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Updated: Mar 14, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Eribulin in the management of inoperable soft-tissue sarcoma: patient selection and survival
1Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA.
Abstract:
Patients diagnosed with metastatic soft-tissue sarcoma (STS) have a poor prognosis. Additionally, after failure of first-line therapy, there are relatively few treatment options from which to choose. The novel tubulin-binding drug, eribulin, with a unique mechanism of action from taxanes or vinca alkaloids, has shown clinical activity in several different types of cancers. Eribulin has been approved by the US Food and Drug Administration (FDA) for patients with metastatic breast cancer previously treated with an anthracycline or a taxane and has recently been FDA approved for patients with unresectable or metastatic liposarcoma who have failed a previous anthracycline regimen. Here, we review current standard treatments of STS, a background of eribulin, the studies that have propelled eribulin to FDA approval for liposarcoma, and future directions of the drug. The benefits of eribulin in STS are discussed in detail, especially with regard to the recent pivotal Phase III study comparing eribulin to dacarbazine for leiomyosarcoma and adipocytic sarcoma.
Insights
Eribulin offers a new treatment option for metastatic soft-tissue sarcoma (STS) patients who have not responded to initial therapies. This review details eribulin
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic soft-tissue sarcoma (STS) presents a poor prognosis with limited post-first-line therapy options.
- Eribulin, a novel tubulin-binding agent, demonstrates clinical activity across various cancers.
- Eribulin is FDA-approved for metastatic breast cancer and unresectable/metastatic liposarcoma.
Purpose of the Study:
- To review current standard treatments for STS.
- To provide background on eribulin's mechanism and clinical activity.
- To discuss studies leading to eribulin's FDA approval for liposarcoma and its benefits in STS.
Main Methods:
- Review of existing literature on STS treatments.
- Analysis of eribulin's pharmacological profile and mechanism of action.
- Examination of pivotal clinical trials, including a Phase III study comparing eribulin to dacarbazine.
Main Results:
- Eribulin has shown clinical activity in various cancers, including specific subtypes of STS.
- FDA approval for liposarcoma signifies eribulin's efficacy in a subset of STS patients.
- A Phase III study provides comparative data on eribulin versus dacarbazine for leiomyosarcoma and adipocytic sarcoma.
Conclusions:
- Eribulin represents a significant advancement in the treatment of metastatic STS.
- Further investigation into eribulin's role in STS is warranted.
- The drug offers a valuable therapeutic option for patients with advanced STS.
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