The impact of concurrent granulocyte macrophage-colony stimulating factor on radiation-induced mucositis in head and neck cancer patients: A double-blind placebo-controlled prospective phase III study by radiation therapy oncology group 9901

被引:45
作者
Ryu, Janice K. [1 ]
Swann, Suzanne
LeVeque, Francis
Scarantino, Charles W.
Johnson, Darlene
Chen, Allan
Fortin, Andre
Pollock, JonDavid
Kim, Harold
Ang, Kian K.
机构
[1] Univ Calif Davis, Med Ctr, Dept Radiat Oncol, Sacramento, CA 95817 USA
[2] Radiat Therapy Oncol Grp, Dept Stat, Philadelphia, PA USA
[3] Wayne State Univ, Harper Hosp, Oral Oncol Dept, Detroit, MI USA
[4] Rex Healthcare Canc Ctr, Raleigh, NC USA
[5] Univ S Florida, H Lee Moffitt Canc Ctr, Div Geriatr Oncol, Tampa, FL 33682 USA
[6] Notre Dame Hosp, Dept Radiat Therapy Oncol, Hotel Dieu, Quebec City, PQ, Canada
[7] Wheeling Hosp, Dept Radiat Oncol, Shiffler Canc Ctr, Wheeling, WV USA
[8] Wayne State Univ, Dept Radiat Oncol, Detroit, MI 48202 USA
[9] Univ Texas, MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX 77030 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 67卷 / 03期
关键词
GM-CSF; radiation mucositis; head-and-neck cancer;
D O I
10.1016/j.ijrobp.2006.09.043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Based on early clinical evidence of potential mucosal protection by granulocyte-macrophage colony stimulating factor (GM-CSF), the Radiation Therapy Oncology Group conducted a double-blind, placebo-controlled, randomized study to test the efficacy and safety of GM-CSF in reducing the severity and duration of mucosal injury and pain (mucositis) associated with curative radiotherapy (RT) in head-and-neck cancer patients. Methods and Materials: Eligible patients included those with head-and-neck cancer with radiation ports encompassing > 50% of oral cavity and/or oropharynx. Standard RT ports were used to cover the primary tumor and regional lymphatics at risk in standard fractionation to 60-70 Gy. Concurrent cisplatin chemotherapy was allowed. Patients were randomized to receive subcutaneous injection of GM-CSF 250 mu g/m(2) or placebo 3 times a week. Mucosal reaction was assessed during the course of RT using the National Cancer Institute Common Toxicity Criteria and the protocol-specific scoring system. Results: Between October 2000 and September 2002, 130 patients from 36 institutions were accrued. Nine patients (7%) were excluded from the analysis, 3 as a result of drug unavailability. More than 80% of the patients participated in the quality-of-life endpoint of this study. The GM-CSF did not cause any increase in toxicity compared with placebo. There was no statistically significant difference in the average mean mucositis score in the GM-CSF and placebo arms by a t test (p = 0.4006). Conclusion: This placebo-controlled, randomized study demonstrated no significant effect of GM-CSF given concurrently compared with placebo in reducing the severity or duration of RT-induced mucositis in patients undergoing definitive RT for head-and-neck cancer. (c) 2007 Elsevier Inc.
引用
收藏
页码:643 / 650
页数:8
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