Tong Xiu-Zhen, Xu Duo-Rong, Zou Wai-Yi, Li Juan, Luo Shao-Kai, Peng Ai-Hua, Zhang Guo-Cai, Zheng Dong
Department of Hematology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 510080, PR China.
Ai Zheng. 2007 Aug;26(8):914-8.
BACKGROUND & OBJECTIVE: Busulfan (Bu) is commonly used as a component of conditioning regimens for hematopoietic stem cell transplantation. Erratic gastrointestinal absorption as a result of oral administration of Bu not only affects the efficacy, but also increases the risk of toxicity. This study was to analyze the efficacy and toxicity of intravenous Bu and cyclophosphamide (Cy) conditioning before allogeneic peripheral blood stem cell transplantation (allo-PBSCT) for leukemia.
Fifteen leukemia patients received intravenous Bu/Cy conditioning before allo-PBSCT, while 20 patients received oral Bu/Cy conditioning. The responses and adverse events of the 2 groups were assessed.
All 15 patients in intravenous Bu/Cy group had hematopoietic engraftment. The median time of engraftment was 12 (9-15) days for neutrophils and 15 (11-24) days for platelets. Of the 15 patients, 6 (40.0%) developed acute graft-versus-host disease (aGVHD), including 4 cases of grade I-II aGVHD and 2 cases of grade III-IV aGVHD; during conditioning, 7 (46.6%) had vomiting, 1 (6.7%) had oral mucositis, 1 (6.7%) had hemorrhagic cystitis, 2 (13.3%) had hepatic damage, none developed seizure. With a median follow-up of 180 days (range, 35-420 days), 14 (93.3%) patients were alive, 1 died of severe aGVHD accompanied fungal infection of the lung and central nerve system. The occurrence rates of hepatic damage and oral mucositis were significantly lower in intravenous Bu/Cy group than in oral Bu/Cy group (13.3% vs. 60.0%, 6.7% vs. 80.0%, P<0.01). There were no significant differences in hematopoietic reconstruction, aGVHD, stomatitis, gastrointestinal reaction, and hemorrhagic cystitis between the 2 groups (P>0.05).
The intravenous Bu/Cy conditioning before allo-PBSCT for leukemia has clear efficacy with low extramedullary toxicity.
白消安(Bu)常用于造血干细胞移植预处理方案。口服白消安导致的胃肠道吸收不稳定不仅影响疗效,还增加了毒性风险。本研究旨在分析静脉注射白消安联合环磷酰胺(Cy)预处理方案用于白血病异基因外周血干细胞移植(allo-PBSCT)的疗效及毒性。
15例白血病患者在allo-PBSCT前接受静脉注射Bu/Cy预处理,20例患者接受口服Bu/Cy预处理。评估两组的反应及不良事件。
静脉注射Bu/Cy组的15例患者均实现造血植入。中性粒细胞植入的中位时间为12(9-15)天,血小板植入的中位时间为15(11-24)天。15例患者中,6例(40.0%)发生急性移植物抗宿主病(aGVHD),其中4例为Ⅰ-Ⅱ级aGVHD,2例为Ⅲ-Ⅳ级aGVHD;预处理期间,7例(46.6%)出现呕吐,1例(6.7%)出现口腔黏膜炎,1例(6.7%)出现出血性膀胱炎,2例(13.3%)出现肝损伤,无患者发生癫痫。中位随访180天(范围35-420天),14例(93.3%)患者存活,1例死于严重aGVHD伴肺部及中枢神经系统真菌感染。静脉注射Bu/Cy组肝损伤和口腔黏膜炎的发生率显著低于口服Bu/Cy组(13.3% 对60.0%,6.7% 对80.0%,P<0.01)。两组在造血重建、aGVHD、口腔炎、胃肠道反应及出血性膀胱炎方面无显著差异(P>0.05)。
白血病allo-PBSCT前静脉注射Bu/Cy预处理疗效确切,髓外毒性低。