Show simple item record

dc.contributor.authorPhillips, E
dc.contributor.authorJones, RL
dc.contributor.authorHuang, P
dc.contributor.authorDigklia, A
dc.date.accessioned2022-04-13T08:46:37Z
dc.date.available2022-04-13T08:46:37Z
dc.date.issued2022-03-30
dc.identifier.citationFrontiers in Pharmacology, 13
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5078
dc.identifier.eissn1663-9812
dc.identifier.eissn1663-9812
dc.identifier.doi10.3389/fphar.2022.869754
dc.identifier.doi10.3389/fphar.2022.869754
dc.description.abstractSoft tissue sarcomas are a highly heterogenous group of tumors with limited systemic therapy options. Eribulin, a synthetic analogue of halichondrin B, is a potent mitotic inhibitor. A phase 3 trial of previously treated advanced Liposarcoma and Leiomyosarcoma demonstrated superiority of eribulin to dacarbazine. Eribulin appears to be particularly effective for liposarcomas. It has also been shown to be a safe and effective treatment alternative to doxorubicin in patients where doxorubicin is contraindicated. From retrospective studies, eribulin has demonstrated efficacy in patients with angiosarcoma, pleomorphic sarcomas, synovial sarcomas, rhabdomyosarcomas, angiosarcomas, and myxofibrosarcomas. Future areas of development include liposomal eribulin, which may provide increased efficacy and lower toxicity, and delineation of biomarkers of response and resistance, allowing better selection of patients for treatment.
dc.language.isoeng
dc.publisherFRONTIERS MEDIA SA
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleEfficacy of Eribulin in Soft Tissue Sarcomas.
dc.typeJournal Article
dcterms.dateAccepted2022-03-30
rioxxterms.versionVoR
rioxxterms.versionofrecord10.3389/fphar.2022.869754
dc.relation.isPartOfFrontiers in Pharmacology
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Molecular and Systems Oncology
pubs.publication-statusPublished online
pubs.volume13
pubs.embargo.termsNo embargo
icr.researchteamMolecular and Systems Oncology
dc.contributor.icrauthorHuang, Paul


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

http://creativecommons.org/licenses/by/4.0/
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/