Premium
Comparison of analysis approaches for phase III clinical trials in amyotrophic lateral sclerosis
Author(s) -
Healy Brian C.,
Schoenfeld David
Publication year - 2012
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.23392
Subject(s) - amyotrophic lateral sclerosis , clinical trial , survival analysis , rating scale , physical medicine and rehabilitation , medicine , physical therapy , statistics , mathematics , disease
In this study we explore several methods for incorporating survival information in the analysis of Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS) scores. Methods: ALSFRS scores and patient survival times were simulated based on estimates from a recent clinical trial. Six analysis approaches were applied to the data. Each approach was based on ALSFRS scores, the survival time, or a combination of the 2. The power of each approach to detect potential treatment effects was estimated. Results: When the treatment acted solely on the change in ALSFRS, the shared parameter model provided the most power, although all of the models based on random effects were similar. As the effect on survival increased, rank‐based analysis showed potential gains in power. Survival analysis was superior under a small effect on ALSFRS and a larger effect on mortality. Conclusions: The shared parameter model and rank‐based approach can offer improvements in power over traditional approaches. Muscle Nerve 46: 501–511, 2012