Literature DB >> 23665062

A review of contemporary options for medical management of hemangiomas, other vascular tumors, and vascular malformations.

Julie Blatt1, Thomas W McLean, Sharon M Castellino, Craig N Burkhart.   

Abstract

Vascular anomalies include vascular tumors and vascular malformations. With growing pharmacologic options and parallels to cancer treatment and biology, the hematologist-oncologist has assumed a more prominent role in clinical care and research relating to these diagnoses. This also is a growing area for targeted therapies and drug repositioning. We performed a review of contemporary options for medical management of these lesions. PubMed was searched for "vascular anomaly", "hemangioma", "vascular malformation", "arteriovenous malformation", "capillary malformation", "cerebral cavernous malformation", "lymphatic malformation", and "venous malformation", each with "drug treatment" as a modifier. Manuscripts were reviewed to verify diagnoses, indications for treatment, dose-schedules, evidence of effectiveness, toxicities, and mechanisms of action. ClinicalTrials.gov also was reviewed for relevant trials. More than 20 agents were identified which have been used to treat vascular anomalies. Rigorous studies are lacking for many of these. The rarity of these tumors has limited development of medical approaches to treatment. Cooperative group trials will be needed to prove the effectiveness of drugs which have shown promise in cases and small series. The observant clinician remains a powerful tool for identifying potential new treatments for vascular tumors and malformations.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  <5 cases demonstrating efficacy; AVM; C; CCM; CM; Drug treatment; FGF; HHT; Hemangioma; IH; KMS; Kasabach–Merritt syndrome; LM; MMP; R; S; VEGF; VM; Vascular anomaly; Vascular malformation; arteriovenous malformation; capillary malformation; cerebral cavernous malformation; fibroblast growth factor; hemangioma of infancy; hereditary hemorrhagic telangiectasia; lymphatic malformation; mTOR; mammalian target of rapamycin; matrix metalloproteinase; randomized clinical trial; retrospective series≥5 cases demonstrating efficacy; rs; single arm clinical trial; vascular endothelial growth factor; venous malformation

Mesh:

Year:  2013        PMID: 23665062     DOI: 10.1016/j.pharmthera.2013.05.001

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


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