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Erschienen in: Journal of Cancer Research and Clinical Oncology 2/2009

01.02.2009 | Letter to the Editor

Control of aggressive fibromatosis by treatment with imatinib mesylate: a step forward?

verfasst von: Alberto Ravaioli, Stefania Nicoletti, Emiliano Tamburini, Maximilian Papi

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 2/2009

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Abstract

Numerous studies referring to conventional chemotherapy for aggressive fibromatosis with the use of doxorubicin, cyclophosphamide, vincristin, vinblastine and other drugs have been published. Imatinib mesylate is a recently developed oral anticancer agent designed to selectively inhibit tyrosine kinases implicated in oncogenesis and it seems to represent a promising opportunity (also in first line) in the treatment of patients with advanced disease not candidate to prior surgery.
Literatur
Zurück zum Zitat Demetri GD, von Mahren M, Blanke CD et al (2002) Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors. N Engl J Med 346:472–480. doi:10.1056/NEJMoa020461 CrossRef Demetri GD, von Mahren M, Blanke CD et al (2002) Efficacy and safety of imatinib mesylate in advanced gastrointestinal stromal tumors. N Engl J Med 346:472–480. doi:10.​1056/​NEJMoa020461 CrossRef
Zurück zum Zitat Wcislo G, Szarlej-Wcislo K, Szczylik C (2007) Control of aggressive fibromatosis by treatment with imatinib mesylate. A case report and review of the literature. J Cancer Res Clin Oncol 133:533–538. doi:10.1007/s00432-007-0198-9 PubMedCrossRef Wcislo G, Szarlej-Wcislo K, Szczylik C (2007) Control of aggressive fibromatosis by treatment with imatinib mesylate. A case report and review of the literature. J Cancer Res Clin Oncol 133:533–538. doi:10.​1007/​s00432-007-0198-9 PubMedCrossRef
Metadaten
Titel
Control of aggressive fibromatosis by treatment with imatinib mesylate: a step forward?
verfasst von
Alberto Ravaioli
Stefania Nicoletti
Emiliano Tamburini
Maximilian Papi
Publikationsdatum
01.02.2009
Verlag
Springer-Verlag
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 2/2009
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-008-0459-2

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