Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/71930
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Tumor control versus adverse events with targeted anticancer therapies
Author: Keefe, D.
Bateman, E.
Citation: Nature Reviews Clinical Oncology, 2012; 9(2):98-109
Publisher: Nature Publishing Group
Issue Date: 2012
ISSN: 1759-4774
1759-4782
Statement of
Responsibility: 
Dorothy M.K. Keefe and Emma H. Bateman
Abstract: The advent of targeted anticancer therapies over the past few decades has reinvigorated the field of cancer therapeutics, with the promise of increased cancer cure rates accompanied by decreased toxicity. But, has that promise been fulfilled? The short answer is definitely ‘no’, both because of disappointing tumor responses and unexpectedly high toxicity, as well as the extremely high financial cost of these agents. However, failing to completely fulfill initial promise does not mean that targeted therapies should be abandoned. Increased progression-free survival might ultimately lead to increased overall survival, and targeted therapies have changed the course of cancers such as breast, lung and renal. Therefore, we would argue that despite some disappointments, targeted therapies have a vital role in future cancer treatment. This Review will discuss the positives and negatives of targeted agents, and propose a way to optimize their use and development to ensure proper personalized cancer medicine that tailors not only the anticancer treatment, but also the antitoxicity strategies, to achieve the best outcome for the patient in terms of both quality and quantity of life.
Keywords: Humans; Neoplasms; Clinical Trials as Topic; Molecular Targeted Therapy; Precision Medicine
Rights: © 2012 Macmillan Publishers Limited. All rights reserved
RMID: 0020116570
DOI: 10.1038/nrclinonc.2011.192
Appears in Collections:Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.