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 https://cancertrials.nci.nih.gov .
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