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I-SPY 2: An Adaptive Breast Cancer Trial Design in the Setting of Neoadjuvant Chemotherapy
Clinical Pharmacology & Therapeutics · 2009 · Vol. 86(1) · pp. 97–100
AD Barker✉(National Cancer Institute)C C Sigman✉(CCS Associates (United States))Kelloff Gj(National Cancer Institute)NM Hylton(University of California, San Francisco)DA Berry(The University of Texas MD Anderson Cancer Center)L. Esserman(University of California, San Francisco)
Abstract
I-SPY 2 (investigation of serial studies to predict your therapeutic response with imaging and molecular analysis 2) is a process targeting the rapid, focused clinical development of paired oncologic therapies and biomarkers. The framework is an adaptive phase II clinical trial design in the neoadjuvant setting for women with locally advanced breast cancer. I-SPY 2 is a collaborative effort among academic investigators, the National Cancer Institute, the US Food and Drug Administration, and the pharmaceutical and biotechnology industries under the auspices of the Foundation for the National Institutes of Health Biomarkers Consortium.
Biosimilars and Bioanalytical MethodsStatistical Methods in Clinical TrialsHealth Systems, Economic Evaluations, Quality of LifeBreast cancerMedicineClinical trialFood and drug administrationOncologyDrug developmentClinical OncologyInternal medicineNeoadjuvant therapyChemotherapy
MeSH terms
Breast NeoplasmsClinical Trials as TopicFemaleHumansBiomarkersDrugs, InvestigationalClinical Trials, Phase I as TopicNeoadjuvant Therapy
Citations
756
FWCI
13.86
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References
11
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99%
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