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Track 1 |
Introduction by Neil Love, MD |
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Track 2 |
Gene expression profiling to find predictors of response to neoadjuvant docetaxel |
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Track 3 |
Differences in predictors of response to docetaxel and AC chemotherapy |
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Track 4 |
Developing clinical assays to test for predictors of response to chemotherapeutic agents |
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Track 5 |
Induction of apoptosis with neoadjuvant trastuzumab |
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Track 6 |
Benefit of testing biologic agents in the neoadjuvant setting |
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Track 7 |
Predictors of response to tyrosine kinase inhibitors versus trastuzumab |
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Track 8 |
Need for larger trials to confirm MD Anderson neoadjuvant trastuzumab results |
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Track 9 |
Biologic rationale for the benefit of pan-HER2 inhibition |
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Track 10 |
New clinical research strategies with biologic therapies |
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Track 11 |
Cardiac toxicity associated with trastuzumab |
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Track 12 |
Nonprotocol use of neoadjuvant and adjuvant trastuzumab |
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Track 13 |
Management of HER2-positive metastatic disease |
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Track 14 |
Role of fulvestrant in clinical practice |
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Track 1 |
Introduction by Dr Love |
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Track 2 |
Heterogeneity of breast cancer |
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Track 3 |
Selection of optimal adjuvant hormonal therapy |
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Track 4 |
Difficulty showing survival advantage in adjuvant trials of older patients with low-risk disease |
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Track 5 |
Carryover effect with adjuvant hormonal therapy |
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Track 6 |
Selection of an aromatase inhibitor versus tamoxifen based on toxicity profiles |
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Track 7 |
Time course for switching from tamoxifen to an aromatase inhibitor |
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Track 8 |
Limitations of current methods to classify breast cancer |
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Track 9 |
Impact of false-negative research findings on drug development |
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Track 10 |
New research strategies to identify effective therapies and combinations |
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Track 11 |
Ongoing development of novel AKT inhibitor KRX-0401 |
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Track 12 |
Cancer as a chronic disease |
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Track 1 |
Introduction by Dr Love |
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Track 2 |
Impact of all-cause mortality on clinical trial results |
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Track 3 |
Carryover effect of therapies for the treatment of breast cancer |
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Track 4 |
Rationale for reductions in breast cancer mortality over the past 10 years |
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Track 5 |
Impact of screening mammography on decreases in breast cancer mortality |
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Track 6 |
Extended adjuvant tamoxifen: ATLAS and aTTom trials |
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Track 7 |
Impact of CAN-NCIC-MA17 results on the ongoing ATLAS trial |
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Track 8 |
False-negative ER assays |
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Track 9 |
Relationship between ER status of primary and contralateral breast cancers |
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Track 10 |
Role of ovarian ablation in combination with other effective therapies |
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Track 11 |
Need for clinical trials of adjuvant chemotherapy in elderly women |
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Track 12 |
Impact of local tumor control on breast cancer mortality |
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Track 13 |
Cardiac effects of postmastectomy radiotherapy |
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Track 1 |
Introduction by Dr Love |
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Track 2 |
Phase II trial of bevacizumab and erlotinib for patients with metastatic disease |
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Track 3 |
Potential value of measuring circulating tumor cells |
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Track 4 |
Response rates of single-agent bevacizumab and tyrosine kinase inhibitors in breast cancer |
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Track 5 |
Management of patients with HER2-positive metastatic disease |
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Track 6 |
Benefit of avoiding premedication with nanoparticle paclitaxel |
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Track 7 |
Potential role of nanoparticle paclitaxel in clinical practice |
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Track 8 |
Selection of combination chemotherapy in the metastatic setting |
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Track 9 |
Benefits of treating patients with capecitabine |
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Track 10 |
Rationale for up-front use of adjuvant anastrozole |
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Track 11 |
Time course for initiating an aromatase inhibitor after five years of tamoxifen |
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Track 12 |
Nonprotocol use of neoadjuvant and adjuvant trastuzumab |
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Track 13 |
Patient preferences for oral versus parenteral endocrine therapy |
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