Efficacy and safety of mirikizumab in psoriasis: a systematic review and meta-analysis of randomized controlled trials

被引:0
|
作者
Pereira, Mable [1 ]
Franco, Ancy Jenil [2 ]
Chintharala, Karthik [3 ]
Vieira, Ana Carolina Putini [4 ]
de Jesus, Ana Carolina Ventura de Santana [5 ]
Lajczak, Pawel [6 ]
Alhwaishel, Khaled [7 ]
Castaneda, Mario Saul Lira [8 ]
Weba, Elizabet Taylor Pimenta [9 ]
Reich, Kristian [10 ]
机构
[1] Lincoln Amer Univ, Sch Med, 8A & 8B,Water & Barrack St, Kingston 413741, Guyana
[2] Sri Muthukumaran Med Coll Hosp & Res Inst, Near Mangadu,Kundrathur Main Rd, Chennai, Tamil Nadu, India
[3] NRI Acad Med Sci, Guntur 522503, Andhra Pradesh, India
[4] Univ Santo Amaro, 340,Rua Prof Eneas Siqueira Neto, Sao Paulo, SP, Brazil
[5] Bahiana Sch Med & Publ Hlth, Escola Bahiana Med & Saude Publ, Ave Dom Joao VI, 275, Brotas, BR-40290000 Salvador, BA, Brazil
[6] Med Univ Siles, Dept Biochem, Jordana 19, PL-41808 Zabrze, Poland
[7] Univ Mansoura, Fac Med, Manchester Program Med Educ, El Gomhouria St, Mansoura 35516, Dakahlia, Egypt
[8] Univ Juarez Estado Durango, Fac Med & Nutr, Univ & Fanny Anitua s-n, Durango 34000, Dgo, Mexico
[9] State Univ Regiao Tocantina Maranhao, Godofredo Viana St,1300 Ctr, BR-65900000 Imperatriz, MA, Brazil
[10] Univ Med Ctr Hamburg Eppendorf, Inst Hlth Serv Res Dermatol & Nursing, Translat Res Inflammatory Skin Dis, Hamburg, Germany
关键词
Mirikizumab; Interleukin-23; inhibitor; Psoriasis;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction Mirikizumab, an interleukin-23 (IL-23) p19 subunit inhibitor, has emerged as a promising treatment for moderate-to-severe plaque psoriasis. Despite its promising results, a comprehensive synthesis of clinical data is essential to assess its overall efficacy and safety profile. Methods We searched PubMed, Embase, and Cochrane for studies assessing mirikizumab in moderate-to-severe psoriasis. A random-effects model using Inverse Variance (IV) computed mean differences (MD) for continuous outcomes and risk ratios (RR) for binary endpoints. Risk Difference (RD) studies were analysed using generic inverse variance (GIV) in Review Manager. Statistical analyses were conducted using R software version 4.2.1, following PRISMA guidelines. Results This analysis of three RCTs involving 1,649 adult patients over 16-52 weeks demonstrated mirikizumab's significant efficacy in treating psoriasis. At 16 weeks, mirikizumab substantially reduced Body Surface Area (BSA) to < 1% (RR: 34.53, p < 0.001) and improved PASI scores (PASI 100 RR: 25.94, PASI 90 RR: 11.50, PASI 75 RR: 10.47, all p < 0.001). Static Physician's Global Assessment (sPGA) scores of 0/1 were achieved (RR: 12.48, p < 0.001). Quality of life measures also improved significantly, with increases in SF-36 Physical and Mental Component Summaries (MD: 4.02 and 3.53 respectively, p < 0.01) and Dermatology Life Quality Index (DLQI) scores of 0/1 (RD: 0.51, p < 0.00001). Importantly, the safety profile of mirikizumab was comparable to the control, with no significant differences in the overall incidence of adverse effects (RR: 0.97; 95% CI: 0.86-1.10) or in serious adverse effects (RR: 1.61; 95% CI: 0.55-4.73). These results collectively demonstrate the efficacy and safety of mirikizumab in treating psoriasis, with significant improvements across multiple clinical and quality-of-life measures. Conclusion This meta-analysis demonstrates that mirikizumab significantly reduces psoriasis severity and improves quality of life, with a favourable safety profile. These findings support its use as a valuable treatment option for moderate-to-severe plaque psoriasis. Further research is needed to assess long-term outcomes and comparative effectiveness.
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