Safety of Ixekizumab Treatment for up to 5 Years in Adult Patients with Moderate-to-Severe Psoriasis: Results from Greater Than 17,000 Patient-Years of Exposure.
Adverse events
Etanercept
IL-17
Integrated analysis
Ixekizumab
Psoriasis
Safety
Journal
Dermatology and therapy
ISSN: 2193-8210
Titre abrégé: Dermatol Ther (Heidelb)
Pays: Switzerland
ID NLM: 101590450
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
received:
08
08
2019
pubmed:
22
11
2019
medline:
22
11
2019
entrez:
22
11
2019
Statut:
ppublish
Résumé
Long-term safety data are critical for evaluating therapies for psoriasis. Ixekizumab has demonstrated efficacy and is well tolerated for the treatment of moderate-to-severe plaque psoriasis. We examined the safety and tolerability of up to 5 years of ixekizumab therapy in patients with psoriasis. Integrated safety data were analyzed from 13 ixekizumab clinical studies. Rates of treatment-emergent adverse events (TEAEs), serious AEs (SAEs) and AEs of special interest were analyzed for the 12-week induction period in the combined pivotal studies, and for all pooled studies by year(s) of therapy and overall, reported as exposure-adjusted incidence rates (IRs) per 100 patient-years (p-y) and/or frequencies. Total ixekizumab exposure was 17,003.4 p-y (N = 5898); 2749 patients had ≥ 4 years of exposure. When compared across years of exposure, rates for AEs remained largely stable or declined, including TEAEs leading to discontinuation (3.8/100 p-y in year 1, declining to 2.0/100 p-y in year 5); SAEs (range 6.2-7.0/100 p-y); serious infections (range 1.3-1.7/100 p-y); nonmelanoma skin cancer (ranging from 0.5/100 p-y in year 1 to 0.2/100 p-y in years 4-5); other malignancies (range 0.4-0.6/100 p-y); inflammatory bowel disease including ulcerative colitis and Crohn's disease (IR 0.2/100 p-y); and major adverse cardiovascular events (MACE) (range 0.3-0.7/100 p-y). Candidiasis was reported in 327 patients (IR 1.9/100 p-y), with the majority identified as mucocutaneous. The rate of injection site reactions was 15.5/100 p-y during year 1 and 2.0-2.3/100 p-y by years 3-5. The decrease in rates of TEAEs and the stable rates of SAEs, other malignancies and MACE during up to 5 years of ixekizumab dosing are consistent with previous reports describing a favorable safety profile of ixekizumab following shorter durations of exposure. Eli Lilly and Company.
Identifiants
pubmed: 31749092
doi: 10.1007/s13555-019-00340-3
pii: 10.1007/s13555-019-00340-3
pmc: PMC6994584
doi:
Types de publication
Journal Article
Langues
eng
Pagination
133-150Références
J Am Acad Dermatol. 2017 Mar;76(3):432-440.e17
pubmed: 27889292
Eur J Immunol. 2012 Sep;42(9):2246-54
pubmed: 22949323
J Am Acad Dermatol. 2012 Feb;66(2):e33-45
pubmed: 20850895
Lancet. 2015 Sep 5;386(9997):983-94
pubmed: 26025581
J Inflamm Res. 2016 Apr 19;9:39-50
pubmed: 27143947
J Am Acad Dermatol. 2019 Jan;80(1):27-40
pubmed: 30017705
J Drugs Dermatol. 2018 Feb 1;17(2):200-206
pubmed: 29462229
Am J Clin Dermatol. 2011 Oct 1;12(5):321-37
pubmed: 21834597
Gastroenterology. 2011 May;140(6):1756-1767
pubmed: 21530742
N Engl J Med. 2005 Nov 24;353(21):2262-9
pubmed: 16306523
J Invest Dermatol. 2009 Nov;129(11):2604-12
pubmed: 19440219
Nat Immunol. 2009 Jun;10(6):603-9
pubmed: 19448631
Br J Dermatol. 1999 Feb;140(2):237-42
pubmed: 10233215
Arterioscler Thromb Vasc Biol. 2015 Feb;35(2):258-64
pubmed: 25234818
Lancet. 2015 Aug 8;386(9993):541-51
pubmed: 26072109
Rheumatology (Oxford). 2010 Feb;49(2):295-307
pubmed: 19946022
Gut. 1994 Oct;35(10):1433-8
pubmed: 7959201
Br J Dermatol. 2018 Oct;179(4):844-852
pubmed: 29747232
Br J Dermatol. 2019 Jan;180(1):76-85
pubmed: 30169904
J Am Acad Dermatol. 2017 Mar;76(3):441-448.e2
pubmed: 28027825
N Engl J Med. 2016 Jul 28;375(4):345-56
pubmed: 27299809
Infect Immun. 2010 Jan;78(1):32-8
pubmed: 19901061
Eur Heart J. 2010 Apr;31(8):1000-6
pubmed: 20037179
Am J Cardiol. 2011 Nov 1;108(9):1362-70
pubmed: 21855836
Br J Dermatol. 2008 Sep;159(4):895-902
pubmed: 18616778
JAMA. 2006 Oct 11;296(14):1735-41
pubmed: 17032986
Am J Med. 2011 Aug;124(8):775.e1-6
pubmed: 21787906
Am J Gastroenterol. 2016 Nov;111(11):1599-1607
pubmed: 27481309
Gut. 2003 Jan;52(1):65-70
pubmed: 12477762
Br J Dermatol. 2010 Sep;163(3):586-92
pubmed: 20633008
Br J Dermatol. 2011 Nov;165(5):1066-73
pubmed: 21777216
J Eur Acad Dermatol Venereol. 2018 Aug;32(8):1320-1326
pubmed: 29573294
Br J Dermatol. 2013 Apr;168(4):844-54
pubmed: 23301632
J Rheumatol. 2010 Nov;37(11):2205-15
pubmed: 20810498
J Am Acad Dermatol. 2019 Jan;80(1):43-53
pubmed: 30017706
Br J Dermatol. 2017 Oct;177(4):1014-1023
pubmed: 28542874
J Eur Acad Dermatol Venereol. 2019 Feb;33(2):333-339
pubmed: 30198588
Br J Dermatol. 2018 Oct;179(4):853-862
pubmed: 29782642
Nat Immunol. 2018 Jul;19(7):755-765
pubmed: 29915298
Gut. 2012 Dec;61(12):1693-700
pubmed: 22595313
Immunol Res. 2011 Aug;50(2-3):181-7
pubmed: 21717069
J Am Acad Dermatol. 2014 Mar;70(3):512-6
pubmed: 24388724
Rheumatology (Oxford). 2011 Mar;50(3):518-31
pubmed: 21071477
J Am Acad Dermatol. 2009 Jun;60(6):1001-17
pubmed: 19344980
Science. 2011 Apr 1;332(6025):65-8
pubmed: 21350122