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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

机译:聚乙二醇干扰素α-2b的辅助治疗与单独治疗III期黑色素瘤的观察:EORTC 18991的最终结果(一项随机III期试验)

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摘要

BACKGROUND: 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. METHODS: 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. FINDINGS: 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. INTERPRETATION: Adjuvant pegylated interferon alfa-2b for stage III melanoma has a significant, sustained effect on recurrence-free survival.
机译:背景:辅助干扰素α-2b对黑色素瘤的任何益处可能取决于治疗的剂量和持续时间。我们的目的是确定聚乙二醇化干扰素α-2b是否可以在维持耐受性的同时促进长时间暴露。方法:将1256例III期黑色素瘤切除患者随机分为观察组(n = 629)或聚乙二醇干扰素alfa-2b(n = 627),每周6杯/千克,持续8周(诱导),然后每周3杯/千克(维护),预期期限为5年。微观(N1)与宏观(N2)淋巴结受累,阳性淋巴结数目,溃疡和肿瘤厚度,性别和中心被随机化。用最小化技术进行随机化。主要终点是无复发生存期。分析是按意向进行的。该研究已在ClinicalTrials.gov上注册,编号为NCT00006249。结果:所有随机分组的患者均被纳入主要疗效分析。安全性分析包括干扰素组608例和观察组613例。聚乙二醇化干扰素α-2b治疗的中位时间为12(IQR 3.8-33.4)个月。在中位随访3.8(3.2-4.2)年,干扰素组发生了328例复发事件,而观察组发生了368例复发事件(危险比0.82,95%CI 0.71-0.96; p = 0.01)。干扰素组的4年无复发生存率为45.6%(SE 2.2),观察组为38.9%(2.2)。两组之间的总体生存率没有差异。干扰素组246例(40%)患者发生3级不良反应,观察组60例(10%)发生3级不良反应。干扰素组32例(5%)患者发生了4级不良事件,观察组14例(2%)发生了4级不良事件。在干扰素组中,最常见的3或4级不良反应是疲劳(97例,16%),肝毒性(66%,11%)和抑郁(39%,6%)。由于191名(31%)患者的毒性,终止了聚乙二醇化干扰素α-2b的治疗。解释:聚乙二醇化干扰素α-2b用于III期黑色素瘤的辅助治疗对无复发生存具有显着,持续的影响。

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