4.6 Article

Clinical staging in amyotrophic lateral sclerosis: analysis of Edaravone Study 19

Journal

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
Volume 92, Issue 2, Pages 165-171

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jnnp-2020-323271

Keywords

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Funding

  1. Mitsubishi Tanabe Pharma America, Inc. (MTPA)
  2. MTPA
  3. EU Joint Programme -Neurodegenerative Disease Research (JPND) project
  4. JPND, UK
  5. Medical Research Council [MR/L501529/1, MR/R024804/1]
  6. Economic and Social Research Council [ES/L008238/1]
  7. Motor Neurone Disease Association
  8. National Institute for Health Research Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
  9. Italian Ministry of Education, University and Research
  10. MRC [MR/R024804/1] Funding Source: UKRI

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This study analyzed data from the Edaravone Phase III Study 19 and found that the King's and MiToS staging systems are useful in assessing clinical progression in ALS. Edaravone treatment showed lower progression rates in King's stage compared to placebo, while the opposite was observed in MiToS stage.
Objective This was a post hoc analysis of the Edaravone Phase III Study MCI186-19 ('Study 19') to examine the utility of clinical staging systems as end points in clinical trials in amyotrophic lateral sclerosis (ALS). Methods Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised item scores from Study 19 were retrospectively mapped to King's stage and Milano-Torino staging (MiToS) stage. We assessed the percentage of patients who experienced progression in King's and MiToS stages during Study 19. We also assessed disease progression in subgroups of patients according to baseline King's stage. Results During double-blind treatment, the percentage of patients who experienced a progression in King's stage was lower for edaravone (42.0%, 95% CI 30.4% to 53.6%) than placebo (55.9%, 95% CI 44.1% to 67.6%). The most pronounced effect was noted among patients who were in stage 1 and was maintained throughout open-label treatment. An analysis of a >= 2-stage progression in MiToS stage showed no difference between treatment arms during double-blind treatment, but during the open-label period, more rapid progression was noted among patients in the placeboedaravone arm than among those in the edaravoneedaravone arm (log-rank test, p<0.001). Conclusions The King's and MiToS staging systems provided utility in assessing clinical progression in Edaravone Study 19. These findings may support the use of staging systems as end points in ALS clinical trials and to understand the timing of benefit as measured by these scales.

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