Literature DB >> 20537949

Angiosarcoma.

Robin J Young1, Nicola J Brown, Malcolm W Reed, David Hughes, Penella J Woll.   

Abstract

Angiosarcomas are rare soft-tissue sarcomas of endothelial cell origin that have a poor prognosis. They can arise anywhere in the body, most commonly presenting as cutaneous disease in elderly white men, involving the head and neck and particularly the scalp. They can be caused by therapeutic radiation or chronic lymphoedema and hence secondary breast angiosarcomas are an important subgroup. Recent work has sought to establish the molecular biology of angiosarcomas and identify specific targets for treatment. Interest is now focused on trials of vascular-targeted drugs, which are showing promise in the control of angiosarcomas. In this review we discuss angiosarcoma and its current management, with a focus on clinical trials investigating the treatment of advanced disease.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20537949     DOI: 10.1016/S1470-2045(10)70023-1

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  274 in total

1.  Metastatic Cutaneous Angiosarcoma: A Rare Entity.

Authors:  Javier Blanco Jimenez; Ghulam Aftab; Dallis Q Ngo
Journal:  Cureus       Date:  2021-04-20

Review 2.  The horizon for treating cutaneous vascular lesions.

Authors:  Amit M Patel; Elizabeth L Chou; Laura Findeiss; Kristen M Kelly
Journal:  Semin Cutan Med Surg       Date:  2012-06

3.  A retrospective review of 145 patients with angiosarcoma: Radiation therapy, extent of resection and chemotherapy are important predictors of survival.

Authors:  Alannah Smrke; Jeremy Hamm; Anand Karvat; Christine Simmons; Amirrtha Srikanthan
Journal:  Mol Clin Oncol       Date:  2020-06-02

4.  Ovarian angiosarcoma: Extended survival following optimal cytoreductive surgery and adjuvant chemotherapy.

Authors:  Stephanie H Guseh; Leslie S Bradford; Lida P Hariri; John O Schorge
Journal:  Gynecol Oncol Case Rep       Date:  2012-12-20

Review 5.  Eyelid angiosarcoma: a case report and review of the literature.

Authors:  Hakan Demirci; Murray D Christanson
Journal:  Middle East Afr J Ophthalmol       Date:  2013 Jul-Sep

6.  Pharmacologic inhibition of MEK signaling prevents growth of canine hemangiosarcoma.

Authors:  Nicholas J Andersen; Brian J Nickoloff; Karl J Dykema; Elissa A Boguslawski; Roman I Krivochenitser; Roe E Froman; Michelle J Dawes; Laurence H Baker; Dafydd G Thomas; Debra A Kamstock; Barbara E Kitchell; Kyle A Furge; Nicholas S Duesbery
Journal:  Mol Cancer Ther       Date:  2013-06-26       Impact factor: 6.261

7.  Comprehensive treatment of unresectable cardiac angiosarcoma: A case report and review of literature.

Authors:  Chao Wang; Min Shi; Chen Yang; Tao Ma; Jinling Jiang; Ying Liu; Wenqi Xi; Zhenggang Zhu; Jun Zhang
Journal:  Mol Clin Oncol       Date:  2017-08-24

8.  Stewart-Treves syndrome: Magnetic resonance imaging data compared with pathological results from a single center.

Authors:  Bin Li; Zhenchang Wang
Journal:  Oncol Lett       Date:  2017-11-08       Impact factor: 2.967

9.  Clinical management of secondary angiosarcoma after breast conservation therapy.

Authors:  Martina Zemanova; Katarina Machalekova; Monika Sandorova; Elena Boljesikova; Marta Skultetyova; Juraj Svec; Andrej Zeman
Journal:  Rep Pract Oncol Radiother       Date:  2013-08-23

10.  Angiosarcoma outcomes and prognostic factors: a 25-year single institution experience.

Authors:  Darya Buehler; Stephanie R Rice; John S Moody; Patrick Rush; Gholam-Reza Hafez; Steven Attia; B Jack Longley; Kevin R Kozak
Journal:  Am J Clin Oncol       Date:  2014-10       Impact factor: 2.339

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