POS0272 INTRAVENOUS VERSUS SUBCUTANEOUS TOCILIZUMAB IN A SERIES OF 471 PATIENTS WITH GIANT CELL ARTERITIS

نویسندگان

چکیده

Background Tocilizumab (TCZ) has shown efficacy in large-vessel vasculitis, including Giant Cell Arteritis (GCA) (1-3 ). Clinical trials with TCZ GCA was performed intravenous (iv) a phase 2 trial (3 ), and subcutaneous (sc) the 3 GiACTA (4 However, there are no studies comparing IV vs SC TCZ. Objectives To compare of patients according to route administration IV-TCZ SC-TCZ. Methods Multicentre study 471 diagnosed treated They were divided into groups administration: ) IV, b SC. by: ACR criteria, and/or temporal artery biopsy, c imaging techniques. Sustained remission established EULAR definitions (5 Results We studied (mean age, 74±9 years) TCZ, 238 233 SC-TCZ (Table 1). The time between diagnosis onset shorter group. Regarding acute reactants at beginning differences found both groups. There significant sustained or glucocorticoid-sparing effect (Figure Patients on treatment suffered more relevant adverse effects during follow-up. Table 1. Main characteristics tocilizumab (n= 238) (n=233) P Baseline Age(years), mean±SD 73.3±8.7 73.7±9.3 0.63 Sex, female/male (% female) 175/63 (73) 167/66 (72) 0.65 Time from (months), median [IQR] 8 [3-23.5] 5 [2-15] 0.016 ESR, mm 1st hour, 30.5 [12.5-53] 28 [10-56.5] 0.66 CRP, mg/dL, 1.4 [0.5-2.8] [0.4-4] 0.92 Prednisone dose, mg/day, 20 [10-40] [10-36.2] 0.69 Safety after Follow-up, 27 [16-44] 14 [6-26.7] <0.001 Relevant events, n 80 (34) 46 (19) events per 100 patients-year 12.7 15.2 NS Serious infections, 44 (18) 21 (9) 0.44 infections 6.7 7.2 MACEs, (%)/ 1 (0.4) 0 (0) - MACEs 0.1 Malignancies, 4 (1.7) 0.20 Malignancies 0.6 0.3 Abbreviations: CRP: C-reactive protein; ESR: erythrocyte sedimentation rate; GCA: giant cell arteritis; IQR: interquartile range; IV: intravenous; MACEs: major cardiovascular events; NS: non significant; SC: subcutaneous; SD: standard deviation Conclusion In GCA, seems equally effective safe regardless References [1]Calderón-Goercke M, et al. Semin Arthritis Rheum. 2019; 49: 126-135. PMID: 30655091 [2]Prieto-Peña D, Ther Adv Musculoskelet Dis. 2021; 13: 1759720X211020917. 34211589 [3]Villiger PM, Lancet. 2016; 387:1921-1927. 26952547 [4]Stone JH, N Engl J Med. 2017; 377:317-328. 28745999 Hellmich B, Ann Rheum 2020; 79: 19-30. 31270110 Disclosure Interests None declared

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

Design of the Tocilizumab in Giant Cell Arteritis Trial

Overview. The GiACTA trial is a multicenter, randomized, double-blind, and placebo-controlled study designed to test the ability of tocilizumab (TCZ), an interleukin (IL)-6 receptor antagonist, to maintain disease remission in patients with giant cell arteritis (GCA). Design. Approximately 100 centers will enroll 250 patients with active disease. The trial consists of a 52-week blinded treatmen...

متن کامل

Might tocilizumab be useful in patients with giant-cell arteritis and normal ESR?

We read with great interest the original article “Rapid induction of remission in large vessel vasculitis by IL-6 blockade” by Dr. Seitz et al. [1]. One of us (F.J.F-F) is very interested in the treatment of giant-cell arteritis because his mother was diagnosed with giant-cell arteritis 5 months previously. She had polymyalgia rheumatic for several months, and headache was the main manifestatio...

متن کامل

Relapses in Patients With Giant Cell Arteritis

Giant cell arteritis (GCA) is a relapsing disease. However, the nature, chronology, therapeutic impact, and clinical consequences of relapses have been scarcely addressed. We conducted the present study to investigate the prevalence, timing, and characteristics of relapses in patients with GCA and to analyze whether a relapsing course is associated with disease-related complications, increased ...

متن کامل

Phase III Study of the Efficacy and Safety of Subcutaneous Versus Intravenous Tocilizumab Monotherapy in Patients With Rheumatoid Arthritis

OBJECTIVE To evaluate the efficacious noninferiority of subcutaneous tocilizumab injection (TCZ-SC) monotherapy to intravenous TCZ infusion (TCZ-IV) monotherapy in Japanese patients with rheumatoid arthritis (RA) with an inadequate response to synthetic and/or biologic disease-modifying antirheumatic drugs (DMARDs). METHODS This study had a double-blind, parallel-group, double-dummy, comparat...

متن کامل

Efficacy and safety of subcutaneous tocilizumab versus intravenous tocilizumab in combination with traditional DMARDs in patients with RA at week 97 (SUMMACTA).

OBJECTIVES To evaluate the long-term efficacy and safety of subcutaneous (SC) tocilizumab (TCZ) versus intravenous (IV) TCZ, including switching formulations, in patients with rheumatoid arthritis (RA) and inadequate response to disease-modifying antirheumatic drugs (DMARDs). METHODS Patients (n=1262) were randomised 1:1 to receive TCZ-SC 162 mg weekly (qw)+placebo-IV every four weeks (q4w) o...

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: 2022

ISSN: ['1468-2060', '0003-4967']

DOI: https://doi.org/10.1136/annrheumdis-2022-eular.3260