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FRI0270 (2020)
ONE-YEAR EFFECTIVENESS, RETENTION RATE AND SAFETY OF SECUKINUMAB IN ANKYLOSING SPONDYLITIS AND PSORIATIC ARTHRITIS: A REAL-LIFE MULTICENTRE STUDY
M. S. Chimenti1, G. L. Fonti1, P. Conigliaro1, F. Sunzini1, R. Scrivo2, L. Navarini3, P. Triggianese1, G. Peluso4, P. Scolieri5, R. Caccavale6, A. Picchianti-Diamanti7, E. De Martino1, S. Salemi7, D. Birra4, A. Altobelli2, M. Paroli6, V. Bruzzese5, B. Laganà7, E. Gremese4, F. Conti2, A. Afeltra3, R. Perricone1
1Rheumatology, Allergology and Clinical Immunology, University of Rome Tor Vergata, Rome, Italy
2Reumatologia, Dipartimento di Medicina Interna e Specialità Mediche, Sapienza Università di Roma, Rome, Italy
3Unit of Allergology, Immunology and Rheumatology, Department of Medicine, Università Campus Bio-Medico di Roma, Rome, Italy
4Istituto di Reumatologia e Scienze Affini Università Cattolica del Sacro Cuore- Fondazione Policlinico Universitario Agostino Gemelli – IRCCS- Presidio Columbus, Rome, Italy
5UOC di Medicina interna e Reumatologia, Ospedale Nuovo Regina Margherita, Rome, Italy
6Dipartimento di Scienze e Biotecnologie Medico-chirurgiche, Sapienza Università di Roma, Polo Pontino, Latina, Italy
7Department of Clinical and Molecular Medicine, Sant’Andrea University Hospital, Sapienza University of Rome, Rome, Italy

Background: Secukinumab (SEC) is the first interleukin-17A inhibitor showing efficacy in both ankylosing spondylitis (AS) and psoriatic arthritis (PsA) in randomised trials, but real-life data are lacking.


Objectives: In this prospective observational study, we evaluated the effectiveness and safety of SEC in patients with AS and PsA in a real-life setting.


Methods: From September 2018 to September 2019, data were collected from 168 consecutive outpatients at baseline (T0) and at 6 (T6) and 12 months (T12) after starting SEC (39 AS, 23%; 129 PsA, 77%).


Results: Significant improvement was seen at T6 and T12 for all clinical variables, including TJC, SJC, ESR, CRP, DAPSA, ASDAS-CRP, and BASDAI, as well as in patient-reported outcomes such as VAS-pain. By multivariable regression analysis, in AS patients high BASDAI at T0 correlated with diagnostic delay (R 2 =0.4; p=0.009) and peripheral joint involvement (R 2 =0.4; p=0.04). During follow-up, reduction of BASDAI positively correlated with high ESR (R 2 =0.65; p=0.04). ASDAS-CRP at T0 positively correlated with high ESR (R 2 =0.34; p=0.004). Reduction of ASDAS-CRP from T0 to T6 correlated with current smoking status (R 2 =0.42; p=0.0005). In PsA patients, reduction of DAPSA score from T0 to T12 negatively correlated with the presence of metabolic syndrome (R 2 =0.41; p= 0.0025). Retention rate showed good drug survival and an influence of female sex ( Figure 1 ) in the survival curve in only AS patients, but no differences based on BMI, gender and lines of treatment were observed ( Figure 2 ). SEC was well tolerated: Eleven patients discontinued treatment for non-severe adverse events.


Conclusion: We demonstrated the effectiveness and safety of SEC in patients with AS and PsA in a real-life setting for the first time. No gender differences were observed; however, less clinical improvement was seen in smokers and in patients with metabolic syndrome


REFERENCES:

No references.


Disclosure of Interests: Maria Sole Chimenti: None declared, giulia lavinia fonti: None declared, Paola Conigliaro: None declared, flavia sunzini: None declared, Rossana Scrivo: None declared, luca navarini: None declared, paola triggianese: None declared, giusy peluso: None declared, Palma Scolieri: None declared, rosalba caccavale: None declared, Andrea Picchianti-Diamanti: None declared, erica de martino: None declared, simonetta salemi: None declared, domenico birra: None declared, Alessio Altobelli: None declared, marino paroli: None declared, Vincenzo Bruzzese: None declared, Bruno Laganà: None declared, Elisa Gremese Speakers bureau: Abbvie, BMS, Celgene, Jannsen, Lilly, MSD, Novartis, Pfizer, Sandoz, UCB, fabrizio conti Speakers bureau: BMS, Lilly, Abbvie, Pfizer, Sanofi, Antonella Afeltra: None declared, Roberto Perricone: None declared


Citation: Ann Rheum Dis, volume 79, supplement 1, year 2020, page 716
Session: Spondyloarthritis - treatment (Poster Presentations)