cost-effective therapeutic based on at-approval cost estimates as the study was conducted at the end of 2016 and brodalumab was approved in February 2017. However, an update of the ICER calculations by Hendrix et al in May 2017 based on the updated wholesale acquisition costs estimated brodalumab to be the most cost-effective therapeutic.5,40
Feldman et al created an economic model in 2018 to assess the impact of brodalumab on pharmacy budget of US commercial healthcare plans.41 Prior to brodalumab approval, the total annual pharmacy budget for biologics was estimated at $414,362,647. With the introduction of brodalumab where usage comprised 3% to 30% of moderate-to-severe psoriasis patients, they estimated a reduction of the total annual pharmacy cost to be between $3,698,129 and $36,981,290.
CONCLUSION
Brodalumab, the first-in-class IL-17 receptor inhibitor, is a safe and effective therapeutic for moderate-to-severe plaque psoriasis. Despite no head-to-head comparisons, brodalumab appears to exhibit faster efficacy compared to IL-17A inhibitors. Brodalumab also has demonstrated efficacy in circumstances where patients have failed IL-17A inhibitors and were switched to brodalumab. In addition, brodalumab has been successful for difficult-to-treat areas such as the nails, scalp, palms, and soles. The latest 4-year pharmacovigilance analytics also reveal no new suicide behavior signals attesting to very low risk of use in a population whose quality of life is so significantly affected by widespread psoriasis. Furthermore, economic analysis of brodalumab usage suggests its utility in lowering healthcare costs in the US given its cost-effectiveness. Thus, brodalumab is an excellent addition to the psoriasis toolkit.
DISCLOSURES
Leon Kircik MD has served as either a speaker, consultant, advisor or an investigator for Abbott Laboratories, Abbvie, Allergan, Inc., Almirall, Amgen, Inc., Arcutis, Biogen-Idec, BMS, Boehringer-Ingleheim, Breckinridge Pharma, Celgene, Centocor, Inc., Cellceutix, Cipher, Combinatrix, Connetics Corporation, Coria, Dermavant, Dermira, Dow Pharmaceutical Sciences, Inc., Dr. Reddy’s Lab, Eli Lilly, Galderma, Genentech, Inc., GlaxoSmithKline PLC, Idera, Johnson & Johnson, Leo, Maruho, Medicis Pharmaceutical Corp., Merck, Nimbus, Novartis AG, Ortho Dermatologics, PharmaDerm, Pfizer, Promius, Serono (Merck Serono International SA), Stiefel Laboratories, Inc., Sun Pharma, Taro, UCB, Valeant Pharmaceuticals Intl, Ventyx, and XenoPort.
REFERENCES
- Vanderpuye-Orgle J, Zhao Y, Lu J, et al. Evaluating the economic burden of psoriasis in the United States. J Am Acad Dermatol. Jun 2015;72(6):961-7.e5. doi:10.1016/j.jaad.2015.02.1099
- Ghoreschi K, Balato A, Enerbäck C, et al. Therapeutics targeting the IL-23 and IL-17 pathway in psoriasis. Lancet. 2021;397(10275):754-766. doi:10.1016/s0140-6736(21)00184-7
- Papp KA, Leonardi C, Menter A, et al. Brodalumab, an anti-interleukin-17-receptor antibody for psoriasis. N Engl J Med. 2012;366(13):1181-9. doi:10.1056/NEJMoa1109017
- Elewski B, Rich P, Lain E, et al. Efficacy of brodalumab in the treatment of scalp and nail psoriasis: results from three phase 3 trials. J Dermatolog Treat. 2022;33(1):261-265. doi:10.1080/0954 6634.2020.1749546
- Hendrix N, Ollendorf DA, Chapman RH, et al. Cost-effectiveness of targeted pharmacotherapy for moderate to severe plaque psoriasis. J Manag Care Spec Pharm. Dec 2018;24(12):1210-1217. doi:10.18553/jmcp.2018.24.12.1210
- Krueger JG, Fretzin S, Suárez-Fariñas M, et al. IL-17A is essential for cell activation and inflammatory gene circuits in subjects with psoriasis. J Allergy Clin Immunol. Jul 2012;130(1):145-54. e9. doi:10.1016/j.jaci.2012.04.024
- Bugaut H, Aractingi S. Major role of the IL17/23 axis in psoriasis supports the development of new targeted therapies. Front Immunol. 2021;12:621956. doi:10.3389/fimmu.2021.621956
- Bianchi E, Rogge L. The IL-23/IL-17 pathway in human chronic inflammatory diseases - new insight from genetics and targeted therapies. Microbes Infect. 2019;21(5-6):246-253. doi:10.1016/j. micinf.2019.06.009
- Johansen C, Usher PA, Kjellerup RB, et al. Characterization of the interleukin-17 isoforms and receptors in lesional psoriatic skin. Br J Dermatol. 2009;160(2):319-24. doi:10.1111/j.1365-2133.2008.08902.x
- Nies JF, Panzer U. IL-17C/IL-17RE: Emergence of a unique axis in T(H)17 biology. Front Immunol. 2020;11:341. doi:10.3389/fimmu.2020.00341
- Simopoulou T, Tsiogkas SG, Zafiriou E, et al Secukinumab, ixekizumab, bimekizumab and brodalumab for psoriasis and psoriatic arthritis. Drugs Today (Barc). 2023;59(3):135-167. doi:10.1358/dot.2023.59.3.3419557
- Frieder J, Kivelevitch D, Menter A. Secukinumab: a review of the anti-IL-17A biologic for the treatment of psoriasis. Ther Adv Chronic Dis. 2018;9(1):5-21. doi:10.1177/2040622317738910
- Shelton SK, Bai SR, Jordan JK, et al. Ixekizumab: a review of its use for the management of moderate to severe plaque psoriasis. Ann Pharmacother. Mar 2019;53(3):276-284. doi:10.1177/1060028018799982
- Papp KA, Reich K, Paul C, et al. A prospective phase III, randomized, double-blind, placebo-controlled study of brodalumab in patients with moderate-to-severe plaque psoriasis. Br J Dermatol. 2016;175(2):273-86. doi:10.1111/bjd.14493
- Langley RG, Elewski BE, Lebwohl M, et al. Secukinumab in plaque psoriasis--results of two phase 3 trials. N Engl J Med. 014;371(4):326-38. doi:10.1056/NEJMoa1314258
- Gordon KB, Blauvelt A, Papp KA, et al. Phase 3 trials of ixekizumab in moderate-to-severe plaque psoriasis. N Engl J Med. Jul 28 2016;375(4):345-56. doi:10.1056/NEJMoa1512711
- Lebwohl M, Strober B, Menter A, et al. Phase 3 studies comparing brodalumab with ustekinumab in psoriasis. N Engl J Med. 2015;373(14):1318-28. doi:10.1056/NEJMoa1503824
- Blauvelt A, Reich K, Tsai TF, et al. Secukinumab is superior to ustekinumab in clearing skin of subjects with moderate-to-severe plaque psoriasis up to 1 year: Results from the CLEAR study. 2017;76(1):60-69.e9. doi:10.1016/j. jaad.2016.08.008
- Bissonnette R, Luger T, Thaçi D, et al. Secukinumab demonstrates high sustained efficacy and a favourable safety profile in patients with moderate-to-severe psoriasis through 5 years of treatment (SCULPTURE Extension Study). J Eur Acad Dermatol Venereol. 2018;32(9):1507-1514. doi:10.1111/jdv.14878
- Leonardi C, Reich K, Foley P, et al. Efficacy and safety of ixekizumab through 5 years in moderate-to-severe psoriasis: long-term results from the UNCOVER-1 and UNCOVER-2 Phase-3 randomized controlled trials. Dermatol Ther (Heidelb). Jun 2020;10(3):431-447. doi:10.1007/s13555-020-00367-x
- Lebwohl MG, Blauvelt A, Menter A, et al. Efficacy, safety, and patient-reported outcomes in patients with moderate-to-severe plaque psoriasis treated with brodalumab for 5 years in a long-term, open-label, phase II study. Am J Clin Dermatol. Dec 2019;20(6):863-871. doi:10.1007/s40257-019-00466-2
- Fried R, Lebwohl M, Bettencourt M, et al. Onset of plaque psoriasis treatment responses with anti-IL-17/IL-23 biologic therapies. J Drugs Dermatol. Aug 1 2022;21(8):854-860. doi:10.36849/jdd.66791
- Bewley A, Burrage DM, Ersser SJ, et al. Identifying individual psychosocial and adherence support needs in patients with psoriasis: a multinational two-stage qualitative and quantitative study. J Eur Acad Dermatol Venereol. 2014;28(6):763-70. doi:10.1111/jdv.12174
- Lebwohl M, Cather J, Armstrong A, et al. Recapture rate of brodalumab in patients with a lapse in treatment. J Drugs Dermatol. 2020;19(4):384-387. doi:10.36849/jdd.2020.5026
- Blauvelt A, Reich K, Warren RB, et al. Secukinumab re-initiation achieves regain of high response levels in patients who interrupt treatment for moderate to severe plaque psoriasis. Br J Dermatol. 2017;177(3):879-881. doi:10.1111/bjd.15656
- Blauvelt A, Papp KA, Sofen H, et al. Continuous dosing versus interrupted therapy with ixekizumab: an integrated analysis of two phase 3 trials in psoriasis. J Eur Acad Dermatol Venereol. 2017;31(6):1004-1013. doi:10.1111/jdv.14163
- Langley RG, Armstrong AW, Lebwohl MG, et al. Efficacy and safety of brodalumab in patients with psoriasis who had inadequate responses to ustekinumab: subgroup analysis of two randomized phase III trials. Br J Dermatol. Feb 2019;180(2):306 314. doi:10.1111/bjd.17318
- Gasslitter I, Kirsten N, Augustin M, et al. Successful intra-class switching among IL-17 antagonists: a multicentre, multinational, retrospective study. Arch Dermatol Res. Jul 2019;311(5):421-424.doi:10.1007/s00403-019-01907-y
- Kimmel G, Chima M, Kim HJ, et al. Brodalumab in the treatment of moderate to severe psoriasis in patients when previous anti-interleukin 17A therapies have failed. J Am Acad Dermatol. 2019;81(3):857-859. doi:10.1016/j.jaad.2019.05.007
- Kromer C, Wilsmann-Theis D, Gerdes S, et al. Changing within the same class: efficacy of brodalumab in plaque psoriasis after treatment with an IL-17A blocker - a retrospective multicenter study. J Dermatolog Treat. 2021;32(8):878-882. doi:10.1080/095 46634.2020.1716932
- Yeung J, Vender R, Turchin I, et al. Brodalumab success in patients with moderate-to-severe psoriasis who failed previous interleukin-17A inhibitors. J Am Acad Dermatol. 2021;84(4):1169-1171. doi:10.1016/j.jaad.2020.11.013
- Gregoriou S, Tsiogka A, Tsimpidakis A, et al. Treatment of nail psoriasis with brodalumab: an open-label unblinded study. J Eur Acad Dermatol Venereol. 2021;35(4):e299-e301. doi:10.1111/jdv.17055
- Pinter A, Bonnekoh B, Hadshiew IM, et al. Brodalumab for the treatment of moderate-to-severe psoriasis: case series and literature review. Clin Cosmet Investig Dermatol. 2019;12:509-517.doi:10.2147/ccid.S211938
- Nakagawa H, Niiro H, Ootaki K. Brodalumab, a human anti-interleukin-17-receptor antibody in the treatment of Japanese patients with moderate-to-severe plaque psoriasis: Efficacy and safety results from a phase II randomized controlled study. J Dermatol Sci. 2016;81(1):44-52. doi:10.1016/j. jdermsci.2015.10.009
- Politou M, Pompou M, Afroditi KI, et al. 18501 Twenty patients with moderate to severe psoriasis successfully treated with brodalumab after a failed treatment with secukinumab. Journal of the American Academy of Dermatology. 2020;83(6):AB214. doi:10.1016/j.jaad.2020.06.946
- Siliq [package insert]. Bridgewater, NJ: Bausch Health US, LLC; 2020.
- Papp K, Menter A, Leonardi C, et al. Long-term efficacy and safety of brodalumab in psoriasis through 120 weeks and after withdrawal and retreatment: subgroup analysis of a randomized phase III trial (AMAGINE-1). Br J Dermatol. 2020;183(6):1037-1048. doi:10.1111/bjd.19132
- Lebwohl M, Koo J, Leonardi C, et al. Brodalumab: 4-Year US pharmacovigilance report. J Drugs Dermatol. 2023;22(4):419-422. doi:10.36849/jdd.7344
- Brixner D, Oderda G, Biskupiak J, et al. The challenge of variable costs in decisions based on cost-effectiveness evidence: a case study for brodalumab. Am Health Drug Benefits. 2019;12(1):22-26.
- Wu JJ, Feldman SR, Rastogi S, et al Comparison of the cost-effectiveness of biologic drugs used for moderate-to-severe psoriasis treatment in the United States. J Dermatolog Treat. 2018;29(8):769-774. doi:10.1080/09546634.2018.1466022
- Feldman SR, Wu JJ, Rastogi S, et al The budget impact of brodalumab for the treatment of moderate-to-severe plaque psoriasis on US commercial health plans. J Med Econ. 2018;21(5):537-541. doi:10.1080/13696998.2018.1431920
AUTHOR CORRESPONDENCE
Leon Kircik MD wedoderm@yahoo.com