Use of granulocyte-macrophage colony-stimulating factor in two children treated with cord blood transplantation.

Blood cells Pub Date : 1994-01-01
M R Vowels, K Tiedemann, R Lam-Po-Tang, D P Tucker
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Abstract

Cord blood contains stem cells in amounts similar to or slightly less than those present in a bone marrow collection to be used for bone marrow transplantation (BMT). Too few cord blood transplants (CBT) have yet been performed to define the ability to achieve engraftment and the rate of engraftment. Two cord blood transplants have been performed using granulocyte-macrophage colony stimulating factor (GM-CSF) to hasten engraftment. Two children, aged 5 and 6 years received a CBT using HLA-identical stem cells collected at the birth of a sibling. One child had X-linked lymphoproliferative disease (XLP), and the other, acute lymphoblastic leukemia in second complete remission. One had an ABO and one an Rh blood group mismatch. Conditioning therapy consisted of cyclophosphamide, melphalan, and antithymocyte globulin or busulphan and cyclophosphamide. Graft-versus-host disease prophylaxis was methotrexate and cyclosporine or cyclosporine. Both children were given GM-CSF at 5 micrograms/kg/day from day 1 until the absolute neutrophil count (ANC) reached 1.0 x 10(9)/L for 3 consecutive days. If this level was not reached by day 14, the dose of GM-CSF was doubled. Both children engrafted rapidly, with ANCs reaching 0.5 x 10(9)/L in 12 and 16 days. Engraftment was confirmed by blood group in both and sex chromosome typing in one. Both children developed mild GVHD localized to skin, which resolved with steroid therapy. The child with XLP was cured and has survived for 34 months; the second child has survived 27 months with normal marrow function but has had a relapse of leukemia.(ABSTRACT TRUNCATED AT 250 WORDS)

粒细胞-巨噬细胞集落刺激因子在儿童脐带血移植中的应用。
脐带血中含有的干细胞数量与用于骨髓移植(BMT)的骨髓中含有的干细胞数量相似或略少。脐带血移植(CBT)的数量太少,无法确定移植的能力和移植的比率。两例脐带血移植使用粒细胞-巨噬细胞集落刺激因子(GM-CSF)来加速移植。两名年龄分别为5岁和6岁的儿童接受了CBT治疗,使用的是在其兄弟姐妹出生时收集的hla相同的干细胞。一名儿童患有x连锁淋巴细胞增生性疾病(XLP),另一名患有急性淋巴细胞白血病,第二次完全缓解。一个ABO血型和一个Rh血型不匹配。调理治疗包括环磷酰胺、美伐兰和抗胸腺细胞球蛋白或丁硫芬和环磷酰胺。预防移植物抗宿主病的方法是甲氨蝶呤和环孢素或环孢素。两例患儿从第1天开始给予GM-CSF 5微克/千克/天,直至绝对中性粒细胞计数(ANC)达到1.0 × 10(9)/L,连续3天。如果到第14天还没有达到这个水平,GM-CSF的剂量加倍。两例患儿植皮迅速,12、16天的ANCs均达到0.5 × 10(9)/L。经血型鉴定和性染色体分型鉴定均证实移植。这两个孩子都出现了轻度的局部皮肤GVHD,用类固醇治疗后消退。患有XLP的儿童被治愈并存活了34个月;第二个孩子存活了27个月,骨髓功能正常,但白血病复发。(摘要删节250字)
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