Lessons Learned from Radiation Oncology Clinical Trials

被引:28
作者
Liu, Fei-Fei [1 ]
Okunieff, Paul [2 ]
Bernhard, Eric J. [3 ]
Stone, Helen B. [3 ]
Yoo, Stephen [4 ]
Coleman, C. Norman [3 ]
Vikram, Bhadrasain [5 ]
Brown, Martin [6 ]
Buatti, John [7 ]
Guha, Chandan [8 ,9 ]
机构
[1] Princess Margaret Canc Ctr, Dept Radiat Oncol, Toronto, ON M5G 2M9, Canada
[2] Univ Florida, Shands Canc Ctr, Dept Radiat Oncol, Gainesville, FL USA
[3] NCI, Radiat Res Program, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
[4] NCI, Mol Radiat Therapeut Branch, Div Canc Treatment & Diag, Rockville, MD 20852 USA
[5] NCI, Clin Radiat Oncol Branch, Rockville, MD 20852 USA
[6] Stanford Univ, Dept Radiat Oncol, Palo Alto, CA 94304 USA
[7] Univ Iowa Hosp & Clin, Dept Radiat Oncol, Iowa City, IA 52242 USA
[8] Albert Einstein Coll Med, Dept Radiat Oncol, Bronx, NY 10467 USA
[9] Montefiore Med Ctr, Bronx, NY 10467 USA
关键词
GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; SQUAMOUS-CELL CARCINOMA; LOCALLY ADVANCED HEAD; LUNG-CANCER; NECK-CANCER; QUALITY-ASSURANCE; ANDROGEN SUPPRESSION; PROSTATE-CANCER; STK33; KINASE;
D O I
10.1158/1078-0432.CCR-13-1116
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A workshop entitled "Lessons Learned from Radiation Oncology Trials" was held on December 7-8, 2011, in Bethesda, MD, to present and discuss some of the recently conducted radiation oncology clinical trials with a focus on those that failed to refute the null hypothesis. The objectives of this workshop were to summarize and examine the questions that these trials provoked, to assess the quality and limitations of the preclinical data that supported the hypotheses underlying these trials, and to consider possible solutions to these challenges for the design of future clinical trials. Several themes emerged from the discussions: (i) opportunities to learn from null-hypothesis trials through tissue and imaging studies; (ii) value of preclinical data supporting the design of combinatorial therapies; (iii) significance of validated biomarkers; (iv) necessity of quality assurance in radiotherapy delivery; (v) conduct of sufficiently powered studies to address the central hypotheses; and (vi) importance of publishing results of the trials regardless of the outcome. The fact that well-designed hypothesis-driven clinical trials produce null or negative results is expected given the limitations of trial design and complexities of cancer biology. It is important to understand the reasons underlying such null results, however, to effectively merge the technologic innovations with the rapidly evolving biology for maximal patient benefit through the design of future clinical trials. (C) 2013 AACR.
引用
收藏
页码:6089 / 6100
页数:12
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