TY - JOUR
T1 - Redefining the role of interferon in the treatment of malignant diseases
AU - Bracarda, Sergio
AU - Eggermont, Alexander M.M.
AU - Samuelsson, Jan
N1 - Funding Information:
Dr. Bracarda has served on advisory boards for Bayer Schering-Pharma, Pfizer, F. Hoffmann-La Roche Ltd., Wyeth, Novartis and GlaxoSmithKline and has received honoraria for lectures from Novartis. Dr. Eggermont is a consultant and holds a research grant for Schering Plough. Dr. Samuelsson is a consultant for Swedish Orphan pharmaceuticals, has received honoraria for lectures from F. Hoffmann-La Roche Ltd., and has served on advisory boards for F. Hoffmann-La Roche Ltd. and GlaxoSmithKline.
Funding Information:
The authors acknowledge the medical writing support of Stuart Langley of Gardiner-Caldwell Communications (Macclesfield, UK). The medical writing support was funded by F. Hoffmann-La Roche Ltd., Basel, Switzerland.
PY - 2010/1
Y1 - 2010/1
N2 - 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in cancer development and growth and the availability of effective, alternative therapies have led to IFN therapy being superseded in many cancers.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.
AB - 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.
KW - Angiogenesis
KW - Clinical trial
KW - Interferon
KW - Melanoma
KW - Myeloproliferative disorders
KW - Renal cell carcinoma
KW - Treatment protocols
UR - http://www.scopus.com/inward/record.url?scp=72449141577&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2009.10.013
DO - 10.1016/j.ejca.2009.10.013
M3 - Article
C2 - 19906524
AN - SCOPUS:72449141577
SN - 0959-8049
VL - 46
SP - 284
EP - 297
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 2
ER -