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使用噻替派、氟达拉滨和美法仑进行的减低强度预处理在晚期多发性骨髓瘤中是有效的。

Reduced intensity conditioning with thiotepa, fludarabine, and melphalan is effective in advanced multiple myeloma.

作者信息

Majolino Ignazio, Davoli Marina, Carnevalli Ellen, Locasciulli Anna, Di Bartolomeo Paolo, Scimè Rosanna, Corradini Paolo, Selleri Carmine, Narni Franco, Musso Maurizio, Bregni Marco, Olivieri Attilio, De Fabritiis Paolo, Pogliani Luigi, Arbelaez Jorge E Duque, Ruscio Carla, Bacigalupo Andrea

机构信息

Hematology and Bone Marrow Transplantation Unit, Azienda Ospedaliera S. Camillo-Forlanini, Rome, Italy.

出版信息

Leuk Lymphoma. 2007 Apr;48(4):759-66. doi: 10.1080/10428190601186150.

Abstract

Fifty-three patients with multiple myeloma (MM) underwent an allogeneic stem cell transplant (HSCT) from their HLA identical siblings using a reduced-intensity conditioning consisting of thioteopa 5 mg/kg, fludarabine 90 mg/m(2), and melphalan 80 mg/m(2). Their median age was 52 years (range 38 - 68) and the interval from diagnosis 12 months. Forty-three patients (82%) had advanced disease and 33 had previously been treated with high-dose therapy with one (N = 21), or more (N = 12) autologus transplants. Ten (18%) had their allograft programmed after induction chemotherapy. The majority (N = 44) received peripheral blood as stem cell source. Acute graft-versus-host disease (GVHD) grade II - IV developed in 45%, but grade III - IV in only 5%. Cumulative incidence of chronic GVHD was 64%. Sixty-two per cent were in complete remission (CR) following transplantation. Transplant-related mortality was 13%. Relapse incidence was 32%. With a median follow-up of 22 months, 3-year overall survival is 45% and progression free survival (PFS) 37%. The thiotepa, fludarabine, and melphalan conditioning regimen can produce remissions in the majority of MM patients with a limited transplant mortality rate. When used as first line treatment the results of transplantation appear even more encouraging.

摘要

53例多发性骨髓瘤(MM)患者接受了来自 HLA 配型相同同胞的异基因干细胞移植(HSCT),预处理采用低强度方案,包括硫替派5mg/kg、氟达拉滨90mg/m²和马法兰80mg/m²。患者的中位年龄为52岁(范围38 - 68岁),从诊断到移植的间隔时间为12个月。43例(82%)患者病情处于进展期,33例患者此前接受过高剂量治疗,其中21例接受过1次自体移植,12例接受过1次以上自体移植。10例(18%)患者在诱导化疗后进行了异基因移植计划。大多数患者(44例)接受外周血作为干细胞来源。急性移植物抗宿主病(GVHD)Ⅱ - Ⅳ级的发生率为45%,但Ⅲ - Ⅳ级仅为5%。慢性GVHD的累积发生率为64%。移植后62%的患者达到完全缓解(CR)。移植相关死亡率为13%。复发率为32%。中位随访22个月时,3年总生存率为45%,无进展生存率(PFS)为37%。硫替派、氟达拉滨和马法兰预处理方案可使大多数MM患者获得缓解,且移植死亡率有限。当作为一线治疗时,移植结果似乎更令人鼓舞。

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