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Rapid improvements in health-related quality of life and itch with ixekizumab treatment in randomized phase 3 trials: results from UNCOVER-2 and UNCOVER-3

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Published:1st Sep 2017

Author: Leonardi CL, Blauvelt A, Sofen HL, Gooderham M, Augustin M, Burge R, et al.

Source: Journal of the European Academy of Dermatology and Venereology

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Ref.:J Eur Acad Dermatol Venereol. 2017 Sep;31(9):1483-1490.

DOI:10.1111/jdv.14211

Rapid improvements in health-related quality of life and itch with ixekizumab treatment in randomized phase 3 trials: results from UNCOVER-2 and UNCOVER-3

Background: Patients with moderate-to-severe psoriasis report impaired health-related quality of life (HRQoL).

Objective: To assess speed of onset of ixekizumab-induced clinically relevant improvement in HRQoL.

Methods: This post-hoc analysis used pooled data from patients randomized in UNCOVER-2 and UNCOVER-3, and treated with 80 mg ixekizumab every 2 weeks (IXEQ2W), 80 mg ixekizumab every 4 weeks (IXEQ4W), 50 mg etanercept (ETN) twice weekly, or placebo (PBO) for 12 weeks. HRQoL and pruritus were assessed using the Dermatology Life Quality Index (DLQI) and Itch Numeric Rating Scale (NRS), respectively. Minimally clinical important differences (MCID) in DLQI and Itch NRS were defined as ≥ 5-point and ≥ 4-point improvements from baseline, respectively. Time to response from randomization was estimated using Kaplan-Meier methodology and the log-rank test. Hazard ratios between treatments were calculated using a Cox proportional hazards regression model adjusting for studies.

Results: A total of 2570 patients were included: 361 PBO; 740 ETN; 733 IXEQ4W; and 736 IXEQ2W. Significantly greater differences in time to DLQI ≥5 point or Itch NRS ≥4 point improvement for IXEQ2W or IXEQ4W compared to ETN and PBO (P<.001) were observed. The median time when 50% of patients reached a ≥ 5-point reduction in DLQI was shorter for ixekizumab-treated patients (2 weeks, both schedules) compared to ETN- (4 weeks) or PBO-treated (> 12 weeks) patients. Likewise, the median time when 50% of patients reached a ≥ 4-point reduction in Itch NRS was significantly shorter for ixekizumab-treated patients (2 weeks, both schedules) compared to ETN- (8 weeks) or PBO-treated (> 12 weeks) patients. Significantly more ixekizumab-treated patients were likely to achieve MCIDs in DLQI or itch reduction compared to ETN or PBO after 12 weeks of treatment.

Conclusion: Ixekizumab-treated patients achieved more rapid improvements both in HRQoL and itch compared to patients treated with ETN and PBO.

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