POS0545 PRE-EXPOSURE PROPHYLAXIS OF COVID-19 WITH TIXAGEVIMAB AND CILGAVIMAB IN RHEUMATOLOGIC PATIENTS TREATED WITH RITUXIMAB: DATA FROM A SINGLE-CENTRE COHORT

نویسندگان

چکیده

Background Rheumatologic patients treated with Rituximab (RTX) are at higher risk of severe COVID-19 and death. The B-cell depletive treatment significantly affects B cell functions involved in anti-SARS-CoV-2 response, leading to relevant impacts on the clinical serological course infection, long-term immunity, vaccine responses. In light these observations, pre-exposure prophylaxis (PrEP) Tixagevimab Cilgavimab (TGM/CGM) was recently approved Italy for all RTX previous year, independently their status against SARS-CoV-2. Objectives We aimed evaluate efficacy safety TGM/CGM a single-centre cohort rheumatologic RTX. Methods From October 2022, who had been 12 months underwent assessment our tertiary centre were screened eligibility PrEP TGM/CGM. According indications Italian Medicines Agency (AIFA), we excluded subjects major cardiovascular factors and/or coagulation abnormalities; those reported allergic reaction any anti-COVID19 referred an allergologist evaluation before administration. Patients agreed be signed informed consent. Clinical demographic features collected baseline, follow-up phone performed day after 1 month administration, assess tolerability new COVID-19- related events. A descriptive analysis performed. Results 2022 31 December 90 Among them, 11 contraindications due comorbidities 55 refused receive COVID-19, 21 received 3 scheduled January2023. mean age 54 years (standard deviation: 17) 19 (90.5%) female; 9 affected by rheumatoid arthritis other diseases (3 systemic lupus erythematosus, 2 sclerosis, Sjögren syndrome, juvenile idiopathic arthritis, anti-synthetase vasculitides). Most them completed vaccination schedule (19, 90.5%) (42.8%) infectious event SARS-CoV-2 year. One no patient adverse events nor symptoms. Conclusion well tolerated population year symptoms observed Future observations may provide further data preventing COVID-19. REFERENCES: NIL. Acknowledgements: Disclosure Interests Maria Manara Speakers bureau: Novartis, Angelini, Consultant of: Lilly, MSD, Manuel Sette: None declared, Laura Giudice: Martina Biggioggero: Nicoletta Del Papa Janssen, Boehringer-Ingelheim, Actelion, Ennio Giulio Favalli AbbVie, BMS, Celltrion, Galapagos, Pfizer, UCB, Gerosa: Francesca Ingegnoli: Roberto Caporali Amgen, Fresenius, UCB.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Characteristics of late onset neutropenia in rheumatologic patients treated with rituximab: a case review analysis from a single center.

BACKGROUND Late onset neutropenia (LON) secondary to rituximab has been reported as an adverse event in the treatment of hematological malignancies but reports on autoimmune diseases are scarce. AIM To review the characteristics of LON in rheumatologic patients from a single center. DESIGN Retrospective case record study. METHODS Clinical and laboratory data since the introduction of ritu...

متن کامل

Routine pneumocystis pneumonia prophylaxis in patients treated with rituximab?

journal.publications.chestnet.org Figure 1. Proposed relationship among pulmonary infl ammation, systemic infl ammation, and COPDrelated comorbidities. *Statins have been shown to attenuate both pulmonary and systemic infl ammation through their effects on the innate immune response and NF k B/STAT3-mediated infl ammatory pathways. CRP 5 C-reactive protein; ETS 5 environmental tobacco smoke; M ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Annals of the Rheumatic Diseases

سال: 2023

ISSN: ['1468-2060', '0003-4967']

DOI: https://doi.org/10.1136/annrheumdis-2023-eular.4488