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Volume 46, Issue 2, Pages 284-297 (January 2010)


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Redefining the role of interferon in the treatment of malignant diseases

Sergio BracardaaCorresponding Author Informationemail address, Alexander M.M. Eggermontb, Jan Samuelssonc

Received 28 July 2009; received in revised form 18 September 2009; accepted 9 October 2009. published online 11 November 2009.

Abstract 

Interferon (IFN) is a cytokine with a long history of use as immunotherapy in the treatment of various solid tumours and haematological malignancies. The initial use of IFN in cancer therapy was based on its antiproliferative and immunomodulatory effects, and it has been shown more recently to have cytotoxic and anti-angiogenic properties. These features make it a rational anticancer therapy; however, advances in our understanding of the molecular mechanisms involved in cancer development and growth and the availability of effective, alternative therapies have led to IFN therapy being superseded in many cancers. IFN is still commonly used in renal cell carcinoma (RCC), melanoma and myeloproliferative disorders, in which its optimal dose and treatment duration remain to be established despite extensive clinical experience. Preclinical studies of the mechanism of action of IFN suggest that different antitumour effects are relevant at different doses, providing a rationale to explore the use of different dose regimens of IFN, particularly when combined with other therapies. In particular, the advent of novel anti-angiogenic therapies in RCC means that the role of IFN needs to be re-examined with a focus on how best to maximise efficacy and minimise toxicity when used with these agents. This review will focus on the therapeutic use of IFN in these disorders, provide an overview of available data and consider what the data suggest regarding the potential optimal use of IFN in the future.

a Department of Oncology and U.O.C. of Medical Oncology, Ospedale San Donato, Azienda USL-8, 52100 Arezzo, Italy

b Erasmus University MC – Daniel den Hoed Cancer Center, 3075 EA Rotterdam, The Netherlands

c Karolinska Institute, Department of Clinical Science and Education, Department of Internal Medicine, Stockholm South Hospital, 118 83 Stockholm, Sweden

Corresponding Author InformationCorresponding author: Address: Department of Oncology and U.O.C. of Medical Oncology, Ospedale San Donato, AUSL-8, Via Pietro Nenni, 20, 52100 Arezzo, Italy. Tel.: +39 0575 25 5439; fax: +39 0575 25 5435.

PII: S0959-8049(09)00760-6

doi:10.1016/j.ejca.2009.10.013


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