QUANTITATIVE ANALYSES OF NORMAL TISSUE EFFECTS IN THE CLINIC (QUANTEC): AN INTRODUCTION TO THE SCIENTIFIC ISSUES

被引:802
作者
Bentzen, Soren M. [1 ,2 ,3 ]
Constine, Louis S. [4 ]
Deasy, Joseph O. [5 ]
Eisbruch, Avi [6 ]
Jackson, Andrew [7 ]
Marks, Lawrence B. [8 ]
Ten Haken, Randall K. [6 ]
Yorke, Ellen D. [7 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Human Oncol, Madison, WI 53792 USA
[2] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med Phys, Madison, WI 53792 USA
[3] Univ Wisconsin, Sch Med & Publ Hlth, Dept Biostat & Med Informat, Madison, WI 53792 USA
[4] Univ Rochester, Med Ctr, Dept Radiat Oncol, Rochester, NY 14642 USA
[5] Washington Univ, Dept Radiat Oncol, St Louis, MO USA
[6] Univ Michigan, Dept Radiat Oncol, Ann Arbor, MI 48109 USA
[7] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY 10021 USA
[8] Univ N Carolina, Dept Radiat Oncol, Chapel Hill, NC USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2010年 / 76卷 / 03期
关键词
QUANTEC; Normal tissue complications; Overview; Modeling; RADIATION-INDUCED PNEUMONITIS; DOSE-VOLUME; PROSTATE-CANCER; RADICAL RADIOTHERAPY; NECK-CANCER; SPINAL-CORD; MOUSE LUNG; IRRADIATION; TOLERANCE; TOXICITY;
D O I
10.1016/j.ijrobp.2009.09.040
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advances in dose-volume/outcome (or normal tissue complication probability, NTCP) modeling since the seminal Emami paper from 1991 are reviewed. There has been some progress with an increasing number of studies on large patient samples with three-dimensional dosimetry. Nevertheless, NTCP models are not ideal. Issues related to the grading of side effects, selection of appropriate statistical methods, testing of internal and external model validity, and quantification of predictive power and statistical uncertainty, all limit the usefulness of much of the published literature. Synthesis (meta-analysis) of data from multiple studies is often impossible because of suboptimal primary analysis, insufficient reporting and variations in the models and predictors analyzed. Clinical limitations to the current knowledge base include the need for more data on the effect of patient-related cofactors, interactions between dose distribution and cytotoxic or molecular targeted agents, and the effect of dose fractions and overall treatment time in relation to nonuniform dose distributions. Research priorities for the next 5-10 years are proposed. (C) 2010 Elsevier Inc.
引用
收藏
页码:S3 / S9
页数:7
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