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首页> 外文期刊>Neurology: Official Journal of the American Academy of Neurology >Lenalidomide long-term neurotoxicity: Clinical and neurophysiologic prospective study
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Lenalidomide long-term neurotoxicity: Clinical and neurophysiologic prospective study

机译:Lenalidomide长期神经毒性:临床和神经生理前瞻性研究

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Objective:To evaluate long-term lenalidomide neurotoxicity and correlation with cumulative dose and hematologic response.Methods:Nineteen myeloma patients (7 men, mean age 63.2 years) underwent clinical and neurophysiologic assessment at baseline and at 2 (8 patients, group A) or 5 years (11 patients, group B) after starting lenalidomide therapy for relapsed/refractory multiple myeloma. Neuropathy was scored with Total Neuropathy Score clinical version (TNSc). Lenalidomide cumulative dose was correlated with severity of neuropathy and hematologic response.Results:At enrollment, 7/19 patients (3 in group A, 4 in group B) had neurophysiologic signs of neuropathy secondary to previous chemotherapy, in 2 of them subclinical. Neurophysiologic evidence of sensory axonal neuropathy occurred in 4/8 patients at 2 years follow-up (group A) and in 3/11 patients at 5 years follow-up (group B). Dorsal sural nerve sensory action potential amplitude was the earliest neurophysiologic abnormality. No relevant (4) clinical changes were found in TNSc score. Hematologic overall response was 62% in group A and 100% in group B. No correlation was found between lenalidomide cumulative dose and neuropathy or between neuropathy and hematologic response.Conclusions:In our study, up to 50% of myeloma patients on long-term lenalidomide therapy developed sensory axonal neuropathy. Reduced dorsal sural nerve sensory action potential amplitude was the first neurophysiologic alteration. Neuropathy was usually subclinical or mild, however. Neurotoxicity was independent of lenalidomide cumulative dose and hematologic response.
机译:目的:探讨长期lenalidomide神经毒性和累积相关剂量和血液反应。骨髓瘤患者(7人,平均年龄63.2岁)进行了临床和神经生理评估基线和2(8个病人,A组)或5年(11例,B组)lenalidomide开始治疗复发/难治性多发性骨髓瘤。与神经病变总分得分临床吗版本(TNSc)。与神经病变的严重程度有关血液反应。患者(B组3组,4)神经生理神经病变次要的迹象之前的化疗,其中2亚临床。感觉轴突的神经生理学证据神经病变发生在4/8患者2年后续在3/11患者(A组)和5年随访(B组)。背腓肠神经感觉动作电位振幅是最早的神经生理异常。(4)有关临床TNSc中发现了变化得分。A组100%,b组没有相关性发现lenalidomide累积剂量神经病变、神经病变和血液之间响应。对长期lenalidomide骨髓瘤患者治疗感觉轴突的神经病变。减少背腓肠神经感觉行动潜在的振幅是第一个神经生理改变。然而,通常是亚临床或轻微。神经毒性是lenalidomide的独立累积剂量和血液反应。

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