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Volume 46, Issue 1, Pages 41-46 (January 2010)


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Pegylated interferons: Prospects for the use in the adjuvant and palliative therapy of metastatic melanoma

Katharina C. KaehleraCorresponding Author Informationemail address, Vernon K. Sondakbcd, Dirk Schadendorfe, Axel Hauschilda

Received 15 July 2009; received in revised form 23 September 2009 published online 26 October 2009.

Abstract 

Classic interferon-α formulations have antitumour activity in a variety of neoplastic diseases, including the adjuvant and palliative setting of metastatic melanoma, as single agents or in combination with chemotherapy and/or interleukin-2. Pegylated interferon, widely used for the treatment of hepatitis, seems to be at least equally efficacious as standard recombinant interferon in the treatment of metastatic melanoma, and the available evidence suggests that equi-efficacious doses have somewhat lower acute toxicity. Moreover, the favourable pharmacokinetic properties of pegylated interferon allow the administration on a weekly basis, with sustained exposure to interferon during that entire period.

Several clinical trials have been conducted testing adjuvant and palliative treatment with pegylated interferon-α in high-risk melanoma patients with promising results. The role of pegylated interferons in the setting of advanced metastatic melanoma will need further investigation in clinical trials, potentially in combination with targeted or cytotoxic agents with regard to synergistic antiangiogenic and cytotoxic effects. The use of pegylated interferons in earlier stage melanomas will be investigated in upcoming trials.

a Department of Dermatology, University of Kiel, Kiel, Germany

b Department of Cutaneous Oncology, Moffitt Cancer Center, University of South Florida, Tampa, FL, USA

c Department of Oncologic Sciences, University of South Florida, Tampa, FL, USA

d Department of Surgery, University of South Florida, Tampa, FL, USA

e Department of Dermatology, University of Essen, Germany

Corresponding Author InformationCorresponding author: Tel.: +49 4315971512; fax: +49 4315971853.

PII: S0959-8049(09)00729-1

doi:10.1016/j.ejca.2009.10.004


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