A Phase 2 Study of the Eribulin in Patients with Metastatic Angiosarcoma and Epithelioid Hemangioendothelioma (EHE).
case_series · Level IV
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- Record sourced from PubMed, PMID 41481257.
- Also identified by DOI 10.1158/1078-0432.CCR-25-3362.
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Abstract
Angiosarcoma and epithelioid hemangioendothelioma (EHE) are two rare vascular sarcomas with limited therapeutic options. Prior reports have shown sensitivity to microtubule-targeting agents in these histologies. We report the efficacy and safety of eribulin in these two vascular sarcomas in a pooled analysis of two parallel phase 2 studies. Patients over age 18 years with metastatic or recurrent angiosarcoma or EHE were treated with eribulin (1.4 mg/m2 on days 1 and 8 of a 21-day cycle) until progression or unacceptable toxicity. The primary endpoint was objective response rate by RECIST 1.1. 29 patients were accrued to the study, 25 (85%) having had prior taxane exposure. We observed an objective response rate (ORR) of 17% for angiosarcomas, with 6/23 (26%) patients achieving disease stability for greater than 6 months, and for EHE an ORR of 33% (2/6) with 2/6 continuing treatment for over 12 months. Five patients experienced a >1.3-fold time to progression ratio (TTP2/TTP1) on eribulin compared to the immediately prior therapy. Eribulin tolerability was consistent with published data. Eribulin showed clinical activity in this largely taxane-pretreated population. Future studies will be needed to confirm activity.