Adverse Events in Giant Cell Arteritis and Rheumatoid Arthritis Patient Populations: Analyses of Tocilizumab Clinical Trials and Claims Data

被引:19
作者
Gale, Sara [1 ]
Huong Trinh [1 ]
Tuckwell, Katie [1 ]
Collinson, Neil [2 ]
Stone, John H. [3 ]
Sarsour, Khaled [1 ]
Pei, Jinglan [1 ]
Best, Jennie [1 ]
Birchwood, Christine [1 ]
Mohan, Shalini V. [1 ]
机构
[1] Genentech Inc, San Francisco, CA 94080 USA
[2] Roche Prod Ltd, Welwyn Garden City, Herts, England
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
关键词
Giant cell arteritis; Rheumatoid arthritis; Rheumatology; Safety; Tocilizumab; MODIFYING ANTIRHEUMATIC DRUGS; INTERLEUKIN-6 RECEPTOR INHIBITION; DOUBLE-BLIND; SUBCUTANEOUS TOCILIZUMAB; GLUCOCORTICOID THERAPY; TREATMENT OUTCOMES; DISEASE; COMBINATION; MANAGEMENT; PLACEBO;
D O I
10.1007/s40744-019-0139-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionThe safety profile of tocilizumab (TCZ) in patients with rheumatoid arthritis (RA) is well established. TCZ was approved to treat giant cell arteritis (GCA) in 2017 in the USA and Europe, and its safety profile in patients with GCA continues to be defined. The objective of this analysis was to examine incidence rates (IRs) of adverse events of special interest (AESI) occurring during the TCZ clinical development program and in healthcare claims data in patients with GCA or RA.MethodsTCZ-naive patients with GCA or RA were identified in the MarketScan administrative healthcare claims database. TCZ-treated patients with GCA from the GiACTA trial and TCZ-treated patients with RA from pooled clinical trial data were analyzed. The IRs of AESI (AESI IRs) were calculated for all cohorts. In the claims cohorts, risks of AESI were estimated using Poisson regression.ResultsTCZ-naive claims cohorts comprised 4804 patients with GCA [mean (standard deviation) age 73.4 (9.8) years; follow-up 3.9 (3.1) years] and 15,164 patients with RA [age 60.3 (8.2)years; follow-up, 4.5 (2.8) years]. TCZ-treated clinical trial cohorts comprised 149patients with GCA [age 69.5 (8.4) years; exposure approx.138 patient-years (PY)] and 7647 with RA [age 52 (12.6) years; exposure approx.22,394 PY]. The IRs of infections, stroke, malignancies, myocardial infarction, and gastrointestinal perforations in the GCA claims cohort exceeded those in the RA claims cohort; the risk of AESI (adjusted for age and glucocorticoid use) was higher in patients with GCA than in those with RA. Similar patterns to the claims cohorts in terms of the AESI IRs were observed in clinical trial cohorts, although the number of events was limited in the GCA trial cohort.ConclusionHigher IRs of AESI were observed in patients with GCA versus those with RA in both TCZ-naive and -treated cohorts. Differences in underlying disease, age, and glucocorticoid use may influence AESI incidence, irrespective of intervention.FundingThis study was funded by F. Hoffmann-La Roche Ltd and Genentech, Inc. Article processing charges were funded by F. Hoffmann-La Roche Ltd.Plain Language SummaryPlain language summary is available for this article.
引用
收藏
页码:77 / 88
页数:12
相关论文
共 40 条
  • [1] Increased risk of cardiovascular disease in giant cell arteritis: a general population-based study
    Amiri, Neda
    De Vera, Mary
    Choi, Hyon K.
    Sayre, Eric C.
    Avina-Zubieta, J. Antonio
    [J]. RHEUMATOLOGY, 2016, 55 (01) : 33 - 40
  • [2] ANDERSSON R, 1986, ACTA MED SCAND, V220, P465
  • [3] Risk of Cardiovascular Mortality in Patients With Rheumatoid Arthritis: A Meta-Analysis of Observational Studies
    Avina-Zubieta, J. Antonio
    Choi, Hyon K.
    Sadatsafavi, Mohsen
    Etminan, Mahyar
    Esdaile, John M.
    Lacaille, Diane
    [J]. ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2008, 59 (12): : 1690 - 1697
  • [4] Association Between Glucocorticoid Exposure and Healthcare Expenditures for Potential Glucocorticoid-related Adverse Events in Patients with Rheumatoid Arthritis
    Best, Jennie H.
    Kong, Amanda M.
    Lenhart, Gregory M.
    Sarsour, Khaled
    Stott-Miller, Marni
    Hwang, Yong
    [J]. JOURNAL OF RHEUMATOLOGY, 2018, 45 (03) : 320 - 328
  • [5] Corticosteroid-related adverse events in patients with giant cell arteritis: A claims-based analysis
    Broder, Michael S.
    Sarsour, Khaled
    Chang, Eunice
    Collinson, Neil
    Tuckwell, Katie
    Napalkov, Pavel
    Klearman, Micki
    [J]. SEMINARS IN ARTHRITIS AND RHEUMATISM, 2016, 46 (02) : 246 - 252
  • [6] Tocilizumab in early progressive rheumatoid arthritis: FUNCTION, a randomised controlled trial
    Burmester, Gerd R.
    Rigby, William F.
    van Vollenhoven, Ronald F.
    Kay, Jonathan
    Rubbert-Roth, Andrea
    Kelman, Ariella
    Dimonaco, Sophie
    Mitchell, Nina
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2016, 75 (06) : 1081 - 1091
  • [7] A randomised, double-blind, parallel-group study of the safety and efficacy of subcutaneous tocilizumab versus intravenous tocilizumab in combination with traditional disease-modifying antirheumatic drugs in patients with moderate to severe rheumatoid arthritis (SUMMACTA study)
    Burmester, Gerd R.
    Rubbert-Roth, Andrea
    Cantagrel, Alain
    Hall, Stephen
    Leszczynski, Piotr
    Feldman, Daniel
    Rangaraj, Madura J.
    Roane, Georgia
    Ludivico, Charles
    Lu, Peng
    Rowell, Lucy
    Bao, Min
    Mysler, Eduardo F.
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 (01) : 69 - 74
  • [8] Caplan L, 2007, J RHEUMATOL, V34, P696
  • [9] The incidence of giant cell arteritis in Olmsted County, Minnesota, over a 60-year period 1950-2009
    Chandran, A. K.
    Udayakumar, P. D.
    Crowson, C. S.
    Warrington, K. J.
    Matteson, E. L.
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2015, 44 (03) : 215 - 218
  • [10] BSR and BHPR guidelines for the management of giant cell arteritis
    Dasgupta, Bhaskar
    Borg, Frances A.
    Hassan, Nada
    Alexander, Leslie
    Barraclough, Kevin
    Bourke, Brian
    Fulcher, Joan
    Hollywood, Jane
    Hutchings, Andrew
    James, Pat
    Kyle, Valerie
    Nott, Jennifer
    Power, Michael
    Samanta, Ash
    [J]. RHEUMATOLOGY, 2010, 49 (08) : 1594 - 1597