New Class of Drugs Brings Hope to Cancer Patients
by: ARA Content
This is an exciting time in cancer research.
Recent information on angiogenesis -- the growth of new blood
vessels -- is providing researchers opportunities to find new
ways to slow or stop a tumor's growth by cutting off the blood
supply it needs.
Angiogenesis performs a critical role in the
development of cancer. To grow, solid tumors need oxygen and nutrients
provided by new blood vessels. Once a vascular network has been
generated, cancer cells can also invade the rest of the body,
a process called metastasis. Currently, researchers believe that
more than 90 percent of all cancer cases are angiogenesis-dependent.
The good news is that a novel class of drugs, which acts as angiogenesis
inhibitors, shows great potential in fighting more than 20 different
diseases, including many types of cancer.
These "anti-angiogenesis" drugs being developed
and tested block the formation of new blood vessels, starving
cancerous cells and stopping tumor growth. One drug being tested,
Neovastat, was discovered in 1994 and is derived from cartilage
tissue. Neovastat is the only angiogenesis inhibitor being developed
in the biotechnology and pharmaceutical universe that has four
mechanisms of action to combat blood vessel growth. Furthermore,
Neovastat is taken orally, making it convenient for patients who
need long-term treatment, and it has shown minimal side effects
in clinical trials. This means that unlike standard chemotherapy,
Neovastat is not likely to interfere with a patient's immune system,
or cause adverse gastrointestinal symptoms or hair loss.
In addition, because most cancer cells are genetically unstable
and more prone to mutations, resistance is a major problem with
many chemotherapy agents. But since anti-angiogenesis drugs target
normal endothelial cells that are not genetically unstable, drug
resistance is less likely to develop and has not been a problem
so far in clinical trials.
Another hope is that angiogenesis inhibitors can be used in combination
with therapies that directly target tumor cells. Because anti-angiogenic
drugs and chemotherapy are aimed at different cellular targets,
it is possible that the combination will prove even more effective
than either therapy is as a stand-alone.
Currently, Neovastat is the subject of three clinical trials,
targeting three forms of cancer for which there are urgent needs
for new therapies. For multiple myeloma, the second most common
form of blood cancer, the drug is in phase two trials with 125
patients in the United States, Canada and Europe. This trial should
be completed by the end of 2002. For progressive renal cell carcinoma,
the drug is in phase three trials with 280 patients in the United
States, Canada and Europe, which should be completed in early
2003. For non-small cell lung cancer, Neovastat is in a phase
three trial sponsored by the National Cancer Institute with 760
patients in the United States and Canada. This trial should be
completed in 2005.
Once the clinical trials are complete, health authorities in
various countries can then assess test results and make decisions
on approval.
Neovastat is being developed by Aeterna Laboratories of Quebec,
Canada. For more information about current trials, call (888)
349-3232. If you are an oncologist, contact Claude Hariton, PhD,
vice president of Clinical and Regulatory Affairs, (418) 652-8525,
Ext. 306.
To learn more about anti-angiogenesis and Aeterna Laboratories,
visit the Aeterna Web site at www.aeterna.com. For more information
about the NCI's clinical trials, visit http://cancertrials.nci.nih.gov.
About The Author - Courtesy ARA Content, www.ARAcontent.com;
e-mail: info@ARAcontent.com
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