The past decade has brought an unprecedented focus on the development and clinical utility of targeted therapies in all areas of medicine. This is both a cause and a consequence of realizing the importance of understanding each patient's disease based not only on presenting signs and symptoms, but also, crucially, on fundamental molecular mechanisms. Nowhere has this phenomenon been more prevalent than in oncology. Dysregulation of various membrane receptors, signaling pathways, and other factors occurs frequently in many human malignancies, including breast cancer. Therapeutic approaches targeting these molecules and the selective estrogen receptor modulators and aromatase inhibitors have been demonstrated to have higher efficacy than conventional therapy agents in the treatment of breast cancer. The development of monoclonal antibodies and other inhibitors of specific molecules, fully utilizing the insights learned from molecular techniques such as comparative microarrays and protein expression patterns, has led to the development and FDA approval of several agents for the treatment of breast cancer, such as trastuzamab (Herceptin, targeting HER-2 positive tumors) and lapatinib (Tykerb, targeting tumors with mutated/overexpressed EGFR 1 and 2). Other agents specifically targeting the estrogen receptor, the aromatose pathway and microtubule dynamics, fulvestrant (Faslodex, targeting the ER specifically in breast cancer cells), and letrozole (Femara, targeting the aromatose pathway), raloxifene (Evista, a selective estrogen receptor modulator), ixabepilone (Ixempra, a ?-tubulin inhibitor) have also been approved for various stages and specific settings in breast cancer treatment. The current challenges in the field include further targeting of these agents as part of specific strategies for each patient (biomarker testing, pharmacogenetics, etc.), as well as follow-up and management of adverse events The Oxford American Pocket Notes: Targeted Therapies in Breast Cancer will provide clinicians with the ultra-concise, evidence-based, current information and insight on implementing the latest treatment strategies, including targeted agents, into clinical practice. This portable volume will act as a quick, easily accessible guide for the practicing oncologist, oncology care staff (including nurses and PAs) as well as the primary care practitioner, on the mechanism of action, dosing and administration and adverse effects of the approved targeted agents. The volume features multiple illustrations and tables to highlight key concepts and increase the utility of this resource in clinical practice.

About the Author
Harold J. Burstein, MD, PhD Associate Professor of Medicine Dana Farber Cancer Institute Breast Oncology Center Harvard Medical School Boston, MA

Reviews
'Hal [Harold Burstein] is a friend and I am confident he would do a great job.' -- William J. Gradishar, MD, Professor of Medicine, Northwestern University, Chicago, Illinois; Director, Breast Medical Oncology, Robert H. Lurie Comprehensive Cancer Center, Chicago, Illinois 'Dr. Burstein is certainly a knowledgeable breast cancer expert and is involved in the clinical development of many novel anti cancer drugs, including several molecularly targeted agents. The stated focus of the book appears to b e HER2, EGFR and VEGF, and these targets were selected because each has one or more commercially available 'targeted therapeutic.' -- GN Hortobagyi, MD, FACP, Chairman and Professor in the Department of Breast Medical Oncology, Departments of Breast Medical Oncology and Molecular & Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX



Book Information
ISBN 9780199735679
Author Harold Burstein
Format Paperback
Page Count 64
Imprint Oxford University Press Inc
Publisher Oxford University Press Inc
Weight(grams) 48g
Dimensions(mm) 94mm * 170mm * 8mm