The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: longitudinal natural history observations over 48 weeks from a multicenter study

Craig M McDonald, Erik K Henricson, R Ted Abresch, Julaine M Florence, Michelle Eagle, Eduard Gappmaier, Allan M Glanzman, PTC124-GD-007-DMD Study Group, Robert Spiegel, Jay Barth, Gary Elfring, Allen Reha, Stuart Peltz, Monique Ryan, Kristi Jones, Nathalie Goemans, Craig Campbell, Jean Mah, Kathryn Selby, Thomas Voit, Brigitte Chabrol, Yann Pereon, Ulrike Schara, Janberndt Kirschner, Enrico Bertini, Eugenio Mercuri, Giacomo Comi, Yoram Nevo, Juan Vilchez, Jaume Colomer, Sylvia Children, Mar Tulinius, Thomas Sejersen, Katherine Bushby, Francesco Muntoni, Rosaline Christina Mary Quinlivan, Brenda Wong, Richard S Finkel, Jacinda B Sampson, Kevin M Flanigan, Russell Butterfield, John W Day, Katherine Mathews, Basil T Darras, Susan D Apkon, Julie Parsons, Richard Barohn, Anne Connolly, Susan Iannaccone, Douglas M Sproule, Petra Kaufman, Jay J Han, Nanette C Joyce, J Ben Renfroe, Barry S Russman, Stephanie Burns-Wechsler, Steven A Moore, H Lee Sweeney, Kim Coleman, Craig M McDonald, Erik K Henricson, R Ted Abresch, Julaine M Florence, Michelle Eagle, Eduard Gappmaier, Allan M Glanzman, PTC124-GD-007-DMD Study Group, Robert Spiegel, Jay Barth, Gary Elfring, Allen Reha, Stuart Peltz, Monique Ryan, Kristi Jones, Nathalie Goemans, Craig Campbell, Jean Mah, Kathryn Selby, Thomas Voit, Brigitte Chabrol, Yann Pereon, Ulrike Schara, Janberndt Kirschner, Enrico Bertini, Eugenio Mercuri, Giacomo Comi, Yoram Nevo, Juan Vilchez, Jaume Colomer, Sylvia Children, Mar Tulinius, Thomas Sejersen, Katherine Bushby, Francesco Muntoni, Rosaline Christina Mary Quinlivan, Brenda Wong, Richard S Finkel, Jacinda B Sampson, Kevin M Flanigan, Russell Butterfield, John W Day, Katherine Mathews, Basil T Darras, Susan D Apkon, Julie Parsons, Richard Barohn, Anne Connolly, Susan Iannaccone, Douglas M Sproule, Petra Kaufman, Jay J Han, Nanette C Joyce, J Ben Renfroe, Barry S Russman, Stephanie Burns-Wechsler, Steven A Moore, H Lee Sweeney, Kim Coleman

Abstract

Introduction: Duchenne muscular dystrophy (DMD) subjects ≥5 years with nonsense mutations were followed for 48 weeks in a multicenter, randomized, double-blind, placebo-controlled trial of ataluren. Placebo arm data (N = 57) provided insight into the natural history of the 6-minute walk test (6MWT) and other endpoints.

Methods: Evaluations performed every 6 weeks included the 6-minute walk distance (6MWD), timed function tests (TFTs), and quantitative strength using hand-held myometry.

Results: Baseline age (≥7 years), 6MWD, and selected TFT performance are strong predictors of decline in ambulation (Δ6MWD) and time to 10% worsening in 6MWD. A baseline 6MWD of <350 meters was associated with greater functional decline, and loss of ambulation was only seen in those with baseline 6MWD <325 meters. Only 1 of 42 (2.3%) subjects able to stand from supine lost ambulation.

Conclusion: Findings confirm the clinical meaningfulness of the 6MWD as the most accepted primary clinical endpoint in ambulatory DMD trials.

Keywords: 6-minute walk test; Duchenne muscular dystrophy; ambulation; dystrophinopathy; myometry; natural history; prediction of loss of function; timed function tests.

Copyright © 2013 Wiley Periodicals, Inc.

Figures

FIGURE 1
FIGURE 1
Change in strength for 5 strength measures by myometry obtained every 6 weeks for 48 weeks (mean ± SEM) in DMD patients (n = 57).
FIGURE 2
FIGURE 2
(a) Change in baseline time to stand from supine in seconds (mean ± SEM) for steroid-treated patients ≥7 years old (n = 32) and <7 years old (n = 6) with DMD over 48 weeks of evaluation. (b) Change in time to climb 4 stairs in seconds (mean ± SEM) for steroid-treated patients ≥7 years old (n = 34) and <7 years old (n = 6) with DMD over 48 weeks of evaluation. (c) Change in baseline time to run/walk 10 m in seconds (mean ± SEM) for steroid-treated patients ≥7 years old (n = 34) and <7 years old (n = 6) with DMD over 48 weeks of evaluation.
FIGURE 3
FIGURE 3
Relationship between percent change in 6MWD and percent change in 10-m run/walk test.
FIGURE 4
FIGURE 4
(a) Change in 6MWD over 48 weeks in 57 placebo-treated DMD patients. (b) Change in percent predicted 6MWD using age and height − calculated value over 48 weeks in 57 placebo-treated patients.
FIGURE 5
FIGURE 5
Change from baseline 6MWD in meters (mean ± SEM) over 48 weeks by baseline 6MWD level (

FIGURE 6

(a) 6MWD in meters (mean…

FIGURE 6

(a) 6MWD in meters (mean ± SEM) for all placebo-treated patients. (b) Percent…
FIGURE 6
(a) 6MWD in meters (mean ± SEM) for all placebo-treated patients. (b) Percent predicted 6MWD (mean ± SEM) using age and height − calculated value for all placebo-treated patients. (c) Change in 6MWD in meters (mean ± SEM) for steroid-treated DMD patients <7 years old (n = 6) and ≥7 years old (N = 34). (d) Change in percent predicted 6MWD (mean + SEM) using age and height − calculated value for steroid-treated DMD patients <7 years old (n = 6) and ≥7 years old (N = 34).

FIGURE 7

(a) 6MWD in meters (mean…

FIGURE 7

(a) 6MWD in meters (mean ± SEM) for DMD patients <7 years old…
FIGURE 7
(a) 6MWD in meters (mean ± SEM) for DMD patients <7 years old treated with steroids (n = 6) and steroid-naive patients (N = 8). (b) 6MWD in meters (mean ± SEM) for DMD patients ≥7 years old treated with steroids (N = 34) and steroid-naive subjects (N = 9).

FIGURE 8

Time to persistent 10% 6MWD…

FIGURE 8

Time to persistent 10% 6MWD worsening in 57 DMD patients. Note that the…

FIGURE 8
Time to persistent 10% 6MWD worsening in 57 DMD patients. Note that the relative proportion of patients who reached the 10% progression milestone was constant over 48 weeks (26.3% patients declined 10% or more during the first 24 weeks; 23.8% of the remaining patients declined 10% or more from weeks 24–48).

FIGURE 9

(a) Kaplan–Meier analysis of time…

FIGURE 9

(a) Kaplan–Meier analysis of time to 10% progression in 6MWD by time to…
FIGURE 9
(a) Kaplan–Meier analysis of time to 10% progression in 6MWD by time to stand for 3 groups (time to stand <4 s, 4 to < 8 s, and ≥8 s/cannot stand). (b) Kaplan–Meier analysis of time to 10% worsening in 6MWD by time to climb 4 stairs for 3 groups (time to climb 4 stairs <3 s, 3 to <6 s, and ≥6 s/cannot climb). (c) Kaplan–Meier analysis of time to 10% worsening in 6MWD by time to run/walk 10 m for 3 groups (10-m run/walk <5 s, 5 to <10 s, and ≥10 seconds).

FIGURE 10

(a) Kaplan–Maier survival for time…

FIGURE 10

(a) Kaplan–Maier survival for time to 10% progression on 6MWD for 3 groups,…
FIGURE 10
(a) Kaplan–Maier survival for time to 10% progression on 6MWD for 3 groups, based on initial 6MWD (<325 m, 325 to <410 m, and ≥410 m). (b) Kaplan–Meier analysis of time to 10% worsening in 6MWD based on initial percent predicted 6MWD at baseline for 3 groups (percent predicted 6MWD <55%, percent predicted 6MWD 55% to <80%, and percent predicted 6MWD ≥80%).
All figures (10)
FIGURE 6
FIGURE 6
(a) 6MWD in meters (mean ± SEM) for all placebo-treated patients. (b) Percent predicted 6MWD (mean ± SEM) using age and height − calculated value for all placebo-treated patients. (c) Change in 6MWD in meters (mean ± SEM) for steroid-treated DMD patients <7 years old (n = 6) and ≥7 years old (N = 34). (d) Change in percent predicted 6MWD (mean + SEM) using age and height − calculated value for steroid-treated DMD patients <7 years old (n = 6) and ≥7 years old (N = 34).
FIGURE 7
FIGURE 7
(a) 6MWD in meters (mean ± SEM) for DMD patients <7 years old treated with steroids (n = 6) and steroid-naive patients (N = 8). (b) 6MWD in meters (mean ± SEM) for DMD patients ≥7 years old treated with steroids (N = 34) and steroid-naive subjects (N = 9).
FIGURE 8
FIGURE 8
Time to persistent 10% 6MWD worsening in 57 DMD patients. Note that the relative proportion of patients who reached the 10% progression milestone was constant over 48 weeks (26.3% patients declined 10% or more during the first 24 weeks; 23.8% of the remaining patients declined 10% or more from weeks 24–48).
FIGURE 9
FIGURE 9
(a) Kaplan–Meier analysis of time to 10% progression in 6MWD by time to stand for 3 groups (time to stand <4 s, 4 to < 8 s, and ≥8 s/cannot stand). (b) Kaplan–Meier analysis of time to 10% worsening in 6MWD by time to climb 4 stairs for 3 groups (time to climb 4 stairs <3 s, 3 to <6 s, and ≥6 s/cannot climb). (c) Kaplan–Meier analysis of time to 10% worsening in 6MWD by time to run/walk 10 m for 3 groups (10-m run/walk <5 s, 5 to <10 s, and ≥10 seconds).
FIGURE 10
FIGURE 10
(a) Kaplan–Maier survival for time to 10% progression on 6MWD for 3 groups, based on initial 6MWD (<325 m, 325 to <410 m, and ≥410 m). (b) Kaplan–Meier analysis of time to 10% worsening in 6MWD based on initial percent predicted 6MWD at baseline for 3 groups (percent predicted 6MWD <55%, percent predicted 6MWD 55% to <80%, and percent predicted 6MWD ≥80%).

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