Tang Xiang-Feng, Luan Zuo, Xu Shi-Xia, Wu Nan-Hai, Huang You-Zhang, Wang Kai
Department of Pediatrics, Navy General Hospital of People's Liberation Army, Beijing 100037, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2008 Feb;10(1):5-8.
Unrelated umbilical cord blood has the clear benefits of rapid availability and a reduced stringency of requirement for HLA match. The aim of this study was to investigate the efficacy of unrelated umbilical cord blood transplantation (UCBT) in the treatment of malignant leukemia in children.
Six children with malignant leukemia, including three cases of acute lymphocyte leukemia [two high-risk patients and one standard-risk patient in complete remission (CR)], two juvenile myelomonocytic leukemia (one in CR and one in the accelerating stage), and one acute myeloblastic leukaemia (in CR), received a UCBT. The umbilical cord blood grafts were HLA-matched (n=1) or HLA-mismatched at 1 (n=1) or 2 (n=1) or 3 (n=3) loci. Busulfan/cyclophosphamide/antithymocyte globulin (ATG) or total body irradiation (TBI)/cyclophosphamide/ATG was involved in the myeloablative pretreatment regimen. The median infused donor nucleated cell was 8.51 x 10(7)/kg of recipient weight, and the CD34+ cell was 1.81 x 10(5)/kg of recipient weight. Cyclosporin, corticoid, mycophenolate mofetil and daclizumab were used for prophylaxis of acute graft versus host disease (GVHD).
The time to reach an absolute neutrophil count of 0.5 x 10(9)/L ranged from 11 to 35 days (median: 13 days) and the time to reach a platelet count of 20 x 10(9)/L ranged from 27 to 68 days (median: 30 days) after transplantation, and the donors' hematopoietic stem cells were shown in these patients. Four patients developed grade I to III acute GVHD but responded to steroids and daclizumab. Chronic GVHD was not found during a 3-16-month follow-up. Four patients survived and did not relapse during the follow-up.
Unrelated umbilical cord blood is an alternative source of hematopoietic stem cells for patients with leukemia. UCBT can tolerate 1-2 HLA mismatches. The incidence of acute GVHD is high in UCBT recipients.
非亲属脐血具有快速可得以及对人类白细胞抗原(HLA)配型要求宽松的明显优势。本研究旨在探讨非亲属脐血移植(UCBT)治疗儿童恶性白血病的疗效。
6例恶性白血病患儿接受了UCBT,其中包括3例急性淋巴细胞白血病[2例高危患者和1例处于完全缓解(CR)期的标危患者]、2例青少年粒单核细胞白血病(1例处于CR期,1例处于加速期)以及1例急性髓细胞白血病(处于CR期)。脐血移植物HLA配型相合的有1例,1个位点不相合的有1例,2个位点不相合的有1例,3个位点不相合的有3例。清髓预处理方案采用白消安/环磷酰胺/抗胸腺细胞球蛋白(ATG)或全身照射(TBI)/环磷酰胺/ATG。输注的供体有核细胞中位数为8.51×10⁷/kg受者体重,CD34⁺细胞为1.81×10⁵/kg受者体重。使用环孢素、皮质类固醇、霉酚酸酯和达利珠单抗预防急性移植物抗宿主病(GVHD)。
移植后达到绝对中性粒细胞计数0.5×10⁹/L 的时间为11至35天(中位数:13天),达到血小板计数20×10⁹/L 的时间为27至68天(中位数:30天),且在这些患者中显示出供体造血干细胞。4例患者发生了Ⅰ至Ⅲ级急性GVHD,但对类固醇和达利珠单抗有反应。在3至16个月的随访期间未发现慢性GVHD。4例患者存活且在随访期间未复发。
非亲属脐血是白血病患者造血干细胞的替代来源。UCBT可耐受1至2个HLA位点不相合。UCBT受者急性GVHD的发生率较高。