Eribulin mesylate

(Halaven®)

Eribulin mesylate

Drug updated on 11/5/2024

Dosage FormInjection (intravenous; 1 mg per 2 mL [0.5 mg per mL])
Drug ClassMicrotubule inhibitors
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of patients with metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease
  • Prior therapy should have included an anthracycline and a taxane in either the
  • adjuvant or metastatic setting
  • Indicated for the treatment of patients with unresectable or metastatic liposarcoma who have received a prior anthracycline-containing regimen.

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Summary
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  • This summary is based on the review of two systematic review(s)/meta-analysis(es). [1-2]
  • Locally Advanced/Metastatic Breast Cancer: In a network meta-analysis, eribulin mesylate (ERI) demonstrated improved overall survival (OS) compared to treatment by physician's choice (TPC) (HR (hazard ratio): 0.81; CrI: 0.66-0.99) and GEM+VIN (HR: 0.62; CrI: 0.42-0.90). ERI provided a longer progression-free survival (PFS) than TPC (HR: 0.76; CrI: 0.64-0.90) but was less effective than CAP+IXA (HR: 1.40; CrI: 1.17-1.67) and CAP+UTI (HR: 1.61; CrI: 1.23-2.12).
  • Triple Negative Breast Cancer (TNBC) Subgroup: In TNBC patients, ERI showed a statistically significant improvement in OS compared to CAP (HR: 0.70; CrI: 0.54-0.90), while there were no significant differences in PFS.
  • Older Patients with Breast Cancer (≥70 years): In a pooled analysis, older patients treated with ERI had a median OS of 13.1 months, a median PFS of 4.8 months, and a pooled overall response rate (ORR) of 23.2%, with a disease control rate (DCR) of 47%.
  • In older patients with breast cancer (pooled analysis), Grade 3-4 hematological toxicities included neutropenia (0-49%), with anemia and thrombocytopenia reported as rare; non-hematological toxicities included Grade 3-4 fatigue (5-16.5%) and neurotoxicity (0-10.1%). Dose reductions were necessary in 40% of patients (range 18.6-84%).
  • There are no direct safety comparisons between eribulin mesylate (ERI) and other drugs (CAP, GEM, IXA, UTI, TPC, VIN) in the reviewed studies.
  • There is no population types or subgroups information available in the reviewed studies.

Product Monograph / Prescribing Information

Document TitleYearSource
Halaven (eribulin mesylate) Prescribing Information.2022Eisai Inc., Nutley, NJ

Systematic Reviews / Meta-Analyses

Clinical Practice Guidelines

Document TitleYearSource
Systemic anti-cancer therapy delivery in the home: a service model.2020British Journal of Nursing