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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Immunosuppressive therapy for myelodysplastic syndrome: efficacy of methylprednisolone pulse therapy with or without cyclosporin A.
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Immunosuppressive therapy for myelodysplastic syndrome: efficacy of methylprednisolone pulse therapy with or without cyclosporin A.

机译:骨髓增生异常综合症的免疫抑制疗法:有或没有环孢菌素A的甲基强的松龙脉冲疗法的疗效。

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摘要

We investigated whether immunosuppressive therapy using methylprednisolone (mPSL) with or without cyclosporin A (CsA) could benefit patients with myelodysplastic syndrome (MDS). Eligibility criteria for this study were a clinical diagnosis of MDS with less than 5% blast in peripheral blood, less than 10% blast in bone marrow and advanced cytopenia. Among 73 patients with MDS, 18 eligible and consecutive patients (8 men and 10 women), aged 48 to 87 years (median: 66.5 years) were assigned to receive mPSL pulse therapy (1,000 mg daily for 3 consecutive days, followed by tapering oral prednisolone; n= 12) or mPSL pulse with CsA therapy (4 to 5 mg/kg administered twice daily; n= 6). Six of 18 patients (33.3%; 3 of 10 patients with RA, 2 of 6 patients with RAEB, 1 of 2 patients with CMMoL) responded to immunosuppressive therapy. Four patients responded to mPSL pulse alone, and two patients responded to mPSL pulse with CsA. One of 6 patients with hypocellular bone marrow and 5 of 12 patients with normocellular or hypercellular marrow responded to immunosuppressive therapy. No patient with myelofibrosis responded to the therapy. The duration of response ranged from 4 to 59 months (median: 14 months). Although a significant difference was observed between responders and nonresponders in the survival rate ( P<0.05), no significant difference was found in clinical characteristics at entry between responders and nonresponders. In responders, mean hemoglobin levels were significantly increased ( P<0.01), and the required red cell transfusion dose was significantly reduced ( P<0.01). It is possible that immunosuppressive therapy might be effective for a certain subset of patients with MDS.
机译:我们调查了使用甲基强的松龙(mPSL)或不使用环孢菌素A(CsA)的免疫抑制疗法是否可以使患有骨髓增生异常综合症(MDS)的患者受益。这项研究的资格标准是MDS的临床诊断,其外周血中原始细胞少于5%,骨髓中原始细胞少于10%,晚期血细胞减少症。在73名MDS患者中,年龄在48至87岁(中位数:66.5岁)的18例合格且连续的患者(8例男性和10例女性)被分配接受mPSL脉冲疗法(连续3天每天1,000 mg,然后逐渐减少口服剂量)泼尼松龙; n = 12)或mPSL脉搏用CsA治疗(每天2次,每次4至5 mg / kg; n = 6)。 18例患者中有6例(33.3%; 10例RA患者中有3例,RAEB 6例患者中有2例,CMMoL 2例患者中有1例)对免疫抑制疗法产生了反应。四名患者仅对mPSL脉冲有反应,而两名患者对CsA对mPSL脉冲有反应。 6例低细胞性骨髓的患者中有1例和12例正常细胞或高细胞性骨髓的患者中的5例对免疫抑制疗法有反应。没有骨髓纤维化的患者对该疗法有反应。反应持续时间为4到59个月(中位数:14个月)。尽管观察到反应者和非反应者的生存率有显着差异(P <0.05),但反应者和非反应者进入时的临床特征没有发现显着差异。在应答者中,平均血红蛋白水平显着增加(P <0.01),所需的红细胞输注剂量显着降低(P <0.01)。免疫抑制疗法可能对某些MDS患者有效。

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