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首页> 外文期刊>Experimental and therapeutic medicine >Peripheral neuropathy outcomes and efficacy of subcutaneous bortezomib when combined with thalidomide and dexamethasone in the treatment of multiple myeloma
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Peripheral neuropathy outcomes and efficacy of subcutaneous bortezomib when combined with thalidomide and dexamethasone in the treatment of multiple myeloma

机译:硼替佐米联合沙利度胺和地塞米松治疗多发性骨髓瘤的周围神经病变结果和疗效

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Due to the safety, convenience and efficacy of subcutaneous administration of bortezomib (scBor), it is becoming increasingly common to treat multiple myeloma (MM) using this treatment method. The current retrospective study suggested a lower incidence of peripheral neuropathy (PN) outcomes and superior efficacy following treatment with scBor combined with thalidomide and dexamethasone (VTD) in MM when compared with intravenous Bor (ivBor) treatment. The data of 81 patients from the Affiliated Hospital of Nantong University between September 2011 and February 2014 were analyzed, including 37 scBor and 44 ivBor patients administered a median (range) of 5.5 (3-8) and 6 (3-10) chemotherapy cycles, respectively. Adverse events (AEs) were assessed according to the National Cancer Institute (NCI) Common Terminology Criteria for AEs, and response and progression were assessed by the International Myeloma Working Group criteria. Evidence of histopathology using transmission electron microscopy (TEM) was obtained from an in vivo model of adult Sprague Dawley (SD) rats. Following bortezomib-based VTD chemotherapy, patients had achieved very good partial remission or demonstrated no significant difference between the scBor and ivBor treatment groups (75.6 vs. 84.1%, respectively; P=0.350). The 1-year progression-free survival (83.8 vs. 84.1%, scBor vs. ivBor; P=0.921) and 1-year overall survival (OS) (91.9 vs. 90.9%, respectively; P=0.926) were also similar. PN rates of all the NCI grades were 51.3 and 61.3% (P=0.371); grade >= 2, 35.1 and 56.8% (P=0.052); and grade >= 3, 32.7 and 20.5% (P=0.015) in the subcutaneous and intravenous treatment groups, respectively, which suggests that severe PN may be less common following scBor treatment. There were no severe injection site reactions in the scBor-treated group. The incidence of adverse events were comparable between the two groups, including thrombocytopenia, anemia, fatigue and gastrointestinal symptoms such as nausea and vomiting. Furthermore, TEM images of the SD rat sciatic nerves revealed that all rats suffered PN to varying degrees, except the control group, and that the PN of ivBor-treated rats (in the presence and the absence of thalidomide) was more severe than that of scBor-treated rats. It was concluded that a subcutaneous dose of bortezomib of 1.3 mg/m(2) may result in a lower incidence and severity of PN, with equivalent efficacy, as a component of combination VTD chemotherapy.
机译:由于硼替佐米(scBor)皮下给药的安全性,便利性和有效性,使用这种治疗方法治疗多发性骨髓瘤(MM)变得越来越普遍。当前的回顾性研究表明,与静脉内Bor(ivBor)治疗相比,scBor联合沙利度胺和地塞米松(VTD)治疗MM后,周围神经病变(PN)的发生率较低,且疗效更高。分析了2011年9月至2014年2月南通大学附属医院的81例患者的数据,包括37位scBor和44位ivBor患者接受了5.5(3-8)和6(3-10)个化疗周期的中位数(范围) , 分别。根据美国国家癌症研究所(NCI)的AE通用术语标准评估不良事件(AE),并根据国际骨髓瘤工作组标准评估不良反应和进展。使用透射电子显微镜(TEM)的组织病理学证据是从成年Sprague Dawley(SD)大鼠的体内模型获得的。在以硼替佐米为基础的VTD化疗后,患者实现了很好的部分缓解,或在scBor和ivBor治疗组之间无显着差异(分别为75.6和84.1%; P = 0.350)。 1年无进展生存期(83.8 vs. 84.1%,scBor vs. ivBor; P = 0.921)和1年总生存期(OS)(分别为91.9 vs. 90.9%; P = 0.926)。所有NCI等级的PN率分别为51.3%和61.3%(P = 0.371); > = 2、35.1和56.8%(P = 0.052);皮下和静脉内治疗组分别≥3、32.7和20.5%(P = 0.015),这表明scBor治疗后严重的PN可能不那么常见。 scBor治疗组没有严重的注射部位反应。两组的不良事件发生率相当,包括血小板减少症,贫血,疲劳和胃肠道症状,如恶心和呕吐。此外,SD大鼠坐骨神经的TEM图像显示,除对照组外,所有大鼠均遭受不同程度的PN,并且ivBor处理的大鼠(在有和无沙利度胺的情况下)的PN均比对照组严重。经scBor处理的大鼠。结论是,硼替佐米皮下剂量为1.3 mg / m(2)可以降低PN的发生率和严重性,并且具有与VTD联合化疗相当的功效。

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