Matching-Adjusted Indirect Comparison of Ravulizumab/Efgartigimod in Generalized Myasthenia Gravis: Timepoint Challenges


Topic:

Clinical Trials

Poster Number: M267

Author(s):

Sven Meuth, MD, University of Munster, Munster, Germany, Tim Hagenacker, MD, University Hospital Essen, Essen, Germany, Christopher Scheiner, MD, PhD, University of Tennessee, Knoxville, TN, USA, Masayuki Masuda, MD, Tokyo Medical University, Tokyo, Japan, Adrian Kielhorn, MBA, Alexion, AstraZeneca Rare Disease, Boston, MA, USA, Brian Werneburg, PhD, Alexion, AstraZeneca Rare Disease, Boston, MA, USA, Lauren Powell, MPH, Broadstreet Health Economics & Outcomes Research, Vancouver, BC, Canada, Basia Rogula, MSc, Broadstreet Health Economics & Outcomes Research, Vancouver, BC, Canada, Karissa Johnston, MSc, PhD, Broadstreet Health Economics & Outcomes Research, Vancouver, BC, Canada

Background: Matching-adjusted indirect comparisons (MAICs) can assess treatment benefits for symptom control in patients with generalized myasthenia gravis (gMG).
Objective: Building on previous comparisons of ravulizumab and efgartigimod, we performed a MAIC using mean changes from baseline in Myasthenia Gravis Activities of Daily Living (MG-ADL) scores from the CHAMPION-MG and ADAPT trials to assess the effects of these treatments on symptom control at different timepoints in patients with gMG.
Methods: Individual patient-level data from CHAMPION-MG were weighted to match summary baseline characteristics from the acetylcholine receptor antibody–positive subset of patients in ADAPT at the trial-arm level. Mean changes in MG-ADL scores from baseline to different timepoints were compared, and anchored comparisons were performed at weeks 4 and 10, and at week 8 (efgartigimod) vs week 26 (ravulizumab).
Results: Patients from CHAMPION-MG (N = 175) and ADAPT (N = 129) were included, with similar baseline characteristics across both studies. Improvements in MG-ADL scores varied across timepoints and appeared to favor efgartigimod vs ravulizumab at week 4 (mean MG-ADL change from baseline, −1.6; 95% confidence interval [CI], −3.0 to −0.3). However, at week 10 (mean change from baseline, 1.0; 95% CI, −0.5 to 2.5), and at week 8 (efgartigimod) vs week 26 (ravulizumab; mean change from baseline, 1.2; 95% CI, −0.2 to 2.7), the results trended in favor of ravulizumab.
Conclusions: Outcomes from indirect comparisons of symptom control in patients with gMG treated with ravulizumab vs efgartigimod can vary depending on timepoints and matching methodology. Consistency of symptom control over a prolonged period should be considered, alongside efficacy and tolerability, when assessing treatments for gMG.
Previously presented at EAN, 2023. Meuth S, et al. Eur J Neurol. 2023;30(suppl 1):467. Reused with permission.