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  Go to interview with Jenny C Chang, MD
Go to interview with I Craig Henderson, MD
Go to interview with Professor Sir Richard Peto

Go to interview with Maura N Dickler, MD
 

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Jenny C Chang, MD
Associate Professor
Breast Center at Baylor College of Medicine
Houston, Texas

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Track 1 Introduction by Neil Love, MD
Track 2 Gene expression profiling to find predictors of response to neoadjuvant docetaxel
Track 3 Differences in predictors of response to docetaxel and AC chemotherapy
Track 4 Developing clinical assays to test for predictors of response to chemotherapeutic agents
Track 5 Induction of apoptosis with neoadjuvant trastuzumab
Track 6 Benefit of testing biologic agents in the neoadjuvant setting


Track 7 Predictors of response to tyrosine kinase inhibitors versus trastuzumab
Track 8 Need for larger trials to confirm MD Anderson neoadjuvant trastuzumab results
Track 9 Biologic rationale for the benefit of pan-HER2 inhibition
Track 10 New clinical research strategies with biologic therapies
Track 11 Cardiac toxicity associated with trastuzumab
Track 12 Nonprotocol use of neoadjuvant and adjuvant trastuzumab
Track 13 Management of HER2-positive metastatic disease
Track 14 Role of fulvestrant in clinical practice
       
I Craig Henderson, MD
Adjunct Professor of Medicine
University of California, San Francisco
San Francisco, California

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Track 1 Introduction by Dr Love
Track 2 Heterogeneity of breast cancer
Track 3 Selection of optimal adjuvant hormonal therapy
Track 4 Difficulty showing survival advantage in adjuvant trials of older patients with low-risk disease
Track 5 Carryover effect with adjuvant hormonal therapy
Track 6 Selection of an aromatase inhibitor versus tamoxifen based on toxicity profiles


Track 7 Time course for switching from tamoxifen to an aromatase inhibitor
Track 8 Limitations of current methods to classify breast cancer
Track 9 Impact of false-negative research findings on drug development
Track 10 New research strategies to identify effective therapies and combinations
Track 11 Ongoing development of novel AKT inhibitor KRX-0401
Track 12 Cancer as a chronic disease
       
Professor Sir Richard Peto
Clinical Trial Service Unit (CTSU)
University of Oxford
Oxford, United Kingdom

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Track 1 Introduction by Dr Love
Track 2 Impact of all-cause mortality on clinical trial results
Track 3 Carryover effect of therapies for the treatment of breast cancer
Track 4 Rationale for reductions in breast cancer mortality over the past 10 years
Track 5 Impact of screening mammography on decreases in breast cancer mortality
Track 6 Extended adjuvant tamoxifen: ATLAS and aTTom trials
Track 7 Impact of CAN-NCIC-MA17 results on the ongoing ATLAS trial
Track 8 False-negative ER assays
Track 9 Relationship between ER status of primary and contralateral breast cancers
Track 10 Role of ovarian ablation in combination with other effective therapies
Track 11 Need for clinical trials of adjuvant chemotherapy in elderly women
Track 12 Impact of local tumor control on breast cancer mortality
Track 13 Cardiac effects of postmastectomy radiotherapy
       
Maura N Dickler, MD
Assistant Attending Physician
Breast Cancer Medicine Service
Memorial Sloan-Kettering Cancer Center
New York, New York

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Track 1 Introduction by Dr Love
Track 2 Phase II trial of bevacizumab and erlotinib for patients with metastatic disease
Track 3 Potential value of measuring circulating tumor cells
Track 4 Response rates of single-agent bevacizumab and tyrosine kinase inhibitors in breast cancer


Track 5 Management of patients with HER2-positive metastatic disease
Track 6 Benefit of avoiding premedication with nanoparticle paclitaxel
Track 7 Potential role of nanoparticle paclitaxel in clinical practice
Track 8 Selection of combination chemotherapy in the metastatic setting
Track 9 Benefits of treating patients with capecitabine
Track 10 Rationale for up-front use of adjuvant anastrozole
Track 11 Time course for initiating an aromatase inhibitor after five years of tamoxifen
Track 12 Nonprotocol use of neoadjuvant and adjuvant trastuzumab
Track 13 Patient preferences for oral versus parenteral endocrine therapy