You are here: Home: Audio Program Guide: BCU 1 | 2006 Audio: BCU 1 | 2006
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Go to interview with Paul Goss, MD, PhD
Go to interview with Charles E Geyer Jr, MD
Go to interview with Peter A Kaufman, MD
Go to interview with Joyce O’Shaughnessy, MD
Go to interview with Aman U Buzdar, MD
Go to interview with Clifford Hudis, MD
Go to interview with Kathy D Miller, MD
Go to interview with Professor John F R Robertson, MB, ChB, BSc, MD |
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To listen to individual tracks now, click the icon. To download tracks to a CD, right-click the icon.
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| Track 1 |
Introduction by Neil Love, MD |
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| Track 2 |
MA17: Extended adjuvant therapy with letrozole
in postmenopausal women |
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| Track 3 |
MA17: Switching to letrozole after placebo |
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| Track 4 |
Use of aromatase inhibitors as initial adjuvant
therapy by clinical investigators |
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| Track 5 |
MA17: Summary of the updated results |
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| Track 6 |
Reduction in the risk of contralateral breast
cancer with aromatase inhibitors |
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| Track 7 |
Risk of recurrence after hormonal therapy |
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| Track 8 |
Evaluating survival in the adjuvant aromatase
inhibitor trials |
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| Track 9 |
Assessing the potential side effects associated
with hormonal therapy |
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| Track 10 |
Impact of aromatase inhibitors on bone
mineral density |
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| Track 11 |
Selection of an aromatase inhibitor as initial
adjuvant therapy |
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| Track 12 |
Optimizing adjuvant hormonal therapy |
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| Track 13 |
Duration of adjuvant therapy with an
aromatase inhibitor |
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| Track 14 |
Delayed adjuvant therapy |
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| Track 15 |
Extended adjuvant letrozole in women with
ER-positive, PR-negative disease |
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| Track 16 |
Optimizing aromatase inhibitors in the treatment
and prevention of breast cancer |
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Charles E Geyer Jr, MD
Director of Medical Affairs
National Surgical Adjuvant Breast
and Bowel Project
Director of Breast Medical Oncology
Allegheny General Hospital
Pittsburgh, Pennsylvania
Click here to download the entire interview |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Cardiac toxicity with adjuvant trastuzumab |
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| Track 3 |
Clinical use of adjuvant trastuzumab based on the
patient’s post-AC left ventricular ejection fraction |
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| Track 4 |
Clinical use of adjuvant trastuzumab in a patient
with low-risk disease |
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| Track 5 |
Impact of adjuvant trastuzumab on distant
recurrence rate |
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| Track 6 |
Future adjuvant trials combining trastuzumab
with lapatinib or bevacizumab |
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| Track 7 |
Clinical use of delayed adjuvant trastuzumab |
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| Track 8 |
Proposed NSABP trial evaluating the
duration of adjuvant therapy with an
aromatase inhibitor |
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| Track 9 |
NSABP-B-40: Neoadjuvant chemotherapy trial |
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| Track 10 |
NSABP-B-41: Phase II randomized trial of
neoadjuvant trastuzumab |
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| Track 11 |
NSABP-B-39: Trial of conventional versus
partial breast irradiation |
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Peter A Kaufman, MD
Associate Professor of Medicine
Section of Hematology/Oncology
Dartmouth-Hitchcock
Medical Center
Comprehensive Breast Care Program
Norris Cotton Cancer Center
Lebanon, New Hampshire
Click here to download the entire interview |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Overview of the adjuvant trastuzumab trials |
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| Track 3 |
NCCTG-N9831: Concurrent versus sequential
adjuvant trastuzumab |
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| Track 4 |
Initiating trastuzumab therapy after discontinuation of an adjuvant anthracycline |
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| Track 5 |
Clinical use of adjuvant trastuzumab in
patients with node-negative disease |
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| Track 6 |
Use of adjuvant trastuzumab in older patients |
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| Track 7 |
Incorporation of adjuvant trastuzumab in a
dose-dense chemotherapy regimen |
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| Track 8 |
Adjuvant trastuzumab monotherapy in
older patients |
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| Track 9 |
Delayed adjuvant trastuzumab |
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| Track 10 |
Controversies in HER2 testing |
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| Track 11 |
Common questions regarding the clinical use
of adjuvant trastuzumab |
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| Track 12 |
Future trials of adjuvant trastuzumab |
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| Track 13 |
Impact of adjuvant trastuzumab data on the
treatment of metastatic disease |
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| Track 14 |
Trastuzumab in combination with liposomal
doxorubicin or capecitabine |
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| Track 15 |
Clinical trials for patients with HER2-negative
disease |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Adjuvant trial comparing docetaxel/
cyclophosphamide versus doxorubicin/
cyclophosphamide |
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| Track 3 |
Adjuvant trial comparing doxorubicin/
cyclophosphamide followed by every three-week paclitaxel versus doxorubicin/paclitaxel
followed by weekly paclitaxel |
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| Track 4 |
Clinical trials combining taxanes and
capecitabine in the adjuvant and
metastatic settings |
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| Track 5 |
Trials of adjuvant dose-dense nanoparticle
albumin-bound (nab) paclitaxel |
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| Track 6 |
Adjuvant chemotherapy for low- and high-risk
patients in the clinical setting |
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| Track 7 |
Dosing and scheduling of capecitabine in the
metastatic setting |
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| Track 8 |
Adjuvant nab paclitaxel in clinical practice |
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Meet The Professors: Aman U Buzdar, MD
Professor of Medicine
Deputy Chairman, Department of
Breast Medical Oncology
The University of Texas MD Anderson
Cancer Center
Houston, Texas
Click here to download the entire interview |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Aromatase inhibitors versus tamoxifen
as initial adjuvant endocrine therapy in postmenopausal
patients |
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| Track 3 |
Safety profiles of the aromatase inhibitors |
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| Track 4 |
Risk of cancer-specific mortality after
recurrence |
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| Track 5 |
Identifying patients who may benefit from
initial adjuvant therapy with tamoxifen |
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| Track 6 |
Tolerability of aromatase inhibitors versus
tamoxifen |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Rationale for dose-dense chemotherapy |
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| Track 3 |
Retrospective analysis of adjuvant chemotherapy
trials CALGB-8541, 9344 and 9741 |
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| Track 4 |
Impact of adjuvant chemotherapy on patients
with ER-positive disease |
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| Track 5 |
Selecting adjuvant chemotherapy based on ER
status and risk of recurrence |
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| Track 6 |
Rationale for increasing the frequency of
dose-dense therapy |
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| Track 7 |
Evaluating dose-dense AC/nab paclitaxel |
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| Track 8 |
Economic impact of newer treatment
alternatives |
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| Track 9 |
Rationale for dose-dense therapy in patients
with ER-positive disease |
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Meet The Professors: Kathy D Miller, MD
Sheila D Ward Scholar of Medicine
Associate Professor of Medicine
Department of Hematology/Oncology
Indiana University
School of Medicine
Indianapolis, Indiana
Click here to download the entire interview |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Rationale and design of the E2100 trial:
Paclitaxel with or without bevacizumab as firstline
treatment for metastatic disease |
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| Track 3 |
Combining bevacizumab with paclitaxel
versus capecitabine |
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| Track 4 |
Identifying patients most likely to benefit from
bevacizumab |
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| Track 5 |
Bevacizumab in the treatment of inflammatory
breast cancer |
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| Track 6 |
Combining capecitabine and bevacizumab in
clinical practice for metastatic disease |
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| Track 7 |
Metronomic chemotherapy plus bevacizumab |
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Meet The Professors: Professor John F R Robertson,
MB,
ChB, BSc, MD
Professor of Surgery
Head of Academic Division
of Breast Surgery
University of Nottingham
City Hospital
Nottingham, United Kingdom
Click here to download the entire interview |
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| Track 1 |
Introduction by Dr Love |
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| Track 2 |
Development of fulvestrant |
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| Track 3 |
Clinical trials of fulvestrant for patients with
disease progression after aromatase inhibitors |
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| Track 4 |
Fulvestrant in treatment of premenopausal
patients with metastatic disease |
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| Track 5 |
Rationale for combining fulvestrant with an
aromatase inhibitor |
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| Track 6 |
Whether to continue an aromatase inhibitor
when adding fulvestrant for disease progression |
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| Track 7 |
LHRH agonist plus endocrine therapy for
premenopausal patients in the adjuvant setting |
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