Efficacy of eribulin in patients (pts) with metastatic breast cancer (MBC): A pooled analysis by HER2 and ER status.

Authors

null

Chris Twelves

Leeds Institute of Cancer and Pathology, and St James's Institute of Oncology, Leeds, United Kingdom

Chris Twelves , Javier Cortes , Linda T. Vahdat , Martin S. Olivo , Yi He , Peter Andrew Kaufman , Ahmad Awada

Organizations

Leeds Institute of Cancer and Pathology, and St James's Institute of Oncology, Leeds, United Kingdom, University Hospital Vall d'Hebron, Barcelona, Spain, Weill Cornell Medical College, New York, NY, Eisai, Woodcliff Lake, NJ, Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center, Lebanon, NH, Institut Jules Bordet – Université Libre de Bruxelles, Brussels, Belgium

Research Funding

Pharmaceutical/Biotech Company

Background: Eribulin (E) has been assessed in 2 phase 3, open-label trials in pts with locally recurrent or MBC progressing after an anthracycline (A) and taxane (T). E significantly increased overall survival (OS) compared with treatment of physician’s choice (TPC) in 1 study and there was a non-significant trend for improved OS with E vs capecitabine (cape) in the other. We present an unplanned pooled analysis of these data. Methods: In the EMBRACE trial, women had received 2-5 lines of chemotherapy for advanced disease. In this ≥ third-line setting, pts were randomized 2:1 to E mesylate (1.4 mg/m2 iv on days 1 and 8 every 21 days) or TPC. In study 301, pts who had received 0–2 prior chemotherapies for advanced disease were randomized 1:1 to either E (as above) or cape (1.25 g/m2orally b.i.d. days 1–14 every 21 days). We analysed OS by 2-sided stratified log-rank tests and Cox regression in the overall intent-to-treat population and in the HER2–, triple negative (TNBC) and HER2+ subgroups. Results: In total 1,864 pts (median age 54 yrs) were included, most treated in the second (31.5%) or third-line (32.7%) MBC settings. Overall, E provided significantly improved OS vs control; this benefit was also significant in HER2− and TNBC, but not HER2+ pts (Table). E improved progression-free survival overall (4.0 vs 3.4 months, HR = 0.90, 95%CI = 0.81, 0.997, p = 0.046), in HER2– (3.7 vs 3.0 months, HR = 0.84, 95%CI = 0.74, 0.95, p = 0.006) and TNBC pts (2.8 vs 2.6 months, HR = 0.78, 95%CI = 0.63, 0.96, p= 0.018). As reported before, the E safety profile was similar in the studies. Conclusions: E significantly improved OS vs standard therapies in MBC pts with HER2− and TNBC in this pooled analysis; in pts with HER2+ disease the difference did not reach statistical significance but numbers were smaller. Clinical trial information: NCT00337103 and NCT00388726.

Overall
HER2−
HER2+
TNBC
E Con E Con E Con E Con
n 1062 802 748 572 169 123 243 185
Median OSa, months 15.2 12.8 15.2 12.3 13.5 12.2 12.9 8.2
HR (95%CI)b 0.85 (0.77, 0.95) 0.82 (0.72, 0.93) 0.82 (0.62, 1.06) 0.74 (0.60, 0.92)
pb 0.003 0.002 0.135 0.006

Abbreviations: Con, control; E, eribulin; HR, hazard ratio. aBased on survival curve adjusted by study. bStratified by geographic region, prior cape use and study (plus HER2 status for overall group only; plus TNBC for HER2– group only).

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Abstract Details

Meeting

2014 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer - HER2/ER

Track

Breast Cancer

Sub Track

HER2+

Clinical Trial Registration Number

NCT00337103 and NCT00388726

Citation

J Clin Oncol 32:5s, 2014 (suppl; abstr 631^)

DOI

10.1200/jco.2014.32.15_suppl.631

Abstract #

631^

Poster Bd #

95

Abstract Disclosures