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使用基因分型 HLA 相同和替代供体进行异基因骨髓移植治疗复发难治性淋巴瘤。

Allogeneic bone marrow transplantation for relapsed and refractory lymphoma using genotypically HLA-identical and alternative donors.

作者信息

Lundberg J H, Hansen R M, Chitambar C R, Lawton C A, Gottlieb M, Anderson T, Ash R C

机构信息

Department of Medicine, Medical College of Wisconsin, Milwaukee 53226.

出版信息

J Clin Oncol. 1991 Oct;9(10):1848-59. doi: 10.1200/JCO.1991.9.10.1848.

Abstract

Twenty-two patients, ages 16.6 to 43.9 years (median age, 30 years), with relapsed or refractory lymphoma were treated by allogeneic bone marrow transplantation after high-dose chemotherapy with or without total body irradiation (TBI). Seven patients had Hodgkin's disease, four had low-grade histology non-Hodgkin's lymphoma (NHL), seven had intermediate-grade NHL, and four had high-grade NHL. Of the 22 patients, 17 received T-cell (CD-3)-depleted marrow after intensive pretransplant chemoradiotherapy, and five received T-cell-replete grafts after chemotherapy-based preparative regimens. Five patients were transplanted from donors other than genotypically HLA-identical siblings: four from partially HLA-matched relatives, and one from a phenotypically HLA-identical unrelated donor. Acute graft-versus-host disease (GVHD) was less than or equal to grade II in all patients, and chronic GVHD was limited or absent in all but one patient. Of the 21 assessable patients, 17 (80.9%) achieved complete remissions. Death due to transplant-associated complications occurred in five patients, and five patients have relapsed. Thirteen patients are alive, and 12 are continuously relapse-free at a median follow-up of longer than 28 months (range, greater than 10 to greater than 58 months) from transplant. The cumulative probability of treatment failure from relapse or progression of lymphoma was 29% (95% confidence interval [CI], 12% to 51%), while the actuarial lymphoma-free (ie, event-free) survival plateau is 54.6% (95% CI, 34% to 76%). For young patients with advanced malignant lymphoma, allogeneic bone marrow transplantation appears superior to salvage chemotherapy for achievement of long-term, lymphoma-free survival and may be preferable to autologous bone marrow transplantation for selected patients.

摘要

22例年龄在16.6至43.9岁(中位年龄30岁)的复发或难治性淋巴瘤患者,在接受大剂量化疗联合或不联合全身照射(TBI)后接受了异基因骨髓移植。7例患有霍奇金病,4例为低级别组织学非霍奇金淋巴瘤(NHL),7例为中级别NHL,4例为高级别NHL。22例患者中,17例在强化移植前放化疗后接受了T细胞(CD-3)去除的骨髓,5例在基于化疗的预处理方案后接受了T细胞充足的移植物。5例患者的供体不是基因型HLA相同的同胞:4例来自部分HLA匹配的亲属,1例来自表型HLA相同的无关供体。所有患者的急性移植物抗宿主病(GVHD)均小于或等于II级;除1例患者外,所有患者的慢性GVHD均有限或不存在。在21例可评估的患者中,17例(80.9%)实现了完全缓解。5例患者死于移植相关并发症,5例患者复发。13例患者存活,12例在移植后中位随访时间超过28个月(范围,大于10至大于58个月)时持续无复发。淋巴瘤复发或进展导致治疗失败的累积概率为29%(95%置信区间[CI],12%至51%),而无淋巴瘤(即无事件)生存的精算平台期为54.6%(95%CI,34%至76%)。对于晚期恶性淋巴瘤的年轻患者,异基因骨髓移植在实现长期无淋巴瘤生存方面似乎优于挽救性化疗,对于部分患者可能优于自体骨髓移植。

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