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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 BarkerC C SigmanKelloff GjNM HyltonDA BerryL. Esserman

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
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