Pfizer's Sutent improves survival in cancer study

Key points
- Pfizer Inc.'s experimental drug Sutent improved survival and reduced tumor growth in patients with a type of stomach cancer, according to a pivotal-stage trial the company unveiled this weekend.
- The study, the final one before the company seeks U.S.
- Results, presented here at a meeting of the American Society of Clinical Oncology, showed Sutent prolonged the time it took before tumors grew to 6.3 months from 1.5 months and improved survival by about 50 percent, compared to placebo.
- The world's biggest drugmaker said it planned to file for FDA review of the drug as a treatment for gastrointestinal Stromal tumors before the end of the year.
Pfizer Inc.'s experimental drug Sutent improved survival and reduced tumor growth in patients with a type of stomach cancer, according to a pivotal-stage trial the company unveiled this weekend.
The study, the final one before the company seeks U.S. Food and Drug Administration approval for the drug, involved 300 patients with gastrointestinal Stromal tumors whose cancer had become resistant to Gleevec (or Glivec), a drug sold by Novartis AG.
Results, presented here at a meeting of the American Society of Clinical Oncology, showed Sutent prolonged the time it took before tumors grew to 6.3 months from 1.5 months and improved survival by about 50 percent, compared to placebo.
The world's biggest drugmaker said it planned to file for FDA review of the drug as a treatment for gastrointestinal Stromal tumors before the end of the year.
The trial was stopped ahead of schedule in January after investigators said patients on placebo should be switched to Sutent, given the drug's demonstrated activity.
Sutent is designed to block biological switches involved in the growth of tumors and the blood vessels that support them.
Dr. William Slichenmyer, vice president of oncology drug development at Pfizer, said the company chose to first study the drug in the stomach cancer indication because patients have no other alternatives once they have stopped responding to Gleevec.
"This represents an extremely hopeful outcome for cancer patients ... by inhibiting these abnormal signals with new rationally designed drugs, we can offer patients the benefits of disease control and longer survival," the study's lead author Dr. George Demetri of Dana-Farber Cancer Institute in Boston, said in a statement.
About 75 percent to 80 percent of patients on Gleevec eventually become resistant to the drug, said Dr. Michael Heinrich, professor of medicine, hematology and medical oncology at Oregon Health and Science University in Portland.
"The big news is that this is an unmet medical need. Now there is at least one drug that appears to offer hope," he said. "We are starting to show a way in oncology to target cancer cells in different ways."
Still, Pfizer faces competition and its drug has an array of side effects that could limit its use in some patients. For one thing, it causes fatigue to the point that patients must take a two-week break after each four-week period of treatment to recover, the company said.
Sutent can also cause white blood cell counts to fall, making patients more susceptible to infection, and it can cause nausea and diarrhea.
Novartis is racing to develop a drug of its own - AMN107 - to treat patients who become resistant to Gleevec. A late-stage trial of the drug in patients with Gleevec-resistant leukemia-like disorders began recently.
Written and revised by
Gerald Hurowitz, M.D.
Our doctors write and review articles for accuracy and keep them up to date.
health.am provides general information, not medical advice. Always consult a qualified health professional about your own health.
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