Breast cancer patients failed by treatment with taxol and taxotere respond to abraxane

imen are impressive in this population of taxane-refractory patients," said Dr. Joanne Blum, Principal Investigator of the study. "Abraxane differentiates itself from other taxanes because it enables us to administer more cancer-fighting paclitaxel to the patient without an increase in side effects one might expect to see with currently available taxane therapies."

"It appears that Abraxane allows for more cancer-fighting drug to be given to a patient, more of that drug to actually reach the tumor site in the body, and more of the drug to get inside of the tumor to fight cancer cells."

The tolerability of the weekly regimen was demonstrated by the finding of <1 percent grade 4 febrile neutropenia and no grade 4 non-hematological toxicities. Grade 3 associated toxicities were few, with <4 percent sensory neuropathy, <3 percent fatigue, <1 percent edema, <1 percent tearing, and no Grade 3 nail changes, myalgia, arthralgia, hypersensitivity or flushing.

A New Drug Application for Abraxane is currently under review by the U.S. Food and Drug Administration. Abraxane is an investigational drug that uses nanoparticle technology to combine paclitaxel long been considered one of the most effective cancer drugs with the natural protein "transporter" albumin, avoiding the need for toxic solvents and detergents like those used in Taxol and Taxotere. By eliminating these toxic elements, patients treated with Abraxane do not typically need routine premedications.

The previously reported pivotal Phase III trial demonstrated superior response rate and time to tumor progression in metastatic breast cancer patients versus Taxol.


Contact: Melyssa Weible
HealthStar PR

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