Hospital Universitario Marqués de Valdecilla Santander, Spain
Julio Sánchez-Martín1, Javier Loricera1, Santos Castañeda2, Clara Moriano3, F. Javier Narváez4, Vicente Aldasoro5, Olga Maiz6, Rafael Melero7, Juan Ignacio Villa Blanco8, Paloma Vela-Casampere9, Susana Romero Yuste10, José Luis Callejas11, Eugenio De Miguel12, Eva Galíndez-Agirregoikoa13, Francisca Sivera14, Jesus Fernandez15, Carles Galisteo16, Ivan Ferraz Amaro17, Lara Sánchez-Bilbao1, Monica Calderon-Goercke18, Miguel Ángel González-Gay19 and Ricardo Blanco20, 1Hospital Universitario Marqués de Valdecilla, Santander, Spain, 2Division of Rheumatology, Hospital Universitario de La Princesa, IIS-Princesa, Madrid, Spain, 3Complejo Asistencial Universitario de León, León, Spain, 4Rheumatology Department, Hospital Universitario de Bellvitge, Barcelona, Spain, 5Hospital Universitario de Navarra, Pamplona, Spain, 6Hospital Universitario de Donostia, San Sebastián, Spain, 7Complexo Hospitalario Universitario de Vigo, Vigo, Spain, 8Sierrallana Hospital, Torrelavega, Spain, 9Hospital General Universitario Alicante, Alicante, Spain, 10Complexo Hospitalario Universitario, Pontevedra, Spain, 11Hospital San Cecilio, Granada, Spain, 12Hospital Universitario La Paz, Madrid, Spain, 13Basurto University Hospital, Bilbao, Spain, 14Hospital Universitario de Elda, San Vicente del Raspeig, Spain, 15Hospital de La Coruña, La Coruña, Spain, 16Hospital Parc Tauli,, Sabadel, Spain, 17Division of Rheumatology. Hospital Universitario de Canarias. Spain., Santa Cruz de Tenerife, Spain, 18Hospital de Sierrallana, Torrelavega, Spain, 19Department of Medicine and Psychiatry, Universidad de Cantabria; Rheumatology Division, Hospital Universitario Marqués de Valdecilla; Research group on genetic epidemiology and atherosclerosis in systemic diseases and in metabolic diseases of the musculoskeletal system, IDIVAL, Santander, Spain. Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa, 20Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain
Background/Purpose: Positron emission tomography (PET) is one of the tools available for the diagnosis of extracranial large-vessel vasculitis (1-5). Tocilizumab (TCZ) has shown efficacy in large-vessel vasculitis (LVV) including GCA. However, the improvement objectified by imaging techniques after TCZ therapy in extracranial GCA patients is controversial.
The purpose of this study is to assess the effectiveness of TCZ improving the wall vessel inflammation by PET in GCA patients with large-vessel involvement.
Methods: Observational, multicenter study of 101 GCA patients treated with TCZ. GCA was diagnosed according to: a) ACR criteria, and/or b) biopsy of temporal artery, and/or c) presence of signs of vessel wall inflammation by PET, defined by the presence of vascular wall uptake of Fluorodeoxyglucose (FDG). Patients were divided into two subgroups: a) with, and b) without signs of improvement (partial or total) in the follow-up PET.
Results: We studied 101 patients (74 women/27 men; mean age 69.7±9.3 years). Main clinical features of GCA with and without PET improvement are shown in TABLE. The group of patients which experienced PET improvement was older and was receiving higher doses of corticosteroids at TCZ onset.
Conclusion: TCZ seems to be effective controlling GCA including vascular involvement detected by PET. However, the improvement observed by PET is most often partial, and rarely complete.
References:
Loricera J, et al. Rev Esp Med Nucl Imagen Mol. 2015; 34: 372-7. PMID: 26272121
Main features of 101 GCA patients treated with tocilizumab and with presence of signs of vessel wall inflammation by PET.
Improvement by PET according to the time of the test. Disclosures: J. Sánchez-Martín, None; J. Loricera, None; S. Castañeda, Roche; C. Moriano, None; F. Narváez, None; V. Aldasoro, None; O. Maiz, None; R. Melero, None; J. Villa Blanco, None; P. Vela-Casampere, None; S. Romero Yuste, Pfizer, Lilly, AbbVie, Biogen, Sanofi; J. Callejas, None; E. De Miguel, None; E. Galíndez-Agirregoikoa, None; F. Sivera, None; J. Fernandez, None; C. Galisteo, None; I. Ferraz Amaro, AbbVie/Abbott, Merck/MSD, Janssen, Roche, AbbVie/Abbott, Pfizer, Roche, Amgen, Celgene, Merck/MSD; L. Sánchez-Bilbao, Eli Lilly; M. Calderon-Goercke, None; M. González-Gay, AbbVie/Abbott, Merck/MSD, Janssen, Roche, AbbVie/Abbott, Roche, Sanofi, Eli Lilly, Celgene, Sobi, Merck/MSD; R. Blanco, Eli Lilly, Pfizer, Roche, Janssen, MSD, AbbVie, Amgen, AstraZeneca, Bristol Myers Squibb, Galapagos, Novartis, Sanofi.