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一种新型的降低强度预处理方案用于异基因造血干细胞移植,与移植物抗宿主病发生率降低相关。

A novel reduced intensity regimen for allogeneic hematopoietic stem cell transplantation associated with a reduced incidence of graft-versus-host disease.

作者信息

Miller K B, Roberts T F, Chan G, Schenkein D P, Lawrence D, Sprague K, Gorgun G, Relias V, Grodman H, Mahajan A, Foss F M

机构信息

Department of Medicine, Bone Marrow Transplantation and Hematological Malignancy Unit, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

出版信息

Bone Marrow Transplant. 2004 May;33(9):881-9. doi: 10.1038/sj.bmt.1704454.

Abstract

In all, 55 patients at high risk or ineligible for a conventional allogeneic hematopoietic stem cell transplant (HSCT) received a regimen consisting of extracorporeal photopheresis, pentostatin, and reduced dose total body irradiation. The median age was 49 years (18-70 years); 44 received a sibling and 11 an unrelated HSCT; 44% were over the age of 50 years and 31% had undergone a prior HSCT. Graft-versus-host disease (GVHD) prophylaxis consisted of cyclosporine and methotrexate. Full donor chimerism was documented in 98% by day +100. The 1000-day nonrelapse mortality was 11%. The median follow-up is 502 days (154-1104 days). The 1- and 2-year overall survival (OS) and event-free survival (EFS) are 67, 58 and 55%, and 47%, respectively. Patients who had not received a prior HSCT or had less than three prior chemotherapy regimens had a 71% OS and 67% EFS at 1 year. Greater than grade II aGVHD developed in 9% and chronic GVHD (cGVHD) in 43%, and extensive in 12% and limited in 31%. Of the patients, 86% who engrafted had a disease response, 72% had complete and 14% partial responses. This novel reduced intensity preparative regimen was well tolerated and associated with a low incidence of transplant-related mortality and serious acute and cGVHD.

摘要

共有55例高风险或不符合传统异基因造血干细胞移植(HSCT)条件的患者接受了包括体外光化学疗法、喷司他丁和降低剂量全身照射的方案。中位年龄为49岁(18 - 70岁);44例接受同胞供者HSCT,11例接受非血缘HSCT;44%的患者年龄超过50岁,31%的患者曾接受过HSCT。移植物抗宿主病(GVHD)预防采用环孢素和甲氨蝶呤。到+100天时,98%的患者记录为完全供者嵌合。1000天非复发死亡率为11%。中位随访时间为502天(154 - 1104天)。1年和2年的总生存率(OS)和无事件生存率(EFS)分别为67%、58%和55%、47%。未接受过HSCT或既往化疗方案少于三个的患者1年OS为71%,EFS为67%。9%的患者发生大于II级急性GVHD,43%发生慢性GVHD(cGVHD),其中广泛型占12%,局限型占31%。在植入的患者中,86%有疾病反应,72%完全缓解,14%部分缓解。这种新型的低强度预处理方案耐受性良好,与移植相关死亡率以及严重急性和慢性GVHD的低发生率相关。

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