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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Lack of neuroprotection by an ACTH (4-9) analogue. A randomized trial in patients treated with vincristine for Hodgkin's or non-Hodgkin's lymphoma.
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Lack of neuroprotection by an ACTH (4-9) analogue. A randomized trial in patients treated with vincristine for Hodgkin's or non-Hodgkin's lymphoma.

机译:ACTH(4-9)类似物缺乏神经保护作用。长春新碱治疗霍奇金淋巴瘤或非霍奇金淋巴瘤的一项随机试验。

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PURPOSE: This randomized, double-blind, placebo-controlled study evaluates the effect of the corticotropin (4-9) analogue Org 2766 on the neuropathy-free interval in patients receiving vincristine (VCR) containing chemotherapy for Hodgkin's or non-Hodgkin's lymphoma. PATIENTS AND METHODS: In a longitudinal design, 150 patients were evaluated by interview, neurological examination, and neurophysiological techniques. Patients with an expected cumulative VCR dose of at least 8 mg received a single dose of Org 2766 or placebo before and after each intravenous VCR injection and 3-4 weeks after cessation of VCR. The final patient assessment was performed 1 month after discontinuation of study medication. The neuropathy-free interval as the major end point of this study was defined as the first occurrence of bilateral paresthesias and expressed as the administered cumulative VCR dose. This bi-center study represents the largest cohort of patients monitored for the effect of an ACTH-analogue on VCR neurotoxicity. RESULTS: A total of 147 patients were included in the final analysis. No significant differences were observed between the placebo and actively treated group for the major and secondary endpoints. CONCLUSION: Contrary to a single previous pilot study in patients receiving VCR-based chemotherapy, in our study the ACTH (4-9) analogue Org 2766 did not provide protection from VCR-induced neuropathy.
机译:目的:这项随机,双盲,安慰剂对照的研究评估了促肾上腺皮质激素(4-9)类似物Org 2766对接受长春新碱(VCR)含霍奇金或非霍奇金淋巴瘤化疗的患者的无神经病间隔的影响。患者和方法:在纵向设计中,通过访谈,神经系统检查和神经生理学技术对150例患者进行了评估。预期VCR累积累积量至少为8 mg的患者在每次静脉内VCR注射之前和之后以及停止VCR后3-4周接受一剂Org 2766或安慰剂。在终止研究药物治疗后1个月进行了最终患者评估。无神经病间隔作为该研究的主要终点,被定义为双侧感觉异常的首次发生,并表示为累积的VCR剂量。这项双中心研究代表了接受ACTH类似物对VCR神经毒性作用监测的最大患者队列。结果:最终分析共纳入147例患者。在主要和次要终点,安慰剂组和积极治疗组之间未观察到显着差异。结论:与先前的一项基于VCR的化疗患者的前期研究相反,在我们的研究中,ACTH(4-9)类似物Org 2766没有提供针对VCR诱发的神经病的保护作用。

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