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[多发性骨髓瘤的新治疗策略以求治愈]

[New treatment strategy of multiple myeloma for cure].

作者信息

Murakami Hirokazu, Handa Hiroshi

机构信息

School of Health Sciences, Faculty of Medicine, Gunma University.

出版信息

Gan To Kagaku Ryoho. 2006 Apr;33(4):417-23.

Abstract

Multiple myeloma has long been considered an incurable disease. Indeed, the median survival time in patients treated with conventional chemotherapy has been reported to be about 3 years, and the survival rate decreased consecutively and was about 2 to 3% at 10 years. However, after introduction of autologous stem-cell transplantation in the 1990s, the median survival time was improved to about 5 years. Furthermore, novel drugs have been introduced in the treatment of patients with relapsed/refractory multiple myeloma, and improved the prognosis of these patients. Thalidomide, which has anti-angiogenetic activity, has a 30-40% response rate, and the combination of thalidomide and dexamethasone has a 40-50% response rate. Lenalidomide, which is a thalidomide analog, has a higher efficacy and lower incidence of adverse effects than thalidomide. Bortezomib, which is a proteasome inhibitor and inhibits NF-kappaB activity, has also excellent efficacy like thalidomide. The clinical trials using these drugs for newly diagnosed patients are now ongoing around the world, and show very excellent results. The good combination of stem-cell transplantation and novel drugs may well improve the prognosis of patients with multiple myeloma, and induce a cure,especially in young patients.

摘要

多发性骨髓瘤长期以来一直被认为是一种无法治愈的疾病。事实上,据报道,接受传统化疗的患者中位生存时间约为3年,生存率持续下降,10年时约为2%至3%。然而,在20世纪90年代引入自体干细胞移植后,中位生存时间提高到了约5年。此外,新型药物已被用于复发/难治性多发性骨髓瘤患者的治疗,并改善了这些患者的预后。具有抗血管生成活性的沙利度胺的缓解率为30%至40%,沙利度胺与地塞米松联合使用的缓解率为40%至50%。来那度胺是沙利度胺的类似物,其疗效高于沙利度胺,不良反应发生率更低。硼替佐米是一种蛋白酶体抑制剂,可抑制核因子κB活性,其疗效也与沙利度胺一样出色。目前全球正在进行使用这些药物治疗新诊断患者的临床试验,且结果非常出色。干细胞移植与新型药物的良好结合很可能会改善多发性骨髓瘤患者的预后,并实现治愈,尤其是在年轻患者中。

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