Open-Label Placebo for the Treatment of Cancer-Related Fatigue in Patients with Advanced Cancer: A Randomized Controlled Trial

被引:6
|
作者
Yennurajalingam, Sriram [1 ]
Azhar, Ahsan [1 ]
Lu, Zhanni [1 ]
Rodriguez, Ashley J. [1 ]
Arechiga, Adrienne B. [1 ]
Guerra-Sanchez, Maria [1 ]
Stanton, Penny [1 ]
Andersen, Clark R. [2 ]
Urbauer, Diana L. [2 ]
Bruera, Eduardo [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Palliat Care Rehabil Med & Integrat Med, 1515 Holcombe Blvd,Unit 1414, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Biostat, Houston, TX 77030 USA
来源
ONCOLOGIST | 2022年 / 27卷 / 12期
关键词
cancer-related fatigue; treatment; placebo; fatigue cluster; randomized control trial; DOUBLE-BLIND; FUNCTIONAL ASSESSMENT; CLINICAL-TRIALS; VALIDATION; THERAPY; SCALE; METHYLPHENIDATE; DEPRESSION; SYMPTOMS; PAIN;
D O I
10.1093/oncolo/oyac184
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The purpose of this study was to determine the effects of an open-labeled placebo (OLP) compared to a waitlist control (WL) in reducing cancer-related fatigue (CRF) in patients with advanced cancer using Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F). Materials and Methods In this randomized controlled trial, patients with fatigue >= 4/10 on Edmonton Symptom Assessment Scale (ESAS) were randomized to OLP one tablet twice a day or WL for 7 days. On day 8, patients of both arms received a placebo for 3 weeks. Changes in FACIT-F from baseline to day 8 (primary outcome) and at day 29, were assessed. Secondary outcomes included FACT-G, Multidimensional Fatigue Symptom Inventory-SF, Fatigue cluster (defined as a composite of ESAS fatigue, pain, and depression), Center for epidemiologic studies-depression, Godin leisure-time physical activity questionnaire, and global symptom evaluation. Results A total of 84/90 (93%) patients were evaluable. The mean (SD) FACIT-F change at day 8 was 6.6 (7.6) after OLP, vs. 2.1 (9.4) after WL (P = .016). On days 15 and 29, when all patients received OLP, there was a significant improvement in CRF and no difference between arms. There was also a significant improvement in ESAS fatigue, and fatigue cluster score in the OLP arm on day 8 of the study (0.029, and 0.044, respectively). There were no significant differences in other secondary outcomes and adverse events between groups. Conclusions Open-labeled placebo was efficacious in reducing CRF and fatigue clusters in fatigued advanced cancer patients at the end of 1 week. The improvement in fatigue was maintained for 4 weeks. Further studies are needed. This article reports on the effects of an open-labeled placebo compared with wait-list control in reducing cancer-related fatigue in patients with advanced cancer using Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F).
引用
收藏
页码:1081 / 1089
页数:9
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