Xu Lan-ping, Zhang Hong-yu, Huang Xiao-jun, Liu Kai-yan, Liu Dai-hong, Han Wei, Chen Huan, Chen Yu-hong, Gao Zhi-yong, Zhang Yao-chen, Lu Dao-pei
Peking University Institute of Hematology, Peking University People's Hospital, Beijing 100044, China.
Chin Med J (Engl). 2007 Oct 5;120(19):1666-71.
The definite pathogenesis of hemorrhagic cystitis (HC) after allogenic hematopoietic stem cell transplantation (allo-HSCT) has not been well elucidated. The role of cytomegalovirus (CMV) reactivation and graft-versus-host disease (GVHD) in the development of HC remains obscure. This study determined the incidence and risk factors for HC after allo-HSCT and analyzed its association with CMV reactivation and GVHD.
We retrospectively studied 250 patients at high risk for CMV disease who underwent allo-HSCT all based on busulfan/cyclophosphamide (BU/CY) myloablative regimens. The incidence, etiology, risk factors and clinical management of HC were investigated.
HC developed within 180 days of transplant in 72 patients, with an overall incidence of 28.8% and an incidence of 12.6% in patients with HLA-matched related donors (MRD), 34.38% in those with HLA-matched unrelated donors (MUD), 49.45% in those with mismatched related donors (MMRD). CMV-viremia significantly increased the incidence of later onset HC (LOHC); however, only 9 out of 15 patients with CMV viruria actually developed LOHC. Multiple regression analysis identified grade II - IV acute GVHD (RR = 2.75; 95% CI 1.63 +/- 4.66; P < 0.01) and grafts from MUD or MMRD (RR = 2.60; 95% CI 1.52 +/- 5.20; P < 0.01) as independent risk factors for HC. Event sequence analysis indicated a majority of HC episodes began around GVHD initiation.
CMV-viremia is a high risk factor for LOHC. Our data also showed a correlation between acute GVHD and HC, which suggested that alloimmunity may be involved in the pathogenesis of HC.
异基因造血干细胞移植(allo-HSCT)后出血性膀胱炎(HC)的确切发病机制尚未完全阐明。巨细胞病毒(CMV)再激活和移植物抗宿主病(GVHD)在HC发生发展中的作用仍不明确。本研究确定了allo-HSCT后HC的发生率和危险因素,并分析了其与CMV再激活和GVHD的关系。
我们回顾性研究了250例有CMV疾病高风险且均接受基于白消安/环磷酰胺(BU/CY)清髓方案的allo-HSCT患者。对HC的发生率、病因、危险因素及临床处理进行了调查。
72例患者在移植后180天内发生HC,总体发生率为28.8%,人类白细胞抗原(HLA)匹配的相关供者(MRD)患者发生率为12.6%,HLA匹配的无关供者(MUD)患者发生率为34.38%,HLA不匹配的相关供者(MMRD)患者发生率为49.45%。CMV病毒血症显著增加迟发性HC(LOHC)的发生率;然而,15例CMV病毒尿患者中只有9例实际发生了LOHC。多因素回归分析确定II-IV级急性GVHD(相对危险度RR = 2.75;95%可信区间CI 1.63±4.66;P < 0.01)以及来自MUD或MMRD的移植物(RR = 2.60;95%CI 1.52±5.20;P < 0.01)为HC的独立危险因素。事件序列分析表明,大多数HC发作始于GVHD开始时。
CMV病毒血症是LOHC的高危因素。我们的数据还显示急性GVHD与HC之间存在相关性,这表明同种免疫可能参与了HC的发病机制。