Chen Yuhong, Huang Xiaojun, Xu Lanping, Liu Daihong, Zhang Yaochen, Ren Hanyun, Guo Nailan, Lu Daopei
Hematological Institute, People's Hospital, Peking University, Beijing 100044, China.
Zhonghua Yi Xue Za Zhi. 2002 Oct 10;82(19):1306-9.
To study the feasibility and clinical outcome of granulocyte-colony stimulating factor (G-CSF) mobilized allogeneic bone marrow (G-BM) plus G-CSF mobilized peripheral blood stem cells (G-PBSC) transplantation for malignant hematological disease.
G-BM plus G-PBSC transplantation was conducted between siblings or between parent and child. G-CSF was injected hypodermically into 14 stem cell donors 5 micro g x kg(-1) x d(-1) for 4 approximately 6 days. On the 3rd day after beginning of G-CSF injection bone marrow blood was extracted from the posterior superior iliac spine of the donors; on the 4th day G-PBSCs were collected. The collected stem cells were transplanted immediately into the bodies of the 14 patients with hematological disease, including acute myelocytic leukemia, acute lymphocytic leukemia, multiple myeloma, myelodysplastic syndrome and severe aplastic anemia. The clinical outcomes, including the rate of engraftment, speed of engraftment, and the occurrence of acute graft versus host disease (aGVHD) and chronic graft versus host disease (cGVHD) were investigated.
All patients got endurable engraftment. The median time of recovery of neutrophil count to >or= 1 x 10(9)/L was 14 days (range 12 approximately 18 days). The median time to achieve a platelet count >or= 20 x 10(9)/L without transfusion was 13 days (range 11 approximately 65 days). Seven of the 14 patients developed aGVHD, 4 being in the grade I and 3 being in grade II. Three of the evaluable 9 patients developed extensive chronic GVHD. Two patients died of relapsed leukemia. One patient received secondary PBSCT from hte same donor because of ill engraftment and developed grade IV GVHD and died. The other 11 patients were still alive and event-free with a median follow-up duration of 455 days (range 84 approximately 715 days).
An effective treatment for malignant hematological disease, G-CSF mobilized allogeneic bone marrow plus peripheral blood stem cells transplantation provides rapid and sustained engraftment without increase in incidence of aGVHD and cGVHD.
研究粒细胞集落刺激因子(G-CSF)动员的异基因骨髓(G-BM)加G-CSF动员的外周血干细胞(G-PBSC)移植治疗恶性血液病的可行性及临床疗效。
在同胞间或亲子间进行G-BM加G-PBSC移植。对14例干细胞供者皮下注射G-CSF,剂量为5μg·kg⁻¹·d⁻¹,共4至6天。在开始注射G-CSF后的第3天,从供者双侧髂后上棘抽取骨髓血;第4天采集G-PBSC。将采集的干细胞立即输注到14例血液病患者体内,这些患者包括急性髓细胞白血病、急性淋巴细胞白血病、多发性骨髓瘤、骨髓增生异常综合征和重型再生障碍性贫血。观察临床疗效,包括植入率、植入速度以及急性移植物抗宿主病(aGVHD)和慢性移植物抗宿主病(cGVHD)的发生情况。
所有患者均获得持久植入。中性粒细胞计数恢复至≥1×10⁹/L的中位时间为14天(范围12至18天)。血小板计数在无输血情况下达到≥20×10⁹/L的中位时间为13天(范围11至65天)。14例患者中有7例发生aGVHD,其中Ⅰ度4例,Ⅱ度3例。9例可评估患者中有3例发生广泛慢性GVHD。2例患者死于白血病复发。1例患者因植入不佳接受了来自同一供者的二次外周血干细胞移植,发生Ⅳ度GVHD并死亡。其他11例患者仍存活且无事件发生,中位随访时间为455天(范围84至715天)。
G-CSF动员的异基因骨髓加外周血干细胞移植是治疗恶性血液病的一种有效方法,能实现快速且持久的植入,同时不增加aGVHD和cGVHD的发生率。