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PMID: 18620949 Published · ppublish English Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Adjuvant therapy with pegylated interferon alfa-2b versus observation alone in resected stage III melanoma: final results of EORTC 18991, a randomised phase III trial.

Lancet (London, England) ·Vol. 372 ·No. 9633 ·2008-07-12 ·Pages 117-126

Eggermont AM, Suciu S, Santinami M, Testori A, Kruit WH, Marsden J, Punt CJ, Salès F, Gore M, MacKie R, Kusic Z, Dummer R, Hauschild A, Musat E, Spatz A, Keilholz U, EORTC Melanoma Group

Abstract

Any benefit of adjuvant interferon alfa-2b for melanoma could depend on dose and duration of treatment. Our aim was to determine whether pegylated interferon alfa-2b can facilitate prolonged exposure while maintaining tolerability. 1256 patients with resected stage III melanoma were randomly assigned to observation (n=629) or pegylated interferon alfa-2b (n=627) 6 mug/kg per week for 8 weeks (induction) then 3 mug/kg per week (maintenance) for an intended duration of 5 years. Randomisation was stratified for microscopic (N1) versus macroscopic (N2) nodal involvement, number of positive nodes, ulceration and tumour thickness, sex, and centre. Randomisation was done with a minimisation technique. The primary endpoint was recurrence-free survival. Analyses were done by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00006249. All randomised patients were included in the primary efficacy analysis. 608 patients in the interferon group and 613 patients in the observation group were included in safety analyses. The median length of treatment with pegylated interferon alfa-2b was 12 (IQR 3.8-33.4) months. At 3.8 (3.2-4.2) years median follow-up, 328 recurrence events had occurred in the interferon group compared with 368 in the observation group (hazard ratio 0.82, 95% CI 0.71-0.96; p=0.01); the 4-year rate of recurrence-free survival was 45.6% (SE 2.2) in the interferon group and 38.9% (2.2) in the observation group. There was no difference in overall survival between the groups. Grade 3 adverse events occurred in 246 (40%) patients in the interferon group and 60 (10%) in the observation group; grade 4 adverse events occurred in 32 (5%) patients in the interferon group and 14 (2%) in the observation group. In the interferon group, the most common grade 3 or 4 adverse events were fatigue (97 patients, 16%), hepatotoxicity (66, 11%), and depression (39, 6%). Treatment with pegylated interferon alfa-2b was discontinued because of toxicity in 191 (31%) patients. Adjuvant pegylated interferon alfa-2b for stage III melanoma has a significant, sustained effect on recurrence-free survival.

MeSH Terms
Adolescent Adult Aged Antiviral Agents/adverse effects,therapeutic use Chemotherapy, Adjuvant Disease-Free Survival Female Humans Interferon alpha-2 Interferon-alpha/adverse effects,therapeutic use Male Melanoma/drug therapy,pathology,surgery Middle Aged Neoplasm Metastasis Observation Polyethylene Glycols Proportional Hazards Models Recombinant Proteins
Chemicals
Antiviral Agents Interferon alpha-2 Interferon-alpha Recombinant Proteins Polyethylene Glycols peginterferon alfa-2b
Authors & Affiliations
17 authors, click to expand affiliations / ORCID
Eggermont Alexander Mm
Erasmus University Medical Center, Rotterdam, Netherlands. Electronic address: a.m.m.eggermont@erasmusmc.nl.
Suciu Stefan
EORTC Headquarters, Brussels, Belgium.
Santinami Mario
Istituto Nazionale dei Tumori, Milan, Italy.
Testori Alessandro
Istituto Europeo di Oncologia, Milan, Italy.
Kruit Wim Hj
Erasmus University Medical Center, Rotterdam, Netherlands.
Marsden Jeremy
University Hospital Birmingham, Birmingham, UK.
Punt Cornelis Ja
University Medical Center St Radboud, Nijmegen, Netherlands.
Salès François
Institut Jules Bordet, Brussels, Belgium.
Gore Martin
Royal Marsden Hospital NHS, London, UK.
MacKie Rona
University of Glasgow, Glasgow, UK.
Kusic Zvonko
University Hospital Sestre Milosrdnice, Zagreb, Croatia.
Dummer Reinhard
University Clinic Zürich, Zürich, Switzerland.
Hauschild Axel
University Hospital Kiel, Kiel, Germany.
Musat Elena
EORTC Headquarters, Brussels, Belgium.
Spatz Alain
Institut Gustave-Roussy, Villejuif, France.
Keilholz Ulrich
Charité, Benjamin Franklin Campus, Berlin, Germany.
EORTC Melanoma Group
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
1474-547X
Published
2008-07-12
Pages
117-126
Language
English
Region
England
NLM ID
2985213R
Subset
IM
Databases
ClinicalTrials.gov
NCT00006249
Corrections
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