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Phase 3 Trial of Ixabepilone Combo Shows Improved Progression-Free Survival in Patients with Breast Cancer
"Patients whose disease is no longer responding to currently approved chemotherapies have few proven treatment options available to them," said Renzo Canetta, Vice President, Oncology Global Clinical Research, Bristol-Myers Squibb. "The results of this study provide important information about this investigational compound especially for patients with metastatic breast cancer resistant to anthracyclines and taxanes."
In this international open-label Phase III trial, 752 patients with metastatic breast cancer whose disease had rapidly progressed through at least two prior therapies (anthracycline and taxane), were randomly assigned to receive ixabepilone in combination with capecitabine or capecitabine alone. Study results showed that ixabepilone in combination with capecitabine:
- Prolonged progression-free survival (5.8 months vs. 4.2 months) - with a statistically significant 25 percent decrease in the risk of disease progression (Hazard ratio, 0.75; 95.17% CI = 3.81- 4.50; p Resulted in an objective response rate in more than twice as many patients (35% vs. 14%).
For ixabepilone in combination with capecitabine, most treatment-related adverse events were consistent with the safety profile of the individual agents. In addition, capecitabine-associated toxicities (such as hand-foot syndrome) were not exacerbated by ixabepilone.
Treatment-related non-hematologic Grade 3/4 adverse events reported in patients treated with ixabepilone in combination with capecitabine included: peripheral neuropathy (23%), hand-foot syndrome (18%), fatigue (9%), myalgia (8%), diarrhea (6%), vomiting (4%), nausea (3%), mucositis (3%), and arthralgia (3%). Treatment-related non-hematologic Grade 3/4 adverse events reported in patients treated with capecitabine alone included: hand-foot syndrome (17%), diarrhea (9%), fatigue (3%), vomiting (2%), nausea (2%), mucositis (2%), myalgia (0.3%), arthralgia (0%), and peripheral neuropathy (0%). Treatment-related hematological Grade 3/4 adverse events in patients treated with ixabepilone in combination with capecitabine included: leukopenia (57%), anemia (10%), neutropenia (68%), thrombocytopenia (8%), and febrile neutropenia (4%). Treatment-related hematological Grade 3/4 adverse events in patients treated with capecitabine only included: leukopenia (6%), anemia (4%), neutropenia (11%), thrombocytopenia (4%), and febrile neutropenia (
Ixabepilone, a semisynthetic analog of epothilone B, is an investigational compound. Epothilones and their analogs are a potential new class of antineoplastic, chemotherapy agents. For information on ixabepilone clinical trials, log on to www.clinicaltrials.gov.
Source: Bristol-Myers Squibb