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多发性骨髓瘤自体干细胞移植的大剂量治疗:过去、现在与未来

High-dose treatment with autologous stem cell transplantation in multiple myeloma: past, present, and future.

作者信息

Björkstrand Bo, Gahrton Gösta

机构信息

Department of Hematology, Karolinska Institute at Karolinska University Hospital Huddinge, Stockholm, Sweden.

出版信息

Semin Hematol. 2007 Oct;44(4):227-33. doi: 10.1053/j.seminhematol.2007.08.010.

Abstract

High-dose chemotherapy (HDT) with autologous stem cell transplantation (ASCT) has been used in the treatment of multiple myeloma since the early 1980s. Its present position as the backbone of first-line treatment in patients up to 60 to 65 years of age is the result of several controlled randomized trials, where its superiority over standard chemotherapy has been demonstrated. However, the method is not considered to have curative potential, with the possible exception of a small proportion of about 5% to 10% of patients with very long-standing complete remissions (CRs) of more than 8 years. Over the years, there have been several attempts to improve the technique, where, for example, tandem transplants and post-transplant maintenance treatment have been successful, at least in certain subgroups of patients, while others, such as graft purging, have been of no value. Treatment results need further improvement, particularly in poor-prognosis disease--based on abnormal karyotype and high beta2-microglobulin--and the future will show if the introduction of novel drugs like bortezomib, thalidomide, and lenalidomide will lead to longer survival and prolongation of disease control in multiple myeloma.

摘要

自20世纪80年代初以来,高剂量化疗(HDT)联合自体干细胞移植(ASCT)一直用于治疗多发性骨髓瘤。其目前作为60至65岁患者一线治疗支柱的地位,是多项对照随机试验的结果,这些试验证明了其优于标准化疗。然而,该方法不被认为具有治愈潜力,约5%至10%的患者可能是例外,这些患者能实现超过8年的长期完全缓解(CR)。多年来,人们多次尝试改进该技术,例如串联移植和移植后维持治疗已取得成功,至少在某些亚组患者中如此,而其他一些方法,如移植物净化,则没有价值。治疗结果需要进一步改善,特别是在基于异常核型和高β2微球蛋白的预后不良疾病中,未来将表明硼替佐米、沙利度胺和来那度胺等新药的引入是否会延长多发性骨髓瘤患者的生存期并延长疾病控制时间。

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