Methylphenidate Versus Placebo for Treating Fatigue in Patients With Advanced Cancer: Randomized, Double-Blind, Multicenter, Placebo-Controlled Trial

被引:4
作者
Stone, Patrick Charles [1 ]
Minton, Ollie [2 ]
Richardson, Alison [3 ,4 ]
Buckle, Peter [1 ]
Enayat, Zinat E. [1 ]
Marston, Louise [5 ]
Freemantle, Nick [6 ]
机构
[1] Univ Coll London UCL, Marie Curie Palliat Care Res Dept, Div Psychiat, London, England
[2] Univ Hosp Sussex NHS Fdn Trust, Worthing Hosp, Lyndhurst Rd, Worthing, England
[3] Univ Southampton, Southampton, England
[4] Univ Hosp Southampton NHS Foundat Trust, Southampton Gen Hosp, Southampton, England
[5] Univ Coll London UCL, Inst Epidemiol & Hlth Care, Fac Populat Hlth Sci, Dept Primary Care & Populat Hlth, London, England
[6] Univ Coll London UCL, Comprehens Clin Trials Unit, London, England
关键词
QUALITY-OF-LIFE; FUNCTIONAL ASSESSMENT; EORTC QLQ-C15-PAL; PALLIATIVE CARE; PHASE-III; DEPRESSION; CHEMOTHERAPY; PREVALENCE; ANEMIA;
D O I
10.1200/JCO.23.02639
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSETo compare effects and side effects of 6 weeks of individually dose-titrated methylphenidate or placebo on fatigue in palliative care patients with advanced cancer. METHODSThis is a randomized, double-blind, placebo-controlled, multicenter trial. Eligible patients had advanced incurable cancer and fatigue >3/10. Principal exclusions were hypertension; psychiatric, cardiovascular, cerebrovascular, renal, liver, or blood disorders; substance dependency; and epilepsy. Patients were randomly assigned 1:1 methylphenidate or placebo starting at 5 mg twice daily. Dose of methylphenidate/placebo was titrated once per week, over 6 weeks, up to a maximum of 20 mg three times daily. Trial ended at 10 weeks. Primary outcome was the difference in Functional Assessment of Chronic Illness Therapy Fatigue (FACIT-F) scores between groups at 6 +/- 2 weeks. Secondary outcomes included adverse effects, quality of life, and mood. RESULTSOne hundred sixty-two patients (73 men; mean, 65.8; standard deviation [SD], 10.3 years) were randomly assigned, and three were excluded from analysis. Seventy-seven were allocated placebo (baseline FACIT-F = 22 [SD, 10]); 82 were allocated methylphenidate (FACIT-F = 20 [SD, 9]). After 6 +/- 2 weeks, FACIT-F scores were 1.97 points (95% CI, -0.95 to 4.90; P = .186) higher (better) on methylphenidate than placebo. Across 10 weeks of the study, FACIT-F was nominally higher in the methylphenidate group versus placebo (Diff, 2.20 [95% CI, 0.39 to 4.01]), but this did not reach the minimally clinically important difference (5-points). At 6 weeks, there were no differences between groups in quality-of-life or symptom domains except for depression scores (nominally reduced in the methylphenidate group: Diff, -1.35 [95% CI, -2.41 to -0.30]). There were no differences in mortality or serious adverse events. CONCLUSIONAfter 6 +/- 2 weeks of treatment, methylphenidate was not superior to placebo for treating fatigue in advanced cancer. Methylphenidate was safe and well-tolerated.
引用
收藏
页码:2382 / 2392
页数:12
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