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Allogeneic bone marrow transplantation for low-grade lymphoma and chronic lymphocytic leukemia.

机译:同种异体骨髓移植用于低度淋巴瘤和慢性淋巴细胞性白血病。

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Twenty-six patients with low-grade lymphoma (LGL) (n = 18) or chronic lymphocytic leukemia (CLL) (n = 8) received allogeneic BMTs between 1985 and 1998. Median age was 42 years, median interval from diagnosis to transplant 22 months and median number of prior treatments three. Twenty (77%) had stage IV disease; 22 (85%) had never achieved CR. Donor source was HLA matched sibling (n = 19, 73%), matched unrelated (n = 6, 23%) or syngeneic (n = 1). Conditioning therapy included total body irradiation in 23 patients and busulphan in three. Twenty-five received GVHD prophylaxis with cyclosporine A; + methotrexate (n = 19), + methylprednisolone (n = 2) or + T cell depletion of allograft +/- methotrexate (n = 4). Sixteen patients are alive, a median of 2.4 years post BMT. Death occurred due to transplant complications (n = 7) or underlying disease (n = 3). Eighteen (12 LGL, six CLL) of 22 evaluable patients (82%) achieved CR post BMT. Cumulative incidence of refractory/recurrent disease was 18% (95% confidence interval (CI) 7-42%). Overall and event-free survivals were 58% (95% CI 35-75%) and 54% (95% CI 32-72%), respectively. Allogeneic BMT for young patients with advanced LGL or CLL is feasible and can result in long-term disease-free survival.
机译:1985年至1998年间,有26例低度淋巴瘤(LGL)(n = 18)或慢性淋巴细胞性白血病(CLL)(n = 8)患者接受了同种异体BMT。中位年龄为42岁,从诊断到移植的平均间隔22个月和先前治疗的中位数三。二十名(77%)患有IV期疾病; 22(85%)从未达到CR。供体来源是HLA匹配的同胞(n = 19,73%),匹配的无关(n = 6、23%)或同系(n = 1)。调理疗法包括23例患者进行全身放射治疗,三例采用Busulphan治疗。 25名接受环孢霉素A预防GVHD的患者; +甲氨蝶呤(n = 19),+甲基泼尼松龙(n = 2)或+同种异体移植物+/-甲氨蝶呤(n = 4)的T细胞耗竭。 16名患者还活着,中位数为BMT后2.4年。因移植并发症(n = 7)或潜在疾病(n = 3)导致死亡。 22名可评估患者中的18名(12 LGL,6 CLL)(82%)在BMT后获得CR。顽固性/复发性疾病的累积发生率为18%(95%置信区间(CI)7-42%)。总体生存率和无事件生存率分别为58%(95%CI 35-75%)和54%(95%CI 32-72%)。对于患有晚期LGL或CLL的年轻患者,同种异体BMT是可行的,并可导致长期无病生存。

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