Tocilizumab in refractory Caucasian Takayasu's arteritis: a multicenter study of 54 patients and literature review


Por: Prieto-Pena, D, Bernabeu, P, Vela, P, Narvaez, J, Fernandez-Lopez, J, Freire-Gonzalez, M, Gonzalez-Alvarez, B, Solans-Laque, R, Rubio, J, Ortego, N, Fernandez-Diaz, C, Rubio, E, Garcia-Morillo, S, Minguez, M, Fernandez C, de Miguel, E, Melchor, S, Salgado, E, Bravo, B, Romero-Yuste, S, Salvatierra, J, Hidalgo, C, Manrique, S, Romero-Gomez, C, Moya, P, Alvarez-Rivas, N, Mendizabal, J, Ortiz-Sanjuan, F, de Pedro, I, Alonso-Valdivielso, J, Perez-Sanchez, L, Roldan, R, Fernandez-Llanio, N, de la Torre, R, Suarez, S, Cabrera, M, Sanchez, M, Loricera, J, Atienza-Mateo, B, Castaneda, S, Gonzalez-Gay, M and Blanco, R

Publicada: 1 jun 2021
Categoría: Orthopedics and sports medicine

Resumen:
Objective: To assess the efficacy and safety of tocilizumab (TCZ) in Caucasian patients with refractory Takayasu's arteritis (TAK) in clinical practice. Methods: A multicenter study of Caucasian patients with refractory TAK who received TCZ. The outcome variables were remission, glucocorticoid-sparing effect, improvement in imaging techniques, and adverse events. A comparative study between patients who received TCZ as monotherapy (TCZ(MONO)) and combined with conventional disease modifying anti-rheumatic drugs (cDMARDs) (TCZ(COMBO)) was performed. Results: The study comprised 54 patients (46 women/8 men) with a median [interquartile range (IQR)] age of 42.0 (32.5-50.5) years. TCZ was started after a median (IQR) of 12.0 (3.0-31.5) months since TAK diagnosis. Remission was achieved in 12/54 (22.2%), 19/49 (38.8%), 23/44 (52.3%), and 27/36 (75%) patients at 1, 3, 6, and 12 months, respectively. The prednisone dose was reduced from 30.0 mg/day (12.5-50.0) to 5.0 (0.0-5.6) mg/day at 12 months. An improvement in imaging findings was reported in 28 (73.7%) patients after a median (IQR) of 9.0 (6.0-14.0) months. Twenty-three (42.6%) patients were on TCZ(MONO) and 31 (57.4%) on TCZ(COMBO): MTX (n = 28), cyclosporine A (n = 2), azathioprine (n = 1). Patients on TCZ(COMBO) were younger [38.0 (27.0-46.0) versus 45.0 (38.0-57.0)] years; difference (diff) [95% confidence interval (CI) = -7.0 (-17.9, -0.56] with a trend to longer TAK duration [21.0 (6.0-38.0) versus 6.0 (1.0-23.0)] months; diff 95% CI = 15 (-8.9, 35.5), and higher c-reactive protein [2.4 (0.7-5.6) versus 1.3 (0.3-3.3)] mg/dl; diff 95% CI = 1.1 (-0.26, 2.99). Despite these differences, similar outcomes were observed in both groups (log rank p = 0.862). Relevant adverse events were reported in six (11.1%) patients, but only three developed severe events that required TCZ withdrawal. Conclusion: TCZ in monotherapy, or combined with cDMARDs, is effective and safe in patients with refractory TAK of Caucasian origin.

Filiaciones:
Prieto-Pena, D:
 Hosp Univ Marques de Valdecilla, Dept Rheumatol, IDIVAL, Res Grp Genet Epidemiol & Atherosclerosis Syst Di, Santander, Spain

Bernabeu, P:
 Hosp Gen Alicante, Dept Rheumatol, Alicante, Spain

Vela, P:
 Hosp Gen Alicante, Dept Rheumatol, Alicante, Spain

Narvaez, J:
 Hosp Bellvitge Princeps Espanya, Dept Rheumatol, Barcelona, Spain

Fernandez-Lopez, J:
 Complejo Hosp Univ A Coruna, Dept Rheumatol, La Coruna, Spain

Freire-Gonzalez, M:
 Complejo Hosp Univ A Coruna, Dept Rheumatol, La Coruna, Spain

Gonzalez-Alvarez, B:
 Hosp Nuestra Senora Candelaria, Dept Rheumatol, Tenerife, Spain

Solans-Laque, R:
 Hosp Valle De Hebron, Dept Internal Med, Barcelona, Spain

Rubio, J:
 Hosp San Cecilio, Autoimmune Dis Unit, Granada, Spain

Ortego, N:
 Hosp San Cecilio, Autoimmune Dis Unit, Granada, Spain

Fernandez-Diaz, C:
 Hosp Univ Princesa, Dept Rheumatol, IIS Princesa, Madrid, Spain

Rubio, E:
 Hosp Virgen Rocio, Autoimmune Dis Unit, Seville, Spain

Garcia-Morillo, S:
 Hosp Virgen Rocio, Autoimmune Dis Unit, Seville, Spain

:
 Hosp San Juan Alicante, Dept Rheumatol, Alicante, Spain

Fernandez C:
 Hosp San Juan Alicante, Dept Rheumatol, Alicante, Spain

de Miguel, E:
 Hosp Univ La Paz, Dept Rheumatol, Madrid, Spain

Melchor, S:
 Hosp Univ 12 Octubre, Dept Rheumatol, Madrid, Spain

Salgado, E:
 Complejo Hosp Univ Ourense, Dept Rheumatol, Orense, Spain

Bravo, B:
 Hosp Virgen Nieves, Dept Rheumatol, Granada, Spain

Romero-Yuste, S:
 Complejo Hosp Univ Pontevedra, Dept Rheumatol, Pontevedra, Spain

Salvatierra, J:
 Hosp San Cecilio, Autoimmune Dis Unit, Granada, Spain

Hidalgo, C:
 Complejo Univ Salamanca, Dept Rheumatol, Salamanca, Spain

Manrique, S:
 Hosp Reg Malaga, Autoimmune Dis Unit, Malaga, Spain

Romero-Gomez, C:
 Hosp Reg Malaga, Autoimmune Dis Unit, Malaga, Spain

Moya, P:
 Hosp Santa Creu & Sant Pau, Dept Rheumatol, Barcelona, Spain

Alvarez-Rivas, N:
 Hosp Univ San Agustin, Dept Rheumatol, Aviles, Spain

Mendizabal, J:
 Complejo Hosp Navarra, Dept Rheumatol, Pamplona, Spain

Ortiz-Sanjuan, F:
 Hosp Univ & Politecn La Fe, Dept Rheumatol, Valencia, Spain

de Pedro, I:
 Hosp Carlos Haya, Autoimmune Dis Unit, Malaga, Spain

Alonso-Valdivielso, J:
 Hosp Univ Burgos, Dept Rheumatol, Burgos, Spain

Perez-Sanchez, L:
 Hosp Univ Reina Sofia, Dept Rheumatol, Cordoba, Spain

Roldan, R:
 Hosp Univ Reina Sofia, Dept Rheumatol, Cordoba, Spain

:
 Hosp Arnau Vilanova, Dept Rheumatol, Valencia, Spain

de la Torre, R:
 Hosp Univ Cent Asturias, Autoimmune Dis Unit, Oviedo, Spain

Suarez, S:
 Hosp Univ Cent Asturias, Autoimmune Dis Unit, Oviedo, Spain

Cabrera, M:
 Hosp Nuestra Senora Candelaria, Dept Rheumatol, Tenerife, Spain

Sanchez, M:
 Hosp Nuestra Senora Candelaria, Dept Rheumatol, Tenerife, Spain

Loricera, J:
 Hosp Univ Marques de Valdecilla, Dept Rheumatol, IDIVAL, Res Grp Genet Epidemiol & Atherosclerosis Syst Di, Santander, Spain

Atienza-Mateo, B:
 Hosp Univ Marques de Valdecilla, Dept Rheumatol, IDIVAL, Res Grp Genet Epidemiol & Atherosclerosis Syst Di, Santander, Spain

Castaneda, S:
 Hosp Univ Princesa, Dept Rheumatol, IIS Princesa, Madrid, Spain

 Univ Autonoma Madrid IUAMI, UAM ROCHE, EPID Future, Madrid, Spain

Gonzalez-Gay, M:
 Hosp Univ Marques de Valdecilla, Rheumatol Div, Res Grp Genet Epidemiol & Atherosclerosis Syst Di, IDIVAL, Ave Valdecilla S-N, Santander 39008, Spain

 Univ Cantabria, Sch Med, Santander, Spain

 Univ Witwatersrand, Fac Hlth Sci, Sch Physiol, Cardiovasc Pathophysiol & Genom Res Unit, Johannesburg, South Africa

Blanco, R:
 Hosp Univ Marques de Valdecilla, Dept Rheumatol, IDIVAL, Res Grp Genet Epidemiol & Atherosclerosis Syst Di, Santander, Spain
ISSN: 1759720X





THERAPEUTIC ADVANCES IN MUSCULOSKELETAL DISEASE
Editorial
SAGE Publications Inc., 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND, Estados Unidos America
Tipo de documento: Review
Volumen: 13 Número:
Páginas:
WOS Id: 000688092300001
ID de PubMed: 34211589
imagen Green Published, gold

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