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首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Hematological and cytogenetic response of interferon alpha 2b alone and combined interferon alpha plus cytarabine as a first-line treatment in chronic myeloid leukemia.
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Hematological and cytogenetic response of interferon alpha 2b alone and combined interferon alpha plus cytarabine as a first-line treatment in chronic myeloid leukemia.

机译:干扰素α2b单独和联合干扰素α加阿糖胞苷作为慢性髓样白血病的一线治疗的血液学和细胞遗传学反应。

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摘要

Treatment with interferon-alpha (IFNalpha) prolongs survival in chronic myeloid leukemia (CML). Additionally, cytarabine (AraC) can reduce the number of Ph + metaphases. Fortythree previously untreated patients with CML in chronic phase were randomly assigned to receive either. IFNalpha 2b (5 MU sqm/daily) or IFNalpha 2b in the same dosages plus monthly courses of low-dose AraC. The aim were complete hematologic remission at 6 months and cytogenetic response at 12 months. A complete hematologic remission occurred in 60.4% patients with single IFNalpha 2b in 76.2% patients with combination therapy. A cytogenetic response was present in 13.9% (major in 2 patients) with IFN therapy and in 38.1% patients with combination therapy. Two of 21 patients treated with IFNalpha/AraC therapy achieved major (9.52%), 4 partial (19.04%) and 2 minor (9.52%) cytogenetic response. Major side effects were cytopenia (20.1%), flu-like syndromes (42.4%) and increase of hepatic transaminases (3.4%). The side effects were more significant in the group receiving combination therapy. Based on published data that show a survival advantage for patients who achieved any cytogenetic response, and high rate of cytogenetic response which we observed in our study we believe that IFN plus AraC regimen could be a front-line therapy for CML.
机译:干扰素-α(IFNalpha)的治疗可延长慢性粒细胞白血病(CML)的生存期。另外,阿糖胞苷(AraC)可以减少Ph +中期的数量。先前未接受治疗的慢性期CML患者43例被随机分配接受其中任一者。相同剂量的IFNalpha 2b(每天5 MU sqm)或IFNalpha 2b加上低剂量AraC的每月疗程。目的是在6个月时完全血液学缓解,在12个月时发生细胞遗传学反应。联合治疗的76.2%的患者中,有60.4%的单一IFNalpha 2b患者发生了完全的血液学缓解。接受IFN治疗的患者发生细胞遗传学应答的比例为13.9%(2位患者中为严重),接受联合治疗的患者中存在38.1%的患者。在接受IFNalpha / AraC治疗的21例患者中,有2例达到了主要(9.52%),4例(19.04%)和2例(9.52%)的细胞遗传学应答。主要副作用是血细胞减少症(20.1%),流感样综合征(42.4%)和肝转氨酶升高(3.4%)。在接受联合治疗的组中,副作用更为明显。根据已发表的数据,这些数据显示了对任何细胞遗传学应答和高细胞遗传学应答率患者的生存优势,我们在研究中观察到这一点,我们认为IFN加AraC方案可能是CML的一线治疗方法。

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