluis
AU - Quintana, Ester
AU - Martínez-Rodríguez, José E.
AU - Oterino, Agustín
AU - López de Silanes, Carlos
AU - Casanova, Luis I.
AU - Landete, Lamberto
AU - Frederiksen, Jette
AU - Bsteh, Gabriel
AU - Mulero, Patricia
AU - Comabella, Manuel
AU - Hernández, Miguel A.
AU - Espiño, Mercedes
AU - Prieto, José M.
AU - Pérez, Domingo
AU - Otano, María
AU - Padilla, Francisco
AU - García-Merino, Juan A.
AU - Navarro, Laura
AU - Muriel, Alfonso
AU - Frossard, Lucienne Costa
AU - Villar, Luisa M.
N1 - Publisher Copyright:
© Copyright © 2020 Toboso, Tejeda-Velarde, Alvarez-Lafuente, Arroyo, Hegen, Deisenhammer, Sainz de la Maza, Alvarez-Cermeño, Izquierdo, Paramo, Oliva, Casanova, Agüera-Morales, Franciotta, Gastaldi, Fernández, Urbaneja, Garcia-Dominguez, Romero, Laroni, Uccelli, Perez-Sempere, Saiz, Blanco, Galimberti, Scarpini, Espejo, Montalban, Rasche, Paul, González, Álvarez, Ramo, Caminero, Aladro, Calles, Eguía, Belenguer-Benavides, Ramió-Torrentà, Quintana, Martínez-Rodríguez, Oterino, López de Silanes, Casanova, Landete, Frederiksen, Bsteh, Mulero, Comabella, Hernández, Espiño, Prieto, Pérez, Otano, Padilla, García-Merino, Navarro, Muriel, Frossard and Villar.
PY - 2020/12/17
Y1 - 2020/12/17
N2 - Overview: We assessed the role of age and disease activity as new factors contributing to establish the risk of progressive multifocal leucoencephalopathy in multiple sclerosis patients treated with natalizumab in 36 University Hospitals in Europe. We performed the study in 1,307 multiple sclerosis patients (70.8% anti-John Cunninghan virus positive antibodies) treated with natalizumab for a median time of 3.28 years. Epidemiological, clinical, and laboratory variables were collected. Lipid-specific IgM oligoclonal band status was available in 277 patients. Factors associated with progressive multifocal leucoencephalopathy onset were explored by uni- and multivariate logistic regression. Results: Thirty-five patients developed progressive multifocal leucoencephalopathy. The multivariate analysis identified anti-John Cunninghan virus antibody indices and relapse rate as the best predictors for the onset of this serious opportunistic infection in the whole cohort. They allowed to stratify progressive multifocal leucoencephalopathy risk before natalizumab initiation in individual patients [area under the curve (AUC) = 0.85]. The risk ranged from <1/3,300 in patients with anti-John Cunninghan virus antibody indices <0.9 and relapse rate >0.5, to 1/50 in the opposite case. In patients with lipid-specific IgM oligoclonal bands assessment, age at natalizumab onset, anti-John Cunninghan virus antibody indices, and lipid-specific IgM oligoclonal band status predicted progressive multifocal leucoencephalopathy risk (AUC = 0.92). The absence of lipid-specific IgM oligoclonal bands was the best individual predictor (OR = 40.94). The individual risk ranged from <1/10,000 in patients younger than 45 years at natalizumab initiation, who showed anti John Cunningham virus antibody indices <0.9 and lipid-specific IgM oligoclonal bands to 1/33 in the opposite case. Conclusions: In a perspective of personalized medicine, disease activity, anti-lipid specific IgM oligoclonal bands, anti Jonh Cunninghan virus antibody levels, and age can help tailor natalizumab therapy in multiple sclerosis patients, as predictors of progressive multifocal leucoencephalopathy.
AB - Overview: We assessed the role of age and disease activity as new factors contributing to establish the risk of progressive multifocal leucoencephalopathy in multiple sclerosis patients treated with natalizumab in 36 University Hospitals in Europe. We performed the study in 1,307 multiple sclerosis patients (70.8% anti-John Cunninghan virus positive antibodies) treated with natalizumab for a median time of 3.28 years. Epidemiological, clinical, and laboratory variables were collected. Lipid-specific IgM oligoclonal band status was available in 277 patients. Factors associated with progressive multifocal leucoencephalopathy onset were explored by uni- and multivariate logistic regression. Results: Thirty-five patients developed progressive multifocal leucoencephalopathy. The multivariate analysis identified anti-John Cunninghan virus antibody indices and relapse rate as the best predictors for the onset of this serious opportunistic infection in the whole cohort. They allowed to stratify progressive multifocal leucoencephalopathy risk before natalizumab initiation in individual patients [area under the curve (AUC) = 0.85]. The risk ranged from <1/3,300 in patients with anti-John Cunninghan virus antibody indices <0.9 and relapse rate >0.5, to 1/50 in the opposite case. In patients with lipid-specific IgM oligoclonal bands assessment, age at natalizumab onset, anti-John Cunninghan virus antibody indices, and lipid-specific IgM oligoclonal band status predicted progressive multifocal leucoencephalopathy risk (AUC = 0.92). The absence of lipid-specific IgM oligoclonal bands was the best individual predictor (OR = 40.94). The individual risk ranged from <1/10,000 in patients younger than 45 years at natalizumab initiation, who showed anti John Cunningham virus antibody indices <0.9 and lipid-specific IgM oligoclonal bands to 1/33 in the opposite case. Conclusions: In a perspective of personalized medicine, disease activity, anti-lipid specific IgM oligoclonal bands, anti Jonh Cunninghan virus antibody levels, and age can help tailor natalizumab therapy in multiple sclerosis patients, as predictors of progressive multifocal leucoencephalopathy.
KW - biomarkers
KW - demyelinating diseases
KW - disease modifying treatments
KW - multiple sclerosis
KW - natalizumab
KW - progressive multifocal leucoencephalopathy
U2 - 10.3389/fneur.2020.579438
DO - 10.3389/fneur.2020.579438
M3 - Journal article
C2 - 33408681
AN - SCOPUS:85098937296
VL - 11
JO - Frontiers in Neurology
JF - Frontiers in Neurology
SN - 1664-2295
M1 - 579438
ER -