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Making Cancer More TreatableA Commitment to More Effective Cancer Treatments and Cancer Drugs
As CTI's cancer drugs progress through clinical
trials to commercialization,
our commitment to patients and the real issues of their cancer treatments
grows stronger. The challenge to overcome the therapeutic limitations of
cancer treatment provides us with a focus and sense of urgency.
Targeting the Side Effects and Toxicities of Conventional Cancer Therapies
Today, more than 9.2 million Americans have cancer, and one in three
people in North America and Europe will develop cancer
at some point in their lifetime. At the time of diagnosis,
70 percent of patients have tumors that have already
spread to other parts of their body. So, almost all receive
systemic therapy such as chemotherapy during the course
of their disease.
Despite recent advances in sequencing the human
genome and the introduction of new biologic therapies
for the treatment of cancer, almost all patients with
advanced cancer will receive chemotherapy at some point
during the treatment of their disease. Four classes of
chemotherapy agents — anthracyclines, camptothecins, platinates,
and taxanes — account for more than 95% of all chemotherapy
cancer drug usage. Unfortunately, there are significant
limitations and complications associated with these
agents that result in a high rate of treatment failure.
The principal limitations of chemotherapy in treating
cancer include:
- Treatment related toxicities
- Inability to selectively target tumor tissue
- The development of resistance to the cancer-killing effects of
chemotherapy
Overcoming the Limitations of Current Cancer Treatment
We believe next generation cancer treatment agents that
have lower toxicity and/or increased effectiveness than
these cornerstone chemotherapy classes address a significant
unmet need for the majority of cancer patients in the
U.S. and Europe. Our cancer drug development pipeline includes
a next generation drug candidate for each of the four leading
classes of chemotherapy agents.
We presently have
two products in late-stage clinical developmentXYOTAX and pixantrone,
and a robust product pipeline. Our capabilities span
drug development through commercialization.
Founded in 1991,
our headquarters is in Seattle, Washington with research
and development facilities in Seattle and Bresso (Milan),
Italy.
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Posted July 18, 2005
Copyright © 2004, 2005 Cell Therapeutics, Inc., Seattle,
WA, USA. All rights reserved. "Making cancer more treatable" is
a registered mark of CTI.
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