Mandigers C M, Raemaekers J M, Schattenberg A V, Roovers E A, Bogman M J, van der Maazen R W, De Pauw B E, De Witte T
Department of Medicine, University Hospital Nijmegen, The Netherlands.
Br J Haematol. 1998 Jan;100(1):198-206. doi: 10.1046/j.1365-2141.1998.00539.x.
We present the clinical results of allogeneic bone marrow transplantation (BMT) with T-cell-depleted grafts from HLA-matched sibling donors in patients with poor-risk relapsed low-grade non-Hodgkin's lymphoma (NHL). Poor risk was defined as relapse within 12 months after or progression during prior treatment. The conditioning regimen consisted of cyclophosphamide and total-body irradiation with or without additional idarubicin. Donor marrow was depleted of T lymphocytes using counterflow centrifugation. Post-BMT prophylaxis of graft-versus-host disease (GvHD) consisted of cyclosporine A. 15 patients with a median age of 47 years (range 30-57) were transplanted. All patients engrafted. After a median follow-up of 36 months (range 9-78), 10 patients were alive and in complete remission (CR). Two of them had relapsed after BMT but re-entered CR following infusions of leucocytes from the original bone marrow donor. Five patients died; causes of death were cardiomyopathy (n = 1), chronic GvHD (n = 1) and infection during chronic GvHD (n = 3). We conclude that allogeneic T-cell-depleted bone marrow transplantation is an efficacious treatment for patients with poor-risk relapsed low-grade NHL. Infusions of donor leucocytes reinduced CR in the two patients with relapse after BMT.
我们报告了采用来自 HLA 匹配同胞供者的 T 细胞去除移植物进行异基因骨髓移植(BMT)治疗预后不良的复发性低度非霍奇金淋巴瘤(NHL)患者的临床结果。预后不良定义为在先前治疗后 12 个月内复发或在先前治疗期间病情进展。预处理方案包括环磷酰胺和全身照射,可加用或不加用伊达比星。使用逆流离心法去除供体骨髓中的 T 淋巴细胞。BMT 后移植物抗宿主病(GvHD)的预防采用环孢素 A。15 例患者接受了移植,中位年龄为 47 岁(范围 30 - 57 岁)。所有患者均实现造血重建。中位随访 36 个月(范围 9 - 78 个月)后,10 例患者存活且处于完全缓解(CR)状态。其中 2 例在 BMT 后复发,但在输注来自原骨髓供体的白细胞后再次进入 CR 状态。5 例患者死亡;死亡原因分别为心肌病(n = 1)、慢性 GvHD(n = 1)以及慢性 GvHD 期间的感染(n = 3)。我们得出结论,异基因 T 细胞去除骨髓移植是治疗预后不良的复发性低度 NHL 患者的有效方法。输注供体白细胞使 2 例 BMT 后复发的患者再次诱导进入 CR 状态。