Psoriasis is an inflammatory, immune-mediated, systemic, chronic disease.1,2 Epidemiologic studies from around the world have estimated the prevalence of psoriasis to be 0.6%–4.8%.3 In Turkey, a prevalence of 0.7%–1.8% has been reported in clinical studies.4,5

Recently, the use of cytokine-targeted therapies has increased for the treatment of moderate-to-severe psoriasis. Secukinumab is a human monoclonal IgG1 k antibody that was developed to block the actions of IL-17A.6–9 In 2015, an anti-IL-17 was approved for the first time, for the treatment of moderate-to-severe psoriasis and psoriatic arthritis in adult patients.10 Secukinumab has demonstrated high efficacy for the treatment of moderate-to-severe psoriasis and psoriatic arthritis, with a rapid onset of action, sustained response, and favorable safety profile.11,12 Data from the ERASURE and FIXTURE studies revealed that a 300mg subcutaneous (s.c.) dose achieves a peak effect at week 16, with efficacy sustained over 52 weeks of treatment.13 Regarding safety, IL-17A inhibitors are associated with various side effects and an increased incidence of candidal infections.11,13 To date, there is a scarcity of literature on real-world data in terms of the efficacy and safety of secukinumab. In this study, the authors analyzed the efficacy, safety, and side effects of secukinumab in patients with moderate-to-severe psoriasis.

Secukinumab is a biological drug used for the treatment of psoriasis and acts by inhibiting IL-17A.14 Various real-world studies have reported on the efficacy and safety of secukinumab in psoriasis (Table 4). In a recent prospective multicenter study including 158 patients, the proportions of patients achieving PASI 75 at weeks 12, 24, and 52 were found to be 83.5%, 89%, and 78.5%, respectively; the proportions achieving PASI 90 at the same time points were 62%, 64.6%, and 63.2%.15 The authors found PASI 75 and PASI 90 responses of 79.9% and 69.8% at week 24, and 53.2% and 49.3% at week 52, respectively. The proportions achieving PASI 100 at the same points were 52.2% and 58.52%, respectively.

Georgakopoulos et al. suggested that fewer psoriasis patients in real-world clinical practice maintain efficacious outcomes at week 52 than those enrolled in randomized-controlled studies.16 Although PASI 75/90 response decreased gradually over 52-weeks of secukinumab, the PASI 100 response rate was higher in the present study’s cohort.

In another study, 69 patients with psoriasis who started treatment with secukinumab primarily due to failure of anti-TNF and/or anti-IL12-23 treatment were evaluated. At week 12, 66.7% of the patients still on secukinumab had experienced at least a 50% reduction in PASI (PASI 50) from baseline.17 In the present study, 225 (98%) patients were still receiving treatment at week 12 and approximately 50% of them achieved PASI 100.

In Notario et al.’s study, the percentages of patients with a BMI≥30kg/m² who achieved PASI 75 and PASI 90 responses were significantly lower than those with a BMI<30kg/m2.18 In another study, an analysis of all patients receiving 300mg secukinumab for 12 weeks showed that the proportion of PASI 75 responders was lower among those with a BMI>25kg/m2 than in those with a BMI<25kg/m2.19 In contrast, Schwensen et al. reported that baseline PASI scores were not different according to obesity status (and where BMI>25kg/m2 is considered obese).17 Similar to Schwensen et al., the authors did not detect an association between BMI and PASI response.

Galluzzo et al. showed that younger patients responded to treatment more quickly: the rates of PASI 75, PASI 90, and PASI 100 were higher in those patients at week 4. Other parameters, such as sex and the PASI score at baseline, were not associated with the PASI 75, PASI 90, and PASI 100 response rates.20 Similarly, Huang et al. observed that young age was associated with a better clinical response to secukinumab.21 There was a significant association between the PASI response and disease duration in the present study. Shorter disease duration was associated with lower PASI scores at week 24 (p=0.016), but there were no such associations with age or sex. In another study, PASI 75 response was found lower in patients with psoriatic arthritis when compared to patients without psoriatic arthritis.22 Ortiz-Salvador et al. showed that PASI 75 and PASI 90 rates were not associated with the baseline PASI score, age, sex, smoking status, or presence of psoriatic arthritis or dyslipidemia.15 The degree of improvement in the PASI score had no association with psoriatic arthritis in the present study’s cohort, but the mean PASI score was lower in patients without comorbidities at week 12 (p=0.034).

Galluzzo et al. enrolled 107 patients (75% males) with psoriasis, with a mean age of 47.5 years, in their retrospective study. Approximately 51.3% of the patients had comorbidities; the most frequent were obesity (23.4%), hypertension (15%), hyperlipidemia (13.1%), and type 2 diabetes (10.3%).20 Similarly, in the present study, the most frequently observed comorbidities were obesity (31%), hypertension (17.9%), hyperlipidemia (12.23%), and diabetes mellitus (11.35%). Galluzzo et al. also showed that PASI 75, PASI 90, and PASI 100 were achieved more frequently by treatment-naive patients at weeks 12 and 24. In total, 55 (51.4%) patients had previously been treated with other biologic therapies, and 52 (48.6%) were naive to biologics.20 Similarly, in another study, prior exposure to ≥1 biological therapy was associated with a diminished therapeutic response to secukinumab at week 16.18 In Ger’s study, the response rates of PASI 50, and PASI 75 at weeks 12 and 24 in patients without prior biologic failure were also significantly greater than those with prior biologic failure.23 In the present study, while 111 (48.4%) patients were bio-naive, 118 (51.5%) were bio-switched. With respect to the PASI response, there was no significant difference between the bio-naive and bio-switched patients (p>0.5). In another study, no significant difference in efficacy was observed between bio-naive and bio-switched patients.24

Carpentieri et al. divided their secukinumab patients into the bio-naive, history of the inefficacy of one biological agent, and unresponsive to ≥2 biological agent groups. At the end of the study, they reported that PASI scores had declined at 3 and 12-months in all groups.25 The authors also analyzed patients who had received one or more than one biological agents. After treatment, the PASI score had declined in both groups at 12, 24, and 52 weeks.

Carpentieri et al. found that 18 of 120 patients (15%) discontinued secukinumab (8 due to adverse events and 10 due to lack of efficacy).25 Notario et al. reported a discontinuation rate of 21.3% (29/136). The reasons cited for discontinuation included serious adverse events, lack of efficacy, loss of follow-up, pregnancy, and major surgery.18 In another study, the patients who discontinued and pursued treatment received secukinumab for a median of 25.5 and 99.9 weeks, respectively. Out of 91 patients, 22 (24.2%) discontinued secukinumab due to loss of efficacy (14 patients, 15%), adverse events (5 patients, 5.4%), desire for pregnancy (2 patients), and loss to follow-up (1 patient).26 In the study of Ortiz-Salvador et al., 27 (17.1%) patients discontinued treatment due to a lack of efficacy (8 patients), loss of efficacy (15 patients), or loss of follow-up (4 patients).15

In the present study, 155 (68%) patients reached treatment week 52, and 74 (32%) discontinued treatment. Reasons for discontinuation included various adverse events (10.48%), secondary ineffectiveness (8.73%), non-adherence to treatment (5.24%), and patient request (5.24%), among other reasons. The most common adverse events related to discontinuation were fatigue, nasopharyngitis, and candidal infections.

In real-world studies, the adverse events rate for secukinumab ranged from 7.2% to 61%.22,23 Adverse events reported by Zhao et al. included nasopharyngitis, superficial skin bacterial infections, itching, urticaria, and eczema.27 Ortiz-Salvador et al. reported adverse events in 28 patients (17.7%), the most frequent of which were headache (5.7%), nasopharyngitis (5.7%), and hypertension (3.8%).15 In the SIGNATURE study, which investigated the efficacy of secukinumab in patients for whom TNF-α inhibitor therapy had failed, treatment-emergent adverse events occurred in 83.7% of cases; however, most of the events were mild or moderate in severity.28

Recently, the authors analyzed the adverse effects of the biological agents used in the treatment of psoriasis. The rate of adverse effects was 67.4% in patients using anti-TNF-α agents, and 55.3% in those using IL inhibitors (ustekinumab and secukinumab). However, the rates of serious adverse effects were similar (4.8% in the anti-TNF-α group and 3% in the IL inhibitors), (but less frequent in secukinumab [1.6%]).29

In the current study, there were no serious adverse events with secukinumab treatment for up to 52-weeks. The rate of adverse events was 58.9% (135 patients). The most commonly observed adverse effect was candidal infection (10.04%), followed by fatigue (7.42%).

The IL-17 pathway regulates immunity in candida infection, probably via upregulation of proinflammatory cytokines (IL-6 and neutrophil-recruiting chemokines) among other actions, and the use of IL-17 inhibitors have was associated with an increased risk of mucocutaneous candidiasis.30 The rate of candida infection with the use of secukinumab varies between 0.0% and 5.0%.31 In a Japanese study, candida infection was detected in only 1 of 52 patients with psoriasis and completely resolved within 14-days without discontinuation of treatment.32 However, in another study of 91 patients taking secukinumab, the treatment was stopped in 1 patient with oral candidiasis.22 In two other studies, the rates of candida infection were identical (3.7%).15,18

A recent study reported candida infections in 16 patients with psoriasis treated with secukinumab 300mg for 12 months. All patients were evaluated clinically, and swab samples and coculture for candida infection were obtained during therapy. Oral swabs were positive for candida Albicans in two patients and coproculture was positive in one patient. After 12 months of secukinumab therapy, all patients were negative for candida infection, although no antifungal therapy was prescribed, and no patient showed clinical signs of candida infection.33

In another study, candida infection was reported in 5.7% of patients. The most common forms of candidiasis were oral (3.6%), vulvovaginal (0.9%), genital (0.3%), and esophageal (0.6%).34

The authors observed candida infection in 23 patients (10.04%). This high rate may be related to the thoroughness of the examinations, particularly for candida. In most cases, candidiasis was vulvovaginal, intertriginous, or oropharyngeal. Topical treatment was sufficient for most patients; systemic therapy was used in only five patients. Four of those patients (1.75%) discontinued secukinumab treatment due to candidal infection; most had mucosal involvement.

Paradoxical reactions, such as palmoplantar psoriasis and inverse psoriasis, have been described in the literature in association with anti-TNF-α inhibitors, secukinumab, and ustekinumab. Paradoxical arthritis may be triggered by ustekinumab, but has rarely been reported in association with secukinumab.24,35 Interestingly, paradoxical arthritis developed in 13 of the patients (5.68%) with psoriasis. The authors suspect that arthritis occurred as a result of changes in cytokine balance and previously used biological agents.

The limitations of this study include its retrospective design, which caused some difficulties with respect to data access. In addition, due to the small number of patients in some groups, analysis of minor differences was not possible.

In this study, the PASI 90 and PASI 100 response rates were high in patients with moderate-to-severe psoriasis. Unlike other studies, the authors found that PASI scores declined more rapidly in patients with a short disease duration at 24-weeks, and lower mean PASI scores were achieved in patients without comorbidities at 12-weeks. These results show that factors such as the presence of comorbidities and disease duration can affect PASI responses in a negative way. As in other studies, adverse events such as fatigue and nasopharyngitis occurred in the studied cohort. However, the rates of candidal infection and paradoxical arthritis were higher in the present patient population compared to other real-world studies.

None declared.

Ilteris Oguz Topal: Study conception and planning, preparation and writing of the manuscript, final approval of the final version of the manuscript.

Sevim Baysak: Data collection and/or processing, investigation.

Ilknur Kıvanc Altunay: Manuscript critical review, writing of the manuscript, analysis and data interpretation.

Asude Kara Polat: Data collection and/or processing, methodology.

Eylem Emel Arıkan: Data collection and/or processing.

Ezgi Özkur: Data collection and/or processing, literature review.

Sema Aytekin: Data collection and/or processing, literature review.

Bilal Dogan: Data collection and/or processing.

Tuğba Özkök Akbulut: Data collection and curation.

Filiz Topaloğlu Demir: Data collection and curation.

Ayse Serap Karadağ: Manuscript critical review, data collection.

None declared.