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Randomized Controlled Trial
. 2017 Dec 5;318(21):2089-2098.
doi: 10.1001/jama.2017.17437.

Effect of Granulocyte-Macrophage Colony-Stimulating Factor With or Without Supervised Exercise on Walking Performance in Patients With Peripheral Artery Disease: The PROPEL Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Effect of Granulocyte-Macrophage Colony-Stimulating Factor With or Without Supervised Exercise on Walking Performance in Patients With Peripheral Artery Disease: The PROPEL Randomized Clinical Trial

Mary M McDermott et al. JAMA. .

Abstract

Importance: Benefits of granulocyte-macrophage colony-stimulating factor (GM-CSF) for improving walking ability in people with lower extremity peripheral artery disease (PAD) are unclear. Walking exercise may augment the effects of GM-CSF in PAD, since exercise-induced ischemia enhances progenitor cell release and may promote progenitor cell homing to ischemic calf muscle.

Objectives: To determine whether GM-CSF combined with supervised treadmill exercise improves 6-minute walk distance, compared with exercise alone and compared with GM-CSF alone; to determine whether GM-CSF alone improves 6-minute walk more than placebo and whether exercise improves 6-minute walk more than an attention control intervention.

Design, setting, and participants: Randomized clinical trial with 2 × 2 factorial design. Participants were identified from the Chicago metropolitan area and randomized between January 6, 2012, and December 22, 2016, to 1 of 4 groups: supervised exercise + GM-CSF (exercise + GM-CSF) (n = 53), supervised exercise + placebo (exercise alone) (n = 53), attention control + GM-CSF (GM-CSF alone) (n = 53), attention control + placebo (n = 51). The final follow-up visit was on August 15, 2017.

Interventions: Supervised exercise consisted of treadmill exercise 3 times weekly for 6 months. The attention control consisted of weekly educational lectures by clinicians for 6 months. GM-CSF (250 μg/m2/d) or placebo were administered subcutaneously (double-blinded) 3 times/wk for the first 2 weeks of the intervention.

Main outcomes and measures: The primary outcome was change in 6-minute walk distance at 12-week follow-up (minimum clinically important difference, 20 m). P values were adjusted based on the Hochberg step-up method.

Results: Of 827 persons evaluated, 210 participants with PAD were randomized (mean age, 67.0 [SD, 8.6] years; 141 [67%] black, 82 [39%] women). One hundred ninety-five (93%) completed 12-week follow-up. At 12-week follow-up, exercise + GM-CSF did not significantly improve 6-minute walk distance more than exercise alone (mean difference, -6.3 m [95% CI, -30.2 to +17.6]; P = .61) or more than GM-CSF alone (mean difference, +28.7 m [95% CI, +5.1 to +52.3]; Hochberg-adjusted P = .052). GM-CSF alone did not improve 6-minute walk more than attention control + placebo (mean difference, -1.4 m [95% CI, -25.2 to +22.4]; P = .91). Exercise alone improved 6-minute walk compared with attention control + placebo (mean difference, +33.6 m [95% CI, +9.4 to +57.7]; Hochberg-adjusted P = .02).

Conclusions and relevance: Among patients with PAD, supervised treadmill exercise significantly improved 6-minute walk distance compared with attention control + placebo, whereas GM-CSF did not significantly improve walking performance, either when used alone or when combined with supervised treadmill exercise. These results confirm the benefits of exercise but do not support using GM-CSF to treat walking impairment in patients with PAD.

Trial registration: clinicaltrials.gov Identifier: NCT01408901.

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Conflict of interest statement

Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr McDermott reported receiving research funding from Novartis and receipt of study drug for another peripheral artery disease study from ReserveAge. Dr Stein reported receiving royalties from the Wisconsin Alumni Research Foundation for intellectual property related to carotid ultrasound and arterial age and serving on a data and safety monitoring board for Lily. Dr Taylor reported that she is cofounder of, but receives no compensation from, Stem Cell Security. Dr Skelly reported having editor royalty agreements with Springer and Inside Ultrasound and that he is cofounder of Maji Therapeutics. No other authors reported disclosures.

Figures

Figure 1.
Figure 1.. Eligible Participants and Follow-up Among People Evaluated for the PROPEL Trial
GM-CSF indicates granulocyte-macrophage colony-stimulating factor; MMSE, Mini–Mental State Examination; PAD, peripheral artery disease; PROPEL, Progenitor Cell Release Plus Exercise to Improve Functional Performance in PAD. aData were imputed for participants who were lost to follow-up or who canceled the visit.
Figure 2.
Figure 2.. Changes in 6-Minute Walk Distance by Study Intervention (N = 208)
Results are based on multiple imputation and exclude 2 participants who died before 12-week follow-up testing and 1 participant who died before 24-week follow-up. Data markers indicate means; error bars, 95% confidence intervals.

References

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