Targeting angiogenesis in melanoma: prospects for the future

Angiogenesis has been identified as a relevant target for melanoma experimental therapeutics, based on preclinical and clinical studies. A variety of angiogenesis inhibitors are currently being tested in both metastatic and adjuvant melanoma clinical trials. To date, the most promising evidence of b...

Full description

Bibliographic Details
Main Authors: P.G. Corrie, B. Basu, K. Ahmad Zaki
Format: Article
Language:English
Published: SAGE Publishing 2010-11-01
Series:Therapeutic Advances in Medical Oncology
Online Access:https://doi.org/10.1177/1758834010380101
id doaj-ffacacbe565441c689f0d36c79893b4a
record_format Article
spelling doaj-ffacacbe565441c689f0d36c79893b4a2020-11-25T03:00:05ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83402010-11-01210.1177/1758834010380101Targeting angiogenesis in melanoma: prospects for the futureP.G. CorrieB. BasuK. Ahmad ZakiAngiogenesis has been identified as a relevant target for melanoma experimental therapeutics, based on preclinical and clinical studies. A variety of angiogenesis inhibitors are currently being tested in both metastatic and adjuvant melanoma clinical trials. To date, the most promising evidence of benefit is based on a statistically nonsignificant trend in survival gain reported in a randomized phase II trial combining bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, with cytotoxic chemotherapy. Larger phase III studies are required to determine the true extent of clinical benefit with this class of agents. Key to these clinical trials is the need to include translational endpoints, since correlation of biological and clinical data will provide the opportunity to identify biomarkers predictive of treatment response. These biological studies will also aid our, as yet, poor understanding of the mechanism of action of angiogenesis inhibitors, as well as drug-related side effects. Finally, if these trials show meaningful clinical benefit, then careful consideration will need to be given when designing second-generation trials, in the light of novel gene-directed therapies currently showing promise in melanoma.https://doi.org/10.1177/1758834010380101
collection DOAJ
language English
format Article
sources DOAJ
author P.G. Corrie
B. Basu
K. Ahmad Zaki
spellingShingle P.G. Corrie
B. Basu
K. Ahmad Zaki
Targeting angiogenesis in melanoma: prospects for the future
Therapeutic Advances in Medical Oncology
author_facet P.G. Corrie
B. Basu
K. Ahmad Zaki
author_sort P.G. Corrie
title Targeting angiogenesis in melanoma: prospects for the future
title_short Targeting angiogenesis in melanoma: prospects for the future
title_full Targeting angiogenesis in melanoma: prospects for the future
title_fullStr Targeting angiogenesis in melanoma: prospects for the future
title_full_unstemmed Targeting angiogenesis in melanoma: prospects for the future
title_sort targeting angiogenesis in melanoma: prospects for the future
publisher SAGE Publishing
series Therapeutic Advances in Medical Oncology
issn 1758-8340
publishDate 2010-11-01
description Angiogenesis has been identified as a relevant target for melanoma experimental therapeutics, based on preclinical and clinical studies. A variety of angiogenesis inhibitors are currently being tested in both metastatic and adjuvant melanoma clinical trials. To date, the most promising evidence of benefit is based on a statistically nonsignificant trend in survival gain reported in a randomized phase II trial combining bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, with cytotoxic chemotherapy. Larger phase III studies are required to determine the true extent of clinical benefit with this class of agents. Key to these clinical trials is the need to include translational endpoints, since correlation of biological and clinical data will provide the opportunity to identify biomarkers predictive of treatment response. These biological studies will also aid our, as yet, poor understanding of the mechanism of action of angiogenesis inhibitors, as well as drug-related side effects. Finally, if these trials show meaningful clinical benefit, then careful consideration will need to be given when designing second-generation trials, in the light of novel gene-directed therapies currently showing promise in melanoma.
url https://doi.org/10.1177/1758834010380101
work_keys_str_mv AT pgcorrie targetingangiogenesisinmelanomaprospectsforthefuture
AT bbasu targetingangiogenesisinmelanomaprospectsforthefuture
AT kahmadzaki targetingangiogenesisinmelanomaprospectsforthefuture
_version_ 1724699490389065728