Your browser doesn't support javascript.
loading
New Algorithms Improving PML Risk Stratification in MS Patients Treated With Natalizumab.
Toboso, Inmaculada; Tejeda-Velarde, Amalia; Alvarez-Lafuente, Roberto; Arroyo, Rafael; Hegen, Harald; Deisenhammer, Florian; Sainz de la Maza, Susana; Alvarez-Cermeño, José C; Izquierdo, Guillermo; Paramo, Dolores; Oliva, Pedro; Casanova, Bonaventura; Agüera-Morales, Eduardo; Franciotta, Diego; Gastaldi, Matteo; Fernández, Oscar; Urbaneja, Patricia; Garcia-Dominguez, José M; Romero, Fernando; Laroni, Alicia; Uccelli, Antonio; Perez-Sempere, Angel; Saiz, Albert; Blanco, Yolanda; Galimberti, Daniela; Scarpini, Elio; Espejo, Carmen; Montalban, Xavier; Rasche, Ludwig; Paul, Friedemann; González, Inés; Álvarez, Elena; Ramo, Cristina; Caminero, Ana B; Aladro, Yolanda; Calles, Carmen; Eguía, Pablo; Belenguer-Benavides, Antonio; Ramió-Torrentà, Lluis; Quintana, Ester; Martínez-Rodríguez, José E; Oterino, Agustín; López de Silanes, Carlos; Casanova, Luis I; Landete, Lamberto; Frederiksen, Jette; Bsteh, Gabriel; Mulero, Patricia; Comabella, Manuel; Hernández, Miguel A.
Afiliação
  • Toboso I; Immunology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Tejeda-Velarde A; Immunology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Alvarez-Lafuente R; Instituto de Investigación Sanitaria San Carlos (IDISSC), Hospital Clinico San Carlos, Madrid, Spain.
  • Arroyo R; Department of Neurology, Hospital Universitario Quiron Salud, Madrid, Spain.
  • Hegen H; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Deisenhammer F; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Sainz de la Maza S; Neurology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Alvarez-Cermeño JC; Neurology Department, Hospital Universitario Ramon y Cajal, Madrid, Spain.
  • Izquierdo G; Neurology Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Paramo D; Neurology Department, Hospital Universitario Virgen Macarena, Sevilla, Spain.
  • Oliva P; Neurology Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Casanova B; Neurology Department, Hospital Universitario la Fe, Valencia, Spain.
  • Agüera-Morales E; Neurology Department, Hospital Universitario Reina Sofia, Cordoba, Spain.
  • Franciotta D; Istituti di Recovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation, Pavia, Italy.
  • Gastaldi M; Istituti di Recovero e Cura a Carattere Scientifico (IRCCS) Mondino Foundation, Pavia, Italy.
  • Fernández O; Neurology Department, Hospital Regional Universitario, Malaga, Spain.
  • Urbaneja P; Neurology Department, Hospital Regional Universitario, Malaga, Spain.
  • Garcia-Dominguez JM; Neurology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Romero F; Neurology Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Laroni A; University of Genoa, Ospedale Policlinico San Martino, Genoa, Italy.
  • Uccelli A; University of Genoa, Ospedale Policlinico San Martino, Genoa, Italy.
  • Perez-Sempere A; Neurology Department, Hospital General Universitario de Alicante, Alicante, Spain.
  • Saiz A; Neurology Service, Hospital Clinic and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
  • Blanco Y; Neurology Service, Hospital Clinic and Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
  • Galimberti D; Centro Dino Ferrari, Fondazione Ca' Granda, Istituti di Recovero e Cura a Carattere Scientifico (IRCCS) Ospedale Policlinico, University of Milan, Milan, Italy.
  • Scarpini E; Centro Dino Ferrari, Fondazione Ca' Granda, Istituti di Recovero e Cura a Carattere Scientifico (IRCCS) Ospedale Policlinico, University of Milan, Milan, Italy.
  • Espejo C; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Institut de Recerca, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Montalban X; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Institut de Recerca, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Rasche L; Department of Neurology, NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
  • Paul F; Department of Neurology, NeuroCure Clinical Research Center, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Berlin Institute of Health, Berlin, Germany.
  • González I; Experimental and Clinical Research Center, Charité-Universitätsmedizin Berlin, Max Delbrück Center for Molecular Medicine, Berlin, Germany.
  • Álvarez E; Neurology Department, Hospital Alvaro Cunqueiro, Vigo, Spain.
  • Ramo C; Neurology Department, Hospital Alvaro Cunqueiro, Vigo, Spain.
  • Caminero AB; Neurology Department, Hospital Germans Trias i Pujol, Badalona, Spain.
  • Aladro Y; Neurology Department, Hospital Nuestra Señora de Sonsoles, Avila, Spain.
  • Calles C; Neurology Department, Hospital Universitario Getafe, Getafe, Spain.
  • Eguía P; Neurology Department, Hospital Universitario Son Espases, Palma de Mallorca, Spain.
  • Belenguer-Benavides A; Neurology Department, Hospital Doctor Jose Molina Orosa, Arrecife, Spain.
  • Ramió-Torrentà L; Neurology Department, Hospital General Universitario de Castellón, Castellón, Spain.
  • Quintana E; Neurology Department, Hospital Universitario Doctor Josep Trueta, Girona, Spain.
  • Martínez-Rodríguez JE; Neurology Department, Hospital Universitario Doctor Josep Trueta, Girona, Spain.
  • Oterino A; Neurology Department, Hospital del Mar, Barcelona, Spain.
  • López de Silanes C; Neurology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
  • Casanova LI; Neurology Department, Hospital Universitario de Torrejón, Torrejón de Ardoz, Spain.
  • Landete L; Neurology Department, Hospital Universitario de Torrejón, Torrejón de Ardoz, Spain.
  • Frederiksen J; Neurology Department, Hospital Universitario Dr. Peset, Valencia, Spain.
  • Bsteh G; Glostrup Hospital, University of Copenhagen, Copenhagen, Denmark.
  • Mulero P; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Comabella M; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Institut de Recerca, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
  • Hernández MA; Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya, Vall d'Hebron Institut de Recerca, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Front Neurol ; 11: 579438, 2020.
Article em En | MEDLINE | ID: mdl-33408681
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.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article