Drug Survival of Interleukin (IL)-17 and IL-23 Inhibitors for the Treatment of Psoriasis: A Retrospective Multi-country, Multicentric Cohort Study


Por: Torres, T, Puig, L, Vender, R, Yeung, J, Carrascosa, JM, Piaserico, S, Gisondi, P, Lynde, C, Ferreira, P, Bastos, PM, Dauden, E, Leite, L, Valerio, J, del Alcazar-Viladomiu, E, Rull, EV, Llamas-Velasco, M, Pirro, F, Messina, F, Bruni, M, Licata, G, Ricceri, F, Nidegger, A, Hugo, J, Mufti, A, Daponte, AI, Teixeira, L, Balato, A, Romanelli, M, Prignano, F, Gkalpakiotis, S, Conrad, C, Lazaridou, E, Rompoti, N, Papoutsaki, M, Nogueira, M, Chiricozzi, A

Publicada: 1 nov 2022 Ahead of Print: 1 ago 2022
Resumen:
Background Drug survival, defined as the length of time from initiation to discontinuation of a given therapy, allows comparisons between drugs, helps to predict patient's likelihood of remaining on a specific treatment, and achieving the best decision for each patient in daily clinical practice. Objective The aim of this study was to provide data on drug survival of secukinumab, ixekizumab, brodalumab, guselkumab, tildrakizumab, and risankizumab in a large international cohort, and to identify clinical predictors that might have an impact on the drug survival of these drugs. Methods This was a retrospective, multicentric, multi-country study that provides data of adult patients with moderate to severe psoriasis who started treatment with an interleukin (IL)-17 or IL-23 inhibitor between 1 February 2015 and 31 October 2021. Data were collected from 19 distinct hospital and non-hospital-based dermatology centers from Canada, Czech Republic, Italy, Greece, Portugal, Spain, and Switzerland. Kaplan-Meier estimator and proportional hazard Cox regression models were used for drug survival analysis. Results A total of 4866 treatment courses (4178 patients)-overall time of exposure of 9500 patient-years-were included in this study, with 3164 corresponding to an IL-17 inhibitor (secukinumab, ixekizumab, brodalumab) and 1702 corresponding to an IL-23 inhibitor (guselkumab, risankizumab, tildrakizumab). IL-23 inhibitors had the highest drug survival rates during the entire study period. After 24 months of treatment, the cumulative probabilities of drug survival were 0.92 (95% confidence interval [CI] 0.89-0.95) for risankizumab, 0.90 (95% CI 0.88-0.92) for guselkumab, 0.80 (95% CI 0.76-0.84) for brodalumab, 0.79 (95% CI 0.76-0.82) for ixekizumab, and 0.75 (95% CI 0.73-0.77) for secukinumab. At 36 months, only guselkumab [0.88 (95% CI 0.85-0.91)], ixekizumab [0.73 (95% CI 0.70-0.76)], and secukinumab [0.67 (95% CI 0.65-0.70)] had more than 40 patients at risk of drug discontinuation. Only two drugs had more than 40 patients at risk of drug discontinuation at 48 months, with ixekizumab demonstrating to have a higher cumulative probability of drug survival [0.71 (95% CI 0.68-0.75)] when compared with secukinumab [0.63 (95% CI 0.60-0.66)]. Secondary failure was the main cause for drug discontinuation. According to the final multivariable model, patients receiving risankizumab, guselkumab, and ixekizumab were significantly less likely to discontinue treatment than those receiving secukinumab. Previous exposure to biologic agents, absent family history of psoriasis, higher baseline body mass index (BMI), and higher baseline Psoriasis Area and Severity Index (PASI) were identified as predictors of drug discontinuation. Conclusion The cumulative probability of drug survival of both IL-17 and IL-23 inhibitors was higher than 75% at 24 months, with risankizumab and guselkumab demonstrating to have overall cumulative probabilities >= 90%. Biological agent chosen, prior exposure to biologic agents, higher baseline BMI and PASI values, and absence of family history of psoriasis were identified as predictors for drug discontinuation. Risankizumab, guselkumab, and ixekizumab were less likely to be discontinued than secukinumab.

Filiaciones:
Torres, T:
 Ctr Hosp Univ Porto, Dept Dermatol, Porto, Portugal

 Univ Porto, Inst Ciencias Biomed Abel Salazar, Porto, Portugal

Puig, L:
 Hosp Santa Creu & Sant Pau, Dept Dermatol, Barcelona, Spain

Vender, R:
 McMaster Univ, Hamilton, ON, Canada

Yeung, J:
 Univ Toronto, Dept Med, Div Dermatol, Prob Med Res, Waterloo, ON, Canada

Carrascosa, JM:
 Autonomous Univ Barcelona UAB, Germans Trias & Pujol Univ Hosp HUGTP, Dept Dermatol, Badalona, Spain

Piaserico, S:
 Univ Padua, Dept Med, Dermatol Unit, I-35128 Padua, Italy

Gisondi, P:
 Univ Verona, Dept Med, Sect Dermatol & Venereol, Verona, Italy

Lynde, C:
 Univ Toronto, Lynde Inst Dermatol, Dept Med, Toronto, ON, Canada

Ferreira, P:
 Hosp CUF Descobertas, Lisbon, Portugal

Bastos, PM:
 Hosp CUF Descobertas, Lisbon, Portugal

Dauden, E:
 Hosp Univ La Princesa, Inst Invest Sanitaria La Princesa IIS IP, Dermatol Dept, Madrid, Spain

Leite, L:
 Clin Med Belem, Lisbon, Portugal

Valerio, J:
 Clin Med Belem, Lisbon, Portugal

del Alcazar-Viladomiu, E:
 Autonomous Univ Barcelona UAB, Germans Trias & Pujol Univ Hosp HUGTP, Dept Dermatol, Badalona, Spain

Rull, EV:
 Hosp Santa Creu & Sant Pau, Dept Dermatol, Barcelona, Spain

Llamas-Velasco, M:
 Hosp Univ La Princesa, Inst Invest Sanitaria La Princesa IIS IP, Dermatol Dept, Madrid, Spain

Pirro, F:
 Univ Cattolica Sacro Cuore, Dipartimento Med & Chirurg Traslaz, Dermatol, Rome, Italy

 Fdn Policlin Univ A Gemelli IRCCS, Dipartimento Sci Med & Chirurg, UOC Dermatol, Rome, Italy

Messina, F:
 Univ Padua, Dept Med, Dermatol Unit, I-35128 Padua, Italy

Bruni, M:
 Univ Verona, Dept Med, Sect Dermatol & Venereol, Verona, Italy

Licata, G:
 Univ Brescia, Dermatol Dept, ASST Spedali Civili Brescia, Brescia, Italy

Ricceri, F:
 Univ Florence, Dept Dermatol Sci, Sect Dermatol, Florence, Italy

Nidegger, A:
 Lausanne Univ Hosp CHUV, Dept Dermatol, Lausanne, Switzerland

 Univ Lausanne, Lausanne, Switzerland

Hugo, J:
 Charles Univ Prague, Fac Med 3, Dept Dermatovenereol, Prague, Czech Republic

 Kralovske Vinohrady Univ Hosp, Prague, Czech Republic

Mufti, A:
 Univ Toronto, Dept Med, Div Dermatol, Prob Med Res, Waterloo, ON, Canada

Daponte, AI:
 Aristotle Univ Thessaloniki, Dept Dermatol Venereol 2, Sch Med, Thessaloniki, Greece

Teixeira, L:
 Univ Porto ICBASUP, Ctr Hlth Technol & Serv Res CINTESIS, Inst Biomed Sci Abel Salazar, Porto, Portugal

Balato, A:
 Univ Campania Luigi Vanvitelli, Unit Dermatol, Naples, Italy

Romanelli, M:
 Univ Pisa, Dept Dermatol, Pisa, Italy

Prignano, F:
 Univ Florence, Dept Dermatol Sci, Sect Dermatol, Florence, Italy

Gkalpakiotis, S:
 Charles Univ Prague, Fac Med 3, Dept Dermatovenereol, Prague, Czech Republic

 Kralovske Vinohrady Univ Hosp, Prague, Czech Republic

Conrad, C:
 Lausanne Univ Hosp CHUV, Dept Dermatol, Lausanne, Switzerland

 Univ Lausanne, Lausanne, Switzerland

Lazaridou, E:
 Aristotle Univ Thessaloniki, Dept Dermatol Venereol 2, Sch Med, Thessaloniki, Greece

Rompoti, N:
 Natl & Kapodistrian Univ Athens, A Sygros Hosp Skin & Venereal Dis, Fac Med, Dept Dermatol Venereol 1, Athens, Greece

Papoutsaki, M:
 Natl & Kapodistrian Univ Athens, A Sygros Hosp Skin & Venereal Dis, Fac Med, Dept Dermatol Venereol 1, Athens, Greece

Nogueira, M:
 Ctr Hosp Univ Porto, Dept Dermatol, Porto, Portugal

Chiricozzi, A:
 Univ Cattolica Sacro Cuore, Dipartimento Med & Chirurg Traslaz, Dermatol, Rome, Italy

 Fdn Policlin Univ A Gemelli IRCCS, Dipartimento Sci Med & Chirurg, UOC Dermatol, Rome, Italy
ISSN: 11750561
Editorial
ADIS INT LTD, 5 THE WAREHOUSE WAY, NORTHCOTE 0627, AUCKLAND, NEW ZEALAND, Nueva Zelanda
Tipo de documento: Article
Volumen: 23 Número: 6
Páginas: 891-904
WOS Id: 000842593900001
ID de PubMed: 35976568
imagen Green Published, Green

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