| Title: |
MACE and VTE Across Upadacitinib Clinical Trial Programs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis |
| Authors: |
Charles-Schoeman, Christina; Choy, Ernest; McInnes, Iain B; Mysler, Eduardo; Nash, Peter; Yamaoka, Kunihiro; Lippe, Ralph; Khan, Nasser; Shmagel, Anna K; Palac, Hannah; Suboticki, Jessica; Curtis, Jeffrey |
| Publisher Information: |
Wiley |
| Publication Year: |
2022 |
| Collection: |
Griffith University: Griffith Research Online |
| Subject Terms: |
Clinical sciences; Rheumatology and arthritis; Cardiovascular medicine and haematology; Life Sciences & Biomedicine; Rheumatology; Science & Technology |
| Subject Geographic: |
USA |
| Time: |
2022-11-10 to 2022-11-14; Philadelphia, USA |
| Description: |
Background/Purpose: Patients with untreated immune-mediated inflammatory diseases, such as RA, PsA, and AS, are at increased risk for major adverse cardiovascular events (MACE) and venous thromboembolic events (VTE) compared with the general population. The purpose of this analysis was to describe the events and risk factors for MACE and VTE in the RA, PsA, and AS clinical trial programs of the Janus kinase (JAK) inhibitor, upadacitinib (UPA). Methods: Treatment-emergent adverse events (TEAEs) of MACE and VTE from 9 (6 RA; 2 PsA; 1 AS) pivotal, randomized, controlled, phase 2b/3 trials were summarized for UPA 15 mg (approved rheumatology dose), UPA 30 mg, adalimumab (ADA) 40 mg, and MTX. TEAEs were defined as onset on or after the first dose of study drug and up to 30 or 70 days after last dose for UPA/MTX or ADA, respectively. TEAEs of MACE (cardiovascular [CV] death, non-fatal myocardial infarction, and non-fatal stroke) and VTE (pulmonary embolism [PE] and deep vein thrombosis [DVT]) were adjudicated by a blinded, independent cardiovascular adjudication committee. Patients were not censored at the time of event; data are presented as exposure adjusted event rates (EAERs) in events per 100 patient-years (E/100 PY), with a cutoff date of 30 June 2021. Time-to-event was analyzed using the Kaplan-Meier method, and EAERs were evaluated over 6-month increments. Given the limited number of events, Cox-regression were limited to univariable analyses and assessed the relationship between potential risk factors and occurrence of MACE and VTE in patients receiving UPA. Results: Across trials, 4298 patients received ≥ 1 dose of UPA 15 mg and 2125 received UPA 30 mg, 1008 patients received ADA 40 mg, and 314 patients received MTX. At baseline, 40%–50% of patients had 2 or more CV risk factors, and the proportion of patients ≥ 65 years ranged from 6%–23%. EAERs of MACE and VTE in RA and PsA are presented in Figure 1, with 0 MACE and 1 VTE (PE) reported in AS. Of the 41 MACE reported in the UPA 15 mg group across RA and ... |
| Document Type: |
conference object |
| Language: |
English |
| Relation: |
Arthritis & Rheumatology; ACR Convergence 2022; Charles-Schoeman, C; Choy, E; McInnes, IB; Mysler, E; Nash, P; Yamaoka, K; Lippe, R; Khan, N; Shmagel, AK; Palac, H; Suboticki, J; Curtis, J, MACE and VTE Across Upadacitinib Clinical Trial Programs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis, Arthritis & Rheumatology, 2022, 74 (S9), pp. 1016-1019; https://hdl.handle.net/10072/421209 |
| Availability: |
https://hdl.handle.net/10072/421209 |
| Rights: |
open access |
| Accession Number: |
edsbas.5793F1F5 |
| Database: |
BASE |