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脐血移植后供体来源的第二血液系统恶性肿瘤。

Donor-derived second hematologic malignancies after cord blood transplantation.

机构信息

Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Jul;16(7):1025-31. doi: 10.1016/j.bbmt.2010.02.014. Epub 2010 Feb 21.

Abstract

Double umbilical cord blood transplantation (UCBT) with a reduced-intensity conditioning regimen is an effective strategy for adult patients without a matched donor. The risk of second malignancies in these patients has not yet been established, however. In the present study, 98 adults with a hematologic malignancy underwent double UCBT. Seventy patients received a reduced-intensity conditioning regimen of fludarabine 30 mg/m(2)/day for 6 days, melphalan 100 mg/m(2)/day for 1 day, and rabbit antithymocyte globulin 1.5 mg/kg/day for 4 days, and 28 patients received a myeloablative total body radiation-containing conditioning regimen. Sixty-three patients received sirolimus-based graft-versus-host disease (GVHD) prophylaxis, and 35 patients received non-sirolimus-based GVHD prophylaxis. The median patient age was 48 years (range, 19-67 years). Eighteen patients developed a second malignancy at a median of 134 days after transplantation. Sixteen patients had lymphoma, and 2 patients had myelodysplasic syndrome/myeloproliferative disorder (MDS/MPD). Sixteen of these second malignancies (both cases of MDS/MPD and 14 of the lymphomas) were donor-derived; the origins of the others were not determined. GVHD prophylaxis, HLA matching, primary disease, age, total nucleated cell dose, and CD34(+) cell dose were not associated with a higher rate of second malignancy. Second myelogenous malignancies of donor origin occur after double UCBT, suggesting that a search for donor origin should be performed in all patients with suspected relapse.

摘要

双脐血干细胞移植(UCBT)联合强度降低的预处理方案是无匹配供体的成人患者的有效治疗策略。然而,这些患者的二次恶性肿瘤风险尚未确定。在本研究中,98 例血液系统恶性肿瘤患者接受了双 UCBT。70 例患者接受了强度降低的预处理方案,包括氟达拉滨 30mg/m²/天,共 6 天;马法兰 100mg/m²/天,共 1 天;兔抗胸腺细胞球蛋白 1.5mg/kg/天,共 4 天;28 例患者接受了含全身照射的清髓性预处理方案。63 例患者接受了西罗莫司为基础的移植物抗宿主病(GVHD)预防,35 例患者接受了非西罗莫司为基础的 GVHD 预防。中位患者年龄为 48 岁(范围,19-67 岁)。18 例患者在移植后中位 134 天发生二次恶性肿瘤。16 例患者患有淋巴瘤,2 例患者患有骨髓增生异常综合征/骨髓增殖性疾病(MDS/MPD)。这 18 例二次恶性肿瘤中,有 16 例(包括 MDS/MPD 和 14 例淋巴瘤)为供者源性;其余肿瘤的来源尚未确定。GVHD 预防、HLA 匹配、原发性疾病、年龄、总核细胞剂量和 CD34+细胞剂量与二次恶性肿瘤发生率无相关性。双 UCBT 后发生供者来源的二次髓系恶性肿瘤,提示应在所有怀疑复发的患者中进行供者来源的检测。

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