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Peripheral blood lymphocyte telomere length as a predictor of response to immunosuppressive therapy in childhood aplastic anemia

机译:外周血淋巴细胞端粒长度可预测儿童再生障碍性贫血对免疫抑制疗法的反应

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摘要

Predicting the response to immunosuppressive therapy could provide useful information to help the clinician define treatment strategies for patients with aplastic anemia. In our current study, we evaluated the relationship between telomere length of lymphocytes at diagnosis and the response to immunosuppressive therapy in 64 children with aplastic anemia, using flow fluorescence in situ hybridization. Median age of patients was ten years (range 1.5–16.2 years). Severity of the disease was classified as very severe in 23, severe in 21, and moderate in 20 patients. All patients were enrolled in multicenter studies using antithymocyte globulin and cyclosporine. The response rate to immunosuppressive therapy at six months was 52% (33 of 64). The probability of 5-year failure-free survival and overall survival were 56% (95% confidence interval (CI): 41–69%) and 97% (95%CI: 87–99%), respectively. Median telomere length in responders was −0.4 standard deviation (SD) (−2.7 to +3.0 SD) and −1.5 SD (−4.0 to +1.6 (SD)) in non-responders (P<0.001). Multivariate analysis showed that telomere length shorter than −1.0 SD (hazard ratio (HR): 22.0; 95%CI: 4.19–115; P<0.001), platelet count at diagnosis less than 25×109/L (HR: 13.9; 95%CI: 2.00–96.1; P=0.008), and interval from diagnosis to immunosuppressive therapy longer than 25 days (HR: 4.81; 95%CI: 1.15–20.1; P=0.031) were the significant variables for poor response to immunosuppressive therapy. Conversely to what has been found in adult patients, measurement of the telomere length of lymphocytes at diagnosis is a promising assay in predicting the response to immunosuppressive therapy in children with aplastic anemia.
机译:预测对免疫抑制疗法的反应可能会提供有用的信息,以帮助临床医生确定再生障碍性贫血患者的治疗策略。在我们目前的研究中,我们使用流式荧光原位杂交技术评估了64例再生障碍性贫血患儿诊断时淋巴细胞端粒长度与免疫抑制治疗反应之间的关系。患者的中位年龄为十年(1.5-16.2岁)。该疾病的严重程度被分类为非常严重的23例,严重的21例和中度的20例。所有患者均接受了使用抗胸腺细胞球蛋白和环孢霉素的多中心研究。六个月对免疫抑制疗法的反应率为52%(64中的33)。 5年无故障生存率和总生存率分别为56%(95%置信区间(CI):41–69%)和97%(95%CI:87–99%)。应答者中端粒的中位长度为-0.4标准偏差(SD)(-2.7至+3.0 SD)和非应答者中-1.5 SD(-4.0至+1.6(SD))(P <0.001)。多因素分析显示端粒长度短于−1.0 SD(危险比(HR):22.0; 95%CI:4.19–115; P <0.001),诊断时血小板计数低于25×10 9 / L(HR:13.9; 95%CI:2.00–96.1; P = 0.008),以及从诊断到免疫抑制治疗的间隔时间超过25天(HR:4.81; 95%CI:1.15-20.1; P = 0.031)对免疫抑制治疗反应差的重要变量。与成年患者相反,诊断时测量淋巴细胞端粒长度是预测再生障碍性贫血儿童对免疫抑制疗法反应的一种有前途的测定方法。

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