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硼替佐米联合地塞米松治疗后行减低剂量异基因干细胞移植治疗自体移植高剂量化疗难治性多发性骨髓瘤

[Bortezomib plus dexamethasone treatment followed by reduced-intensity allogeneic stem cell transplantation for multiple myeloma refractory to high-dose chemotherapy with autologous transplantation].

作者信息

Hayashi Toshiaki, Yasui Hiroshi, Kawakami Kentaro, Ikeda Hiroshi, Takahashi Fumihiko, Kobayashi Toshihisa, Nishimura Susumu, Ishida Tadao, Imai Kohzoh, Shinomura Yasuhisa

机构信息

First Department of Internal Medicine, Sapporo Medical University School of Medicine.

出版信息

Rinsho Ketsueki. 2011 Mar;52(3):136-41.

Abstract

We present two long-term survivors after allogeneic transplantation with reduced-intensity conditioning regimen following relapse after autologous stem cell transplantation (ASCT) for multiple myeloma (MM). The first case was a 47-year-old male with IgG MM treated with 2 courses of high-dose melphalan along with ASCT and thalidomide, resulting in a minimal response. He then received 2 courses of bortezomib plus dexamethasone (BD) regimen, which was discontinued due to peripheral neuropathy. Allogeneic peripheral stem cell transplantation (PBSCT) from a sibling donor was performed after pretreatment with fludarabin (125 mg/m(2)) and melphalan (100 mg/m(2)). Engraftment was observed on day 11 and monoclonal IgG had disappeared 5 months after transplantation. The patient has been in complete remission for more than two and a half years with moderate chronic graft-versus-host disease (GVHD). The second case was a 51-year-old male who relapsed after ASCT for IgA MM. After 3 courses of BD treatment, irradiation to lumbar plasmacytoma, and thalidomide therapy, he received allogeneic PBSCT from a related donor after the same reduced intensity conditioning as performed in case 1. A complete response was observed 6 months after PBSCT. The patient has remained relapse-free for two years without GVHD. BD treatment followed by allogeneic stem cell transplantation with reduced intensity conditioning is supposed to be one of the most powerful strategies for patients showing relapse after ASCT.

摘要

我们报告了两例多发性骨髓瘤(MM)患者,他们在自体干细胞移植(ASCT)后复发,接受了减低强度预处理方案的异基因移植并长期存活。第一例是一名47岁的男性IgG MM患者,接受了2个疗程的大剂量美法仑联合ASCT及沙利度胺治疗,疗效甚微。随后他接受了2个疗程的硼替佐米联合地塞米松(BD)方案,但因周围神经病变而停药。在接受氟达拉滨(125 mg/m²)和马法兰(100 mg/m²)预处理后,进行了来自同胞供者的异基因外周干细胞移植(PBSCT)。第11天观察到植入,移植后5个月单克隆IgG消失。患者已完全缓解超过两年半,伴有中度慢性移植物抗宿主病(GVHD)。第二例是一名51岁的男性,他在ASCT治疗IgA MM后复发。在接受3个疗程的BD治疗、腰椎浆细胞瘤放疗及沙利度胺治疗后,他接受了与第一例相同的减低强度预处理的来自相关供者的异基因PBSCT。PBSCT后6个月观察到完全缓解。患者已无复发存活两年,无GVHD。对于ASCT后复发的患者,BD治疗后进行减低强度预处理的异基因干细胞移植被认为是最有效的策略之一。

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