Journal of Clinical Oncology, Vol 23, No 6 (February 20), 2005: pp. 1295-1311
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.10.022
Combination of Antiangiogenic Therapy With Other Anticancer Therapies: Results, Challenges, and Open Questions
Giampietro Gasparini,
Raffaele Longo,
Massimo Fanelli,
Beverly A. Teicher
From the Division of Medical Oncology, S. Filippo Neri Hospital, Rome, Italy; and Genzyme Corporation, Framingham, MA
Address reprint requests to Giampietro Gasparini, MD, Division of Medical Oncology, Azienda Complesso Ospedaliero S. Filippo Neri, Via C. Martinotti, 20 00135 Rome, Italy; e-mail: gasparini.oncology{at}tiscalinet.it
Angiogenesis is necessary for tumor growth. Drug discovery efforts have identified several potential therapeutic targets on endothelial cells and selective inhibitors capable of slowing tumor growth or producing tumor regression by blocking angiogenesis in in vivo tumor models. Certain antiangiogenic therapeutics increase the activity of cytotoxic anticancer treatments in preclinical models. More than 75 antiangiogenic compounds have entered clinical trials. Most of the early clinical testing was conducted in patients with advanced disease resistant to standard therapies. Several phase III trials have been undertaken to compare the efficacy of standard chemotherapy versus the same in combination with an experimental angiogenesis inhibitor. Preliminary results of the clinical studies suggest that single-agent antiangiogenic therapy is poorly active in advanced tumors. Although some of the results of combination trials are controversial, recent positive outcomes with an antivascular endothelial growth factor antibody combined with chemotherapy as front-line therapy of metastatic colorectal cancer have renewed enthusiasm for this therapeutic strategy. This article presents an overview of experimental and clinical studies of combined therapy with antiangiogenic agents and highlights the challenges related to the appropriate strategies for selection of the patients, study design, and choice of proper end points for preclinical and clinical studies using these agents.
Authors' disclosures of potential conflicts of interest are found at the end of this article.
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