Lessons learned from radiation oncology clinical trials.

Clin Cancer Res

Authors' Affiliations: Department of Radiation Oncology, Princess Margaret Cancer Center, Toronto, Ontario, Canada; Department of Radiation Oncology, University of Florida Shands Cancer Center, Gainesville, Florida; Radiation Research Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda; Molecular Radiation Therapeutics Branch, Division of Cancer Treatment and Diagnosis, and Clinical Radiation Oncology Branch, National Cancer Institute, Rockville, Maryland; Department of Radiation Oncology, Stanford University, Palo Alto, California; Department of Radiation Oncology, University of Iowa Hospitals and Clinics, Iowa City, Iowa; and Department of Radiation Oncology, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, New York.

Published: November 2013

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965328PMC
http://dx.doi.org/10.1158/1078-0432.CCR-13-1116DOI Listing

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