Eleven biologic drugs are currently approved for
psoriasis management. Real-life studies are needed to guide clinicians in choosing a tailored-tail
therapy. The aim of our retrospective study is to indirectly compare the efficacy and safety of
ixekizumab and
brodalumab in
psoriasis patients. A single-centre real-life retrospective study was performed enrolling moderate-to-severe psoriatic patients under biologic treatment with
ixekizumab or
brodalumab. For each patient, clinical and demographic data were collected and the effectiveness and safety of
brodalumab and
ixekizumab treatment were evaluated at weeks 4, 12, and 24.
Psoriasis Area Severity Index (PASI) and Body Surface Area (BSA) were used for
psoriasis severity. A total of 139 patients were included in the study: 98(70.5%) and 41(29.5%) patients received
ixekizumab and
brodalumab, respectively. Mean PASI and BSA significantly reduced at each follow up for both
ixekizumab and
brodalumab groups. Even if
ixekizumab reached higher rates of PASI90 and PASI100 than
brodalumab (PASI90: 43.8% vs. 39.0% PASI100: 20.4% vs. 17.1% at week4 and PASI90: 83.6% vs. 75.6% PASI100: 71.5% vs. 60.9% at week24), these results were not statistically significant. Adverse events, mainly mild, were registered in 25.5% of
ixekizumab and 26.8% of
brodalumab group, respectively. Discontinuation rate was higher for
brodalumab (17.1% vs. 9.1%), without statistical significance. Our study showed comparable efficacy and safety for
ixekizumab and
brodalumab.