Metastatic Breast Cancer Clinical Trial
Official title:
Phase II Study of Ixabepilone in Patients With Metastatic Breast Cancer and a Prospective Evaluation of Its Effects on the Ultrastructure of Neurons
Primary Objectives
- Assess ultrastructure changes in dermal myelinated nerves of patients who receive
ixabepilone chemotherapy
- Detailed characterization of peripheral neuropathy in patients who receive ixabepilone
Secondary Objectives
- Clinical benefit rate
- Time to progression ( TTP)
- Toxicity
- Exploratory studies:
- Relation of MDR 1 and TRKA polymorphisms to evolution of ultrastructural neurologic
changes observed in neurons.
- Relation of NGF, IL8, and IL10 to the development of clinical symptoms and
ultrastructural changes in neurons.
Eligible patient population:
- Stage 4 breast cancer
- Resolution from toxicity of prior therapy to ≤ CTC grade 1 ( except alopecia)
- No limit on prior number of therapies to treat cancer
- Adequate organ function
- Life expectancy greater than 3 months
Treatment: ixabepilone 40 mg/m2 Q3w over 3 hours
Evaluation on Study:
I. Efficacy evaluation:
- Baseline CT chest, abdomen and pelvis and bone scan within 4 weeks of starting therapy
- Evaluation of disease every 2 cycles of chemotherapy
- Ongoing toxicity evaluation using NCI CTC 3.
II. Neurological evaluation:
- Detailed neurologic exam using Neuropathy Assessment Instrument (represents a standard
neurological exam)
- Serum NGF, IL 8,10, prior to starting therapy and prior to each cycle of ixabepilone
- DNA for assessment of TRK A and MDR1 polymorphisms
- Punch biopsy of skin prior to starting therapy and after every 2 cycles. Laboratory
evaluation of peripheral nerve biopsies will be conducted at Rockefeller University
under the direction of Dr. Carlson in Dr. Strickland's Lab.
;
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