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异基因外周血干细胞移植治疗高危非霍奇金淋巴瘤。

Allogeneic peripheral blood stem cell transplantation for high-risk non-Hodgkin's lymphoma.

作者信息

Seropian S, Bahceci E, Cooper D L

机构信息

Section of Medical Oncology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

出版信息

Bone Marrow Transplant. 2003 Oct;32(8):763-9. doi: 10.1038/sj.bmt.1704233.

Abstract

A high incidence of nonrelapse mortality (NRM) has limited the use of allogeneic transplantation for poor prognosis non-Hodgkin's lymphoma (NHL). We sought to improve the outcome of allografting by utilizing Filgrastim-mobilized peripheral blood stem cells (PBSC) in combination with either standard ablative or reduced-intensity conditioning. A total of 21 patients with intermediate/high-grade lymphoma and seven patients with low-grade histology were enrolled on protocols using PBSC. All patients were considered high risk for recurrence and/or NRM because of age >50 (n=16), refractory disease (n=17), failed autologous transplant (n=11) and abnormal organ function (n=2). In all, 17 patients received ablative regimens and 11 received modified conditioning including fludarabine, intravenous busulfan and ATG. Tacrolimus and mini-dose methotrexate were used for graft-versus-host-disease (GVHD) prophylaxis. Median follow-up was 38 months. Disease-free and overall survival were 57 and 58%. Seven of the 11 patients who relapsed after a previous transplant remain disease free. Four of the 10 patients with recurrent/persistent disease post transplant responded to additional therapy including withdrawal of immunosuppression+/-DLI. These results support a potent graft-versus-lymphoma effect and suggest that patients who relapse after an autologous transplant can be salvaged with an allogeneic transplant.

摘要

非复发死亡率(NRM)较高限制了异基因移植在预后不良的非霍奇金淋巴瘤(NHL)中的应用。我们试图通过使用非格司亭动员的外周血干细胞(PBSC)联合标准清髓或减低强度预处理来改善移植结局。共有21例中/高度淋巴瘤患者和7例低级别组织学患者入组使用PBSC的方案。所有患者因年龄>50岁(n = 16)、难治性疾病(n = 17)、自体移植失败(n = 11)和器官功能异常(n = 2)而被认为有复发和/或NRM的高风险。总共17例患者接受了清髓方案,11例接受了改良预处理,包括氟达拉滨、静脉注射白消安和抗胸腺细胞球蛋白。他克莫司和小剂量甲氨蝶呤用于预防移植物抗宿主病(GVHD)。中位随访时间为38个月。无病生存率和总生存率分别为57%和58%。11例先前移植后复发的患者中有7例仍无病生存。10例移植后复发/持续疾病的患者中有4例对包括停用免疫抑制+/-供者淋巴细胞输注(DLI)在内的额外治疗有反应。这些结果支持了强大的移植物抗淋巴瘤效应,并表明自体移植后复发的患者可以通过异基因移植挽救。

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