The Risk of Malignancy in Secukinumab-Treated Psoriasis, Psoriatic Arthritis, and Ankylosing Spondylitis Patients The British Journal of Dermatology
TAKE-HOME MESSAGE
The authors report the 5-year safety data from the secukinumab clinical trial program and post-marketing surveillance data of patients with psoriasis, psoriatic arthritis, and ankylosing spondylitis. Malignancy was reported in 204 patients out of 23,908 patient treatment-years. The cumulative exposure–adjusted incidence rate of malignancy was 0.85 per 100 patient-years of treatment. The two most prevalent malignancies were basal cell carcinoma and squamous cell carcinoma. There were no cases of non-Hodgkin's lymphoma. The observed malignancy rate was similar to the expected rate in the general United States population.
- The long-term safety profile for up to 5 years of treatment with secukinumab for psoriasis, psoriatic arthritis, and ankylosing spondylitis is favorable and supports its use for these conditions.
BACKGROUND
Data on the use of biologic therapy and malignancy risk are inconsistent due to limited long-term robust studies.
OBJECTIVE
To assess the malignancy risk in secukinumab-treated psoriasis, psoriatic arthritis (PsA) and ankylosing spondylitis (AS) patients.
METHODS
This integrated safety analysis from both the secukinumab clinical trial program and post-marketing safety surveillance data included any patient receiving at least one approved dose of secukinumab with a maximum of five years follow-up. Safety analyses evaluated the rate of malignancy using exposure-adjusted incidence rates (EAIR; incidence rates/100-patient treatment-years [PTY]). Standardised incidence ratios (SIR) were reported using the Surveillance, Epidemiology, and End Results Program (SEER) database as a reference population. The crude incidence of malignancy was also reported using post-marketing surveillance data.
RESULTS
Safety data from 10,685 psoriasis, 2,523 PsA and 1,311 AS secukinumab-treated patients from 49 clinical trials were included. Across indications over a five-year period, the EAIR of malignancy was 0.85/100 PTY (95% confidence intervals [CI]: 0.74, 0.98) in secukinumab-treated patients, corresponding to 204 patients/23,908 PTY. Overall, the observed vs. expected number of malignancies from secukinumab clinical trial data were comparable, as indicated by a SIR of 0.99 (95% CI: 0.82, 1.19) across indications. The estimated crude cumulative incidence reporting rate/100 PTY for malignancy was 0.27 in the post-marketing surveillance data across indications with a cumulative exposure of 285,811 PTY.
CONCLUSIONS
In this large safety analysis, the risk of malignancy was low for up to five years of secukinumab treatment. These data support the long-term us of secukinumab in these indications.
The Risk of Malignancy in Secukinumab-Treated Psoriasis, Psoriatic Arthritis and Ankylosing Spondylitis Patients: Analysis of Up to Five-Year Clinical Trial and Post-Marketing Surveillance Data
Br J Dermatol 2021 Apr 08;[EPub Ahead of Print], M Lebwohl, A Deodhar, CEM Griffiths, MA Menter, D Poddubnyy, W Bao, V Jehl, K Marfo, P Primatesta, A Shete, V Trivedi, PJ MeaseSkin Care Physicians of Costa Rica
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