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dc.contributor.authorCojocaru, E
dc.contributor.authorThway, K
dc.contributor.authorFisher, C
dc.contributor.authorMessiou, C
dc.contributor.authorZaidi, S
dc.contributor.authorMiah, AB
dc.contributor.authorBenson, C
dc.contributor.authorGennatas, S
dc.contributor.authorHuang, P
dc.contributor.authorJones, RL
dc.date.accessioned2021-01-27T15:53:36Z
dc.date.issued2020-12-01
dc.identifier.citationAnticancer research, 2020, 40 (12), pp. 7003 - 7007
dc.identifier.issn0250-7005
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4320
dc.identifier.eissn1791-7530
dc.identifier.doi10.21873/anticanres.14725
dc.description.abstractBACKGROUND/AIM: Clear cell sarcoma (CCS) is an aggressive sarcoma subtype, resistant to conventional anthracycline-based chemotherapy and radiation. The diagnosis is often challenging due to similarities with malignant melanoma. PATIENTS AND METHODS: We aimed to analyse the activity of gemcitabine-based chemotherapy in a cohort of patients with CCS treated at the Royal Marsden Hospital. RESULTS: Five patients with metastatic CCS received gemcitabine as first- or second-line systemic therapy. The median time-to-progression was 10 weeks. The median number of cycles of gemcitabine-based therapy was 3 (range=2-7 cycles). Median overall survival in our cohort was 66 months from the initial diagnosis but in the metastatic setting, the overall survival was reduced to 28 months. CONCLUSION: Gemcitabine-based therapy has modest activity in CCS. There remains a significant unmet medical need for novel, effective therapies for this disease.
dc.formatPrint
dc.format.extent7003 - 7007
dc.languageeng
dc.language.isoeng
dc.publisherINT INST ANTICANCER RESEARCH
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.subjectHumans
dc.subjectSarcoma, Clear Cell
dc.subjectSoft Tissue Neoplasms
dc.subjectDeoxycytidine
dc.subjectAntimetabolites, Antineoplastic
dc.subjectAdult
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.titleEfficacy of Gemcitabine-based Chemotherapy in Clear Cell Sarcoma of Soft Tissue.
dc.typeJournal Article
dcterms.dateAccepted2020-11-08
rioxxterms.versionofrecord10.21873/anticanres.14725
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfAnticancer research
pubs.issue12
pubs.notesNot known
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.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
pubs.volume40
pubs.embargo.termsNot known
icr.researchteamMolecular and Systems Oncology
dc.contributor.icrauthorCojocaru, Elena
dc.contributor.icrauthorHuang, Paul


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