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

被引:1
|
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
相关论文
共 50 条
  • [31] DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF METHYLPHENIDATE IN OLDER, DEPRESSED, MEDICALLY ILL PATIENTS
    WALLACE, AE
    KOFOED, LL
    WEST, AN
    AMERICAN JOURNAL OF PSYCHIATRY, 1995, 152 (06): : 929 - 931
  • [32] Treating impulsivity with probiotics in adults (PROBIA): study protocol of a multicenter, double-blind, randomized, placebo-controlled trial
    Arteaga-Henriquez, Gara
    Karina Rosales-Ortiz, Silvia
    Arias-Vasquez, Alejandro
    Bitter, Istvan
    Ginsberg, Ylva
    Ibanez-Jimenez, Pol
    Kilencz, Tunde
    Lavebratt, Catharina
    Matura, Silke
    Reif, Andreas
    Rethelyi, Janos
    Richarte, Vanesa
    Rommelse, Nanda
    Siegl, Anne
    Ramos-Quiroga, J. Antoni
    TRIALS, 2020, 21 (01)
  • [33] Treating impulsivity with probiotics in adults (PROBIA): study protocol of a multicenter, double-blind, randomized, placebo-controlled trial
    Gara Arteaga-Henríquez
    Silvia Karina Rosales-Ortiz
    Alejandro Arias-Vásquez
    Istvan Bitter
    Ylva Ginsberg
    Pol Ibañez-Jimenez
    Tünde Kilencz
    Catharina Lavebratt
    Silke Matura
    Andreas Reif
    Janos Rethelyi
    Vanesa Richarte
    Nanda Rommelse
    Anne Siegl
    J. Antoni Ramos-Quiroga
    Trials, 21
  • [34] Efficacy and Safety of Ganduqing Granules in Treating the Common Cold: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial
    Wang, Yilan
    Zhou, Piao
    Wu, Yuxiao
    Cao, Huaqin
    Hao, Wenfeng
    Wang, Fei
    Guo, Jing
    EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2022, 2022
  • [35] Pentoxifylline for the treatment of patients with advanced cirrhosis. A randomized, placebo-controlled, double-blind trial
    Lebrec, Didier
    Thabut, Dominique
    Oberti, Frederic
    Perarnau, Jean-Marc
    Condat, Bertrand
    Barraud, Helene
    Saliba, Faouzi
    Carbonell, Nicolas
    Renard, Philippe
    Ramond, Marie-Jose
    Moreau, Richard
    Poynard, Thierry
    HEPATOLOGY, 2007, 46 (04) : 249A - 250A
  • [36] Treating Alcohol Withdrawal With Oral Baclofen: A Randomized, Double-Blind, Placebo-Controlled Trial
    Lyon, Jeffrey E.
    Khan, Raza A.
    Gessert, Charles E.
    Larson, Pamela M.
    Renier, Colleen M.
    JOURNAL OF HOSPITAL MEDICINE, 2011, 6 (08) : 469 - 474
  • [37] Adalimumab in Severe and Acute Sciatica A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial
    Genevay, Stephane
    Viatte, Sebastien
    Finckh, Axel
    Zufferey, Pascal
    Balague, Federico
    Gabay, Cem
    ARTHRITIS AND RHEUMATISM, 2010, 62 (08): : 2339 - 2346
  • [38] A multicenter, randomized, double-blind, placebo-controlled trial of valproate for agitation associated with dementia
    Tariot, PN
    Thal, L
    Jakimovich, L
    Thomas, R
    Raman, R
    NEUROBIOLOGY OF AGING, 2004, 25 : S189 - S189
  • [39] Effects of Omeprazole on Sleep Disturbance: Randomized Multicenter Double-Blind Placebo-Controlled Trial
    Aimi, Masahito
    Komazawa, Yoshinori
    Hamamoto, Naoharu
    Yamane, Yuko
    Furuta, Koichiro
    Uchida, Yasushi
    Yano, Shozo
    Morita, Miwa
    Oguro, Hiroaki
    Miyake, Tatsuya
    Sugimoto, Toshitsugu
    Nagi, Seiichi
    Naora, Kohji
    Goubaru, Yoshiyuki
    Ishihara, Shunji
    Kinoshita, Yoshikazu
    CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, 2014, 5
  • [40] Sublingual immunotherapy for peanut allergy: A randomized, double-blind, placebo-controlled multicenter trial
    Fleischer, David M.
    Burks, A. Wesley
    Vickery, Brian P.
    Scurlock, Amy M.
    Wood, Robert A.
    Jones, Stacie M.
    Sicherer, Scott H.
    Liu, Andrew H.
    Stablein, Donald
    Henning, Alice K.
    Mayer, Lloyd
    Lindblad, Robert
    Plaut, Marshall
    Sampson, Hugh A.
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 131 (01) : 119 - U184