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首页> 外文期刊>Annals of Hematology >Pilot study of pegylated interferon alpha-2a treatment during chemo- and radiotherapy and post-remission maintenance in patients with EBV-positive extranodal NK/T cell lymphoma
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Pilot study of pegylated interferon alpha-2a treatment during chemo- and radiotherapy and post-remission maintenance in patients with EBV-positive extranodal NK/T cell lymphoma

机译:聚乙二醇干扰素α-2a治疗EBV阳性结外NK / T细胞淋巴瘤患者的化学和放射治疗以及缓解后维持的初步研究

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摘要

The role of the Epstein–Barr virus (EBV) in the pathogenesis of extranodal natural killer/T-cell lymphoma (ENKTCL), and its resistance to chemotherapy raises the possibility of antiviral therapeutic strategies. The aim of this prospective pilot study was to evaluate the feasibility and effectiveness of antiviral treatment using pegylated interferon alpha-2a (pIFN α-2a) as an adjunct to induction and maintenance therapy in patients with ENKTCL. A total of seven patients with newly diagnosed EBV-positive ENKTCL were enrolled. Pegylated IFN α-2a was administered during induction chemoradiotherapy. If patients achieved a partial or complete response (PR or CR, respectively), high-dose chemotherapy with autologous stem cell transplantation (HDT/SCT) was given. After transplantation, maintenance therapy included pIFN α-2a for 3 years. Of the patients available for evaluation, all achieved a CR or PR after induction therapy but one patient relapsed before HDT/SCT. The event free survival and overall survival at 3 years were 50.0 ± 20.4% and 66.7 ± 19.2%, respectively. The 3-year disease-free survival after transplantation of the patients that received maintenance therapy was 80.0 ± 17.9%. The results of this pilot study indicated that pIFN α-2a containing induction and maintenance therapy was feasible and effective for ENKTCL.
机译:爱泼斯坦-巴尔病毒(EBV)在结外自然杀手/ T细胞淋巴瘤(ENKTCL)的发病机理中的作用及其对化学疗法的耐药性增加了抗病毒治疗策略的可能性。这项前瞻性研究的目的是评估使用聚乙二醇化干扰素α-2a(pIFNα-2a)作为ENKTCL患者诱导和维持治疗的辅助药物进行抗病毒治疗的可行性和有效性。共有7例新诊断为EBV阳性的ENKTCL患者入选。在诱导放化疗期间施用聚乙二醇化的IFNα-2a。如果患者获得部分或完全缓解(分别为PR或CR),则应进行大剂量化学疗法加自体干细胞移植(HDT / SCT)。移植后,维持治疗包括3年的pIFNα-2a。在可供评估的患者中,所有患者均在诱导治疗后达到了CR或PR,但一名患者在HDT / SCT之前复发。 3年无事件生存率和总生存率分别为50.0±20.4%和66.7±19.2%。接受维持治疗的患者移植后的3年无病生存率为80.0±17.9%。这项初步研究的结果表明,包含诱导和维持疗法的pIFNα-2a对于ENKTCL是可行和有效的。

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