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Orthotopic Transplantation of Breast Tumors as Preclinical Models for Breast Cancer
Published on: May 18, 2020
Application of epothilones in breast cancer therapy
1Northwestern University, Feinberg School of Medicine, Division of Hematology/Oncology, , Robert H. Lurie Comprehensive Cancer Center, Chicago, Illinois 60611, USA. m-cianfrocca@northwestern.edu
Purpose Of Review:
The taxanes that target microtubules are among the most active drugs in breast cancer treatment; however, resistance to these agents remains a significant issue for many patients. The epothilones are a novel class of nontaxane, microtubule-targeting agents, currently being evaluated in varying stages of clinical trials. Ixabepilone is the first epothilone analogue to receive US Food and Drug Administration approval in the United States for the treatment of metastatic breast cancer and as such will be the primary focus of this review.
Recent Findings:
Multiple phase II trials evaluating ixabepilone in different populations of patients with metastatic breast cancer as well as a phase III trial in combination with capecitabine have recently been published.
Summary:
Phase II trials clearly demonstrate the activity of single-agent ixabepilone in both taxane-untreated and taxane-treated metastatic breast cancer. Although the highest activity was seen in early lines of therapy, there was also clear evidence of activity in heavily pretreated patients. Ixabepilone has also been evaluated in combination with capecitabine in a randomized, phase III trial demonstrating a benefit for the combination compared with single-agent capecitabine for patients resistant to anthracyclines and taxanes. In general, ixabepilone administered as a single-agent and in combination with capecitabine has been reasonably well tolerated.
Insights
Ixabepilone shows effectiveness in treating metastatic breast cancer, even in patients resistant to other therapies. This novel microtubule-targeting agent offers a new option for breast cancer treatment.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Taxanes are key microtubule-targeting drugs for breast cancer but face resistance.
- Epothilones represent a novel class of microtubule-targeting agents.
- Ixabepilone is the first FDA-approved epothilone analogue for metastatic breast cancer.
Purpose of the Study:
- To review the clinical efficacy and safety of ixabepilone in metastatic breast cancer.
- To focus on ixabepilone as a novel therapeutic agent for breast cancer.
Main Methods:
- Review of multiple Phase II trials of ixabepilone in metastatic breast cancer.
- Analysis of a Phase III trial combining ixabepilone with capecitabine.
Main Results:
- Ixabepilone demonstrates activity as a single agent in both taxane-naive and taxane-resistant metastatic breast cancer.
- Activity was observed in early and heavily pretreated patient populations.
- Combination therapy with capecitabine showed benefit in anthracycline- and taxane-resistant patients.
- Ixabepilone was generally well-tolerated in single-agent and combination use.
Conclusions:
- Ixabepilone is an active agent in metastatic breast cancer, including in patients resistant to taxanes.
- Combination with capecitabine offers a therapeutic option for resistant disease.
- Ixabepilone presents a favorable safety profile in clinical trials.
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