Long-term health-related quality of life in patients treated with subcutaneous C1-inhibitor
replacement therapy for the prevention of hereditary angioedema attacks: findings
from the COMPACT open-label extension study
Lumry, William R. ✉; Zuraw, Bruce; Cicardi, Marco; Craig, Timothy; Anderson, John; Banerji, Aleena; Bernstein, Jonathan A.; Caballero, Teresa; Farkas, Henriette [Farkas, Henriette (klinikai immunoló...), author] III. Department
of Internal Medicine (SU / FM / C); Gower, Richard G.; Keith, Paul K.; Levy, Donald S.; Li, H. Henry; Magerl, Markus; Manning, Michael; Riedl, Marc A.; Lawo, John-Philip; Prusty, Subhransu; Machnig, Thomas; Longhurst, Hilary; COMPACT Investigators [Collaborative Organization]
Background: Long-term prophylaxis with subcutaneous C1-inhibitor (C1-INH[SC]; HAEGARDA,
CSL Behring) in patients with hereditary angioedema (HAE) due to C1-INH deficiency
(C1-INH-HAE) was evaluated in an open-label extension follow-up study to the international,
double-blind, placebo-controlled COMPACT study. The current analysis evaluated patient-reported
health-related quality of life (HRQoL) data from 126 patients in the open-label extension
study randomized to treatment with C1-INH(SC) 40 IU/kg (n = 63) or 60 IU/kg (n = 63)
twice weekly for 52 weeks. HRQoL was evaluated at the beginning of the open-label
study and at various time points using the European Quality of Life-5 Dimensions Questionnaire
(EQ-5D), the Hospital Anxiety and Depression Scale (HADS), the Work Productivity and
Activity Impairment Questionnaire (WPAI), and the Treatment Satisfaction Questionnaire
for Medication. The disease-specific Angioedema Quality of Life Questionnaire (AE-QoL)
and HAE quality of life questionnaire (HAE-QoL) instruments were administered in a
subset of patients. Statistical significance was determined by change-from-baseline
95% confidence intervals (CIs) excluding zero. No adjustment for multiplicity was
done. Results: Mean baseline EQ-5D scores (Health State Value, 0.90; Visual Analog
Scale, 81.32) were slightly higher (better) than United States population norms (0.825,
80.0, respectively) and mean HADS anxiety (5.48) and depression (2.88) scores were
within "normal" range (0-7). Yet, patients using C1-INH(SC) 60 IU/kg demonstrated
significant improvement from baseline to end-of-study on the EQ-5D Health State Value
(mean change [95% CI], 0.07 [0.01, 0.12] and Visual Analog Scale (7.45 [3.29, 11.62]).
In the C1-INH(SC) 60 IU/kg group, there were significant improvements in the HADS
anxiety scale (mean change [95% CI], - 1.23 [- 2.08, - 0.38]), HADS depression scale
(- 0.95 [- 1.57, - 0.34]), and WPAI-assessed presenteeism (mean change [95% CI], -
23.33% [- 34.86, - 11.81]), work productivity loss (- 26.68% [- 39.92, - 13.44]),
and activity impairment (- 16.14% [- 26.36, - 5.91]). Clinically important improvements
were achieved in >= 25% of patients for all domains except WPAI-assessed absenteeism
(which was very low at baseline). Mean AE-QoL total score by visit ranged from 13.39
to 17.89 (scale 0-100; lower scores = less impairment). Mean HAE-QoL global scores
at each visit (115.7-122.3) were close to the maximum (best) possible score of 135.
Conclusions Long-term C1-INH(SC) replacement therapy in patients with C1-INH-HAE leads
to significant and sustained improvements in multiple measures of HRQoL.