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Influence of Unrecognized
Molecular Heterogeneity
on Randomized Clinical
Trials
By Rebecca A. Betensky, David N. Louis, J. Gregory Cairncross
From the Department of Biostatistics, Harvard School of Public Health and Department of Pathology
and Neurosurgical Service, Massachusetts General Hospital and Harvard Medical School, Boston, MA,
and the Department of Oncology, University of Western Ontario and the London Regional Cancer
Centre, London, Ontario, Canada.
Address reprint requests to Rebecca A. Betensky, PhD, Harvard School of Public Health, 655 Huntington
Ave, Boston, MA 02115; email: betensky@hsph.harvard.edu.
PURPOSE: In solid tumor oncology, decisions regarding treatment and eligibility for
trials are governed by histologic diagnosis.
Despite this reliance on histology and the
assumption that histology defines the disease, underlying molecular heterogeneity likely
differentiates among patients’ outcomes.
PATIENTS AND METHODS: To illustrate how unrecognized molecular heterogeneity
might obscure a truly effective new therapy for cancer, we analyzed the planning
assumptions and results of a hypothetical randomized controlled trial of
chemoradiotherapy for a cancer found to be drug sensitive in preliminary phase II
studies.
RESULTS: Randomized controlled trials of effective cancer therapies can be falsely
negative if therapeutic benefit is overestimated during study design because of
enrichment of phase II trials for treatment-sensitive subtypes, a beneficial effect in
responding patients is diluted by large numbers of nonresponding patients, or a
beneficial effect in responders is reversed by a negative effect in nonresponders.
CONCLUSION: Molecular heterogeneity, if it confers different risks to patients and is
unaccounted for in the design of a randomized study, can result in a clinical trial that is
underpowered and fails to detect a truly effective new therapy for cancer.
Journal of Clinical Oncology, Vol 20, Issue 10 (May),
2002: 2495-2499
© 2002 American Society for Clinical Oncology
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