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Chemotherapeutics in Metastatic Breast Cancer

Panelists: Kimberly L. Blackwell, MD, Duke; Adam M. Brufsky, MD, PhD, University of Pittsburgh; Joyce A. O’Shaughnessy, MD, US Oncology; Mark D. Pegra
Published Online: Monday, Jun 09, 2014
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In January 2005, the FDA approved nab-paclitaxel (Abraxane) for the treatment of patients with metastatic breast cancer following progression on other chemotherapies. Since it’s approval, numerous studies have explored different dosing strategies with nab-paclitaxel, notes Hope S. Rugo, MD.

In the phase III CALGB 40502, nab-paclitaxel at 150 mg/m2 was compared to paclitaxel and ixabepilone. However, at doses of 150 mg/m2 the side effects were difficult to manage, remarks Rugo. Additionally, a clear subset of patients who benefited more from nab-paclitaxel was not identified. At this point the optimal dose remains 100 mg/m2, with studies ongoing that are looking at 125 mg/m2 doses, Rugo notes.

One of these studies (tnAcity) is evaluating the addition of nab-paclitaxel to gemcitabine and carboplatin as a treatment for patients with metastatic triple-negative breast cancer (TNBC), Denise A. Yardley, MD, notes. This phase II/III study plans to collect biomarkers and explore the risk—benefit ratio of the combination before moving onto the phase III portion of the study. Past research has suggested that Src may be a biomarker in select subtypes of TNBC; however, results from tnAcity remain to be seen, notes Yardley.

In 2010, the FDA approved eribulin mesylate (Halaven) for the treatment of patients with metastatic breast cancer following an anthracycline and a taxane. This approval was based on data from the phase III EMBRACE trial that demonstrated a statistically significant improvement in overall survival (OS) in patients receiving eribulin compared to physician's choice of treatment. In the study, the median OS was 13.1 months with eribulin versus 10.6 months in the control group.

Treatment with eribulin requires a 5-minute infusion, which is much shorter than other cytotoxic agents, notes Kimberly L. Blackwell, MD. Additionally, a phase III study demonstrated similar efficacy for eribulin and capecitabine in the first-, second, and third-line. Moreover, subgroup analyses from this trial suggest eribulin may be more active in patients with TNBC compared with capecitabine, Blackwell notes.

It is important to properly manage the side effects with eribulin, notes Rugo. As long as the neuropathy and neutropenia is controlled, the drug is very well tolerated. Additionally, Yardley notes, studies have explored this agent in combination with trastuzumab. These studies demonstrated promising results for the combination. 


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For High-Definition, Click
In January 2005, the FDA approved nab-paclitaxel (Abraxane) for the treatment of patients with metastatic breast cancer following progression on other chemotherapies. Since it’s approval, numerous studies have explored different dosing strategies with nab-paclitaxel, notes Hope S. Rugo, MD.

In the phase III CALGB 40502, nab-paclitaxel at 150 mg/m2 was compared to paclitaxel and ixabepilone. However, at doses of 150 mg/m2 the side effects were difficult to manage, remarks Rugo. Additionally, a clear subset of patients who benefited more from nab-paclitaxel was not identified. At this point the optimal dose remains 100 mg/m2, with studies ongoing that are looking at 125 mg/m2 doses, Rugo notes.

One of these studies (tnAcity) is evaluating the addition of nab-paclitaxel to gemcitabine and carboplatin as a treatment for patients with metastatic triple-negative breast cancer (TNBC), Denise A. Yardley, MD, notes. This phase II/III study plans to collect biomarkers and explore the risk—benefit ratio of the combination before moving onto the phase III portion of the study. Past research has suggested that Src may be a biomarker in select subtypes of TNBC; however, results from tnAcity remain to be seen, notes Yardley.

In 2010, the FDA approved eribulin mesylate (Halaven) for the treatment of patients with metastatic breast cancer following an anthracycline and a taxane. This approval was based on data from the phase III EMBRACE trial that demonstrated a statistically significant improvement in overall survival (OS) in patients receiving eribulin compared to physician's choice of treatment. In the study, the median OS was 13.1 months with eribulin versus 10.6 months in the control group.

Treatment with eribulin requires a 5-minute infusion, which is much shorter than other cytotoxic agents, notes Kimberly L. Blackwell, MD. Additionally, a phase III study demonstrated similar efficacy for eribulin and capecitabine in the first-, second, and third-line. Moreover, subgroup analyses from this trial suggest eribulin may be more active in patients with TNBC compared with capecitabine, Blackwell notes.

It is important to properly manage the side effects with eribulin, notes Rugo. As long as the neuropathy and neutropenia is controlled, the drug is very well tolerated. Additionally, Yardley notes, studies have explored this agent in combination with trastuzumab. These studies demonstrated promising results for the combination. 
View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Oncology Consultations®: Integrating Molecular Testing into the Breast Cancer Treatment ParadigmSep 28, 20162.0
Community Practice Connections™: 14th Annual International Congress on the Future of Breast Cancer®Oct 01, 20162.0
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