Acupuncture for dysphagia after chemoradiation in head and neck cancer: Rationale and design of a randomized, sham-controlled trial

被引:17
|
作者
Lu, Weidong [1 ]
Wayne, Peter M. [2 ,3 ]
Davis, Roger B. [4 ]
Buring, Julie E. [2 ,3 ]
Li, Hailun [5 ]
Goguen, Laura A. [6 ]
Rosenthal, David S. [1 ]
Tishler, Roy B. [7 ]
Posner, Marshall R. [7 ]
Haddad, Robert I. [7 ]
机构
[1] Dana Farber Canc Inst, Leonard P Zakim Ctr Integrat Therapies, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Osher Ctr Integrat Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[5] Dana Farber Harvard Canc Ctr, Boston, MA USA
[6] Brigham & Womens Hosp, Dept Surg, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Head & Neck Oncol Program, Boston, MA 02215 USA
关键词
Acupuncture; Chemoradiation therapy; Head and neck cancer; Dysphagia; MDADI; Randomized sham-controlled trial; QUALITY-OF-LIFE; SALIVARY FLOW-RATES; INTENSITY-MODULATED RADIOTHERAPY; PERFORMANCE STATUS SCALE; LOCALLY ADVANCED HEAD; RADIATION-THERAPY; CHEMOTHERAPY; XEROSTOMIA; INTERVENTIONS; QUESTIONNAIRE;
D O I
10.1016/j.cct.2012.02.017
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Dysphagia is a common side effect following chemoradiation therapy (CRT) in head and neck cancer (HNC) patients. Current dysphagia management includes swallowing therapy and dilation procedures, but these treatments have limitations. While acupuncture has been reported to positively impact swallowing function and quality of life (QOL) in patients with dysphagia, current evidence is inconclusive. Material and methods: In an ongoing trial, 42 squamous cell carcinoma HNC patients, who are receiving platinum-based CRT with curative intent, are being recruited from a comprehensive cancer center. They are randomized to 12 sessions of either active acupuncture or to sham acupuncture during and following CRT over a 24-week period. Blinded research staff assesses outcomes at baseline, 20 weeks post-CRT (end of acupuncture), and 12 months after baseline (6-month follow-up). The primary outcome is change in M.D. Anderson Dysphagia Inventory score from baseline to 12 months. Secondary outcomes include QOL measures pertaining to HNC patients. In addition, a subset of study patients are tested for salivary flow rates and cytokines, including plasma transforming growth factor-beta 1 and interleukin 6 (n = 10 per arm), to preliminarily explore the biological mechanisms of acupuncture for dysphagia. Discussion: This paper addresses unique challenges related to study design in nonpharmacological, sham-controlled acupuncture trials including development of evidence-based credible verum and sham treatment protocols, blinding, and assuring fidelity of treatment. Results of this study will inform the feasibility of conducting a large scale trial and will provide preliminary evidence regarding the value of acupuncture for dysphagia in HNC patients. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:700 / 711
页数:12
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