CA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVECOVER ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


CA Cancer J Clin 2009; 59:111-137
doi: 10.3322/caac.20003
© 2009 American Cancer Society
This Article
Right arrow Full Text Freely available
Right arrow Full Text (PDF) Freely available
Right arrow Freely available CME: Take the course for this article:
Novel Agents on the Horizon for Cancer Therapy
Right arrow An erratum has been published
Right arrow An erratum has been published
Right arrow Submit a letter to the editor
Right arrow View responses
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ma, W. W.
Right arrow Articles by Adjei, A. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ma, W. W.
Right arrow Articles by Adjei, A. A.

Novel Agents on the Horizon for Cancer Therapy

Wen W. Ma, MD1 and Alex A. Adjei, MD, PhD2

1Assistant Professor, Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY
2Senior Vice President, Clinical Research, Chair, Department of Medicine, Katherine Anne Gioia Chair in Cancer Medicine, Roswell Park Cancer Institute, Buffalo, NY

Corresponding author: Alex A. Adjei, MD, PhD, Roswell Park Cancer Institute, Elm & Carlton Streets, Buffalo, NY, 14263; e-mail: Alex.Adjei{at}RoswellPark.org

To earn free CME credit for successfully completing the online quiz based on this article, go to http://CME.AmCancerSoc.org.

DISCLOSURES: Dr. Adjei has received research grants from Eli Lilly and Ardea and honoraria from Array BioPharma. No other conflict of interest relevant to this article was reported.

Although cancer remains a devastating diagnosis, several decades of preclinical progress in cancer biology and biotechnology have recently led to successful development of several biological agents that substantially improve survival and quality of life for some patients. There is now a rich pipeline of novel anticancer agents in early phase clinical trials. The specific tumor and stromal aberrancies targeted can be conceptualized as membrane-bound receptor kinases (HGF/c-Met, human epidermal growth factor receptor and insulin growth factor receptor pathways), intracellular signaling kinases (Src, PI3k/Akt/mTOR, and mitogen-activated protein kinase pathways), epigenetic abnormalities (DNA methyltransferase and histyone deacetylase), protein dynamics (heat shock protein 90, ubiquitin-proteasome system), and tumor vasculature and microenvironment (angiogenesis, HIF, endothelium, integrins). Several technologies are available to target these abnormalities. Of these, monoclonal antibodies and small-molecule inhibitors have been the more successful, and often complementary, approaches so far in clinical settings. The success of this target-based cancer drug development approach is discussed with examples of recently approved agents, such as bevacizumab, erlotinib, trastuzumab, sorafenib, and bortezomib. This review also highlights the pipeline of rationally designed drugs in clinical development that have the potential to impact clinical care in the near future. CA Cancer J Clin 2009;59:111–137. © 2009 American Cancer Society, Inc.




This article has been cited by other articles:


Home page
J Gerontol A Biol Sci Med SciHome page
Z. D. Sharp and R. Strong
The Role of mTOR Signaling in Controlling Mammalian Life Span: What a Fungicide Teaches Us About Longevity
J Gerontol A Biol Sci Med Sci, January 18, 2010; (2010) glp212v1.
[Full Text] [PDF]


Home page
Circ. Res.Home page
H. Cheng and T. Force
Molecular Mechanisms of Cardiovascular Toxicity of Targeted Cancer Therapeutics
Circ. Res., January 8, 2010; 106(1): 21 - 34.
[Abstract] [Full Text] [PDF]


Home page
Am J Health Syst PharmHome page
S. T. Wong
Emerging treatment combinations: Integrating therapy into clinical practice
Am. J. Health Syst. Pharm., December 1, 2009; 66(23_Supplement_6): S9 - S14.
[Abstract] [Full Text] [PDF]


Home page
Ann OncolHome page
S. Park, J. Koo, H. S. Park, J.-H. Kim, S.-Y. Choi, J. H. Lee, B.-W. Park, and K. S. Lee
Expression of androgen receptors in primary breast cancer
Ann. Onc., November 3, 2009; (2009) mdp510v1.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
L. Xu, Y. Ding, W. J. Catalona, X. J. Yang, W. F. Anderson, B. Jovanovic, K. Wellman, J. Killmer, X. Huang, K. A. Scheidt, et al.
MEK4 Function, Genistein Treatment, and Invasion of Human Prostate Cancer Cells
J Natl Cancer Inst, August 19, 2009; 101(16): 1141 - 1155.
[Abstract] [Full Text] [PDF]

eLetters:

Read all eLetters

Novel agents for cancer therapy and cancer multidrug resistance promote an evolutionary arms race
Xiaofang Xu, et al.
CA Online, 27 Jul 2009 [Full text]



HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVECOVER ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by American Cancer Society.