The potential impact of treatment variations on the results of radiotherapy of the internal mammary lymph node chain: A quality-assurance report on the dummy run of EORTC phase III randomized trial 22922/10925 in stage I-III breast cancer

被引:78
作者
Poortmans, PMP
Venselaar, JLM
Struikmans, H
Hurkmans, CW
Davis, JB
Huyskens, D
van Tienhoven, G
Vlaun, V
Lagendijk, JJW
Mijnheer, BJ
De Winter, KA
Van der Hulst, MH
Van den Bogaert, WFC
机构
[1] Dr Bernard Verbeeten Inst, Dept Radiotherapy, NL-5000 LA Tilburg, Netherlands
[2] Univ Utrecht, Med Ctr, Dept Radiotherapy, Utrecht, Netherlands
[3] Antoni Van Leeuwenhoek Huis, Dept Radiotherapy, Amsterdam, Netherlands
[4] Univ Zurich Hosp, Dept Radiotherapy, CH-8091 Zurich, Switzerland
[5] Katholieke Univ Leuven Hosp, Dept Radiotherapy, B-3000 Louvain, Belgium
[6] Univ Amsterdam, Acad Med Ctr, Dept Radiotherapy, NL-1105 AZ Amsterdam, Netherlands
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2001年 / 49卷 / 05期
关键词
quality assurance; breast cancer; radiotherapy; randomized trial; internal mammary node;
D O I
10.1016/S0360-3016(00)01549-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To present the results of the dummy run of the European Organization for Research and Treatment of Cancer (EORTC) trial investigating the role of adjuvant internal mammary and medial supraclavicular (IM-MS) irradiation in Stage I-m breast cancer. Methods and Materials: All participating institutions were asked to produce a treatment plan without (Arm 1) and with (Arm 2) simultaneous IM-MS irradiation of 1 patient after mastectomy and of 1 patient after lumpectomy. Thirty-two dummy runs have been evaluated for compliance to protocol guidelines, with respect to treatment technique and dose prescription. Results: A number of more or less important deviations in treatment setup and prescription have been found. The dose in the IM-MS region deviated significantly from the prescribed dose in 10% of the cases for Arm 1, and in 21% for Arm 2. Assuming a true 5% 10-year survival benefit from optimal IM-MS irradiation, an increase of only 3.8% will be found due to this suboptimal dose distribution. Conclusion: In the dummy run, a number of potential systematic protocol deviations that might lead to false-negative results were detected. By providing recommendations to the participating institutions, we expect to improve the interinstitutional consistency and to promote a high quality irradiation in all institutions participating in the trial. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:1399 / 1408
页数:10
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