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造血干细胞移植后出血性膀胱炎:发病率、危险因素以及与巨细胞病毒再激活和移植物抗宿主病的关联

Hemorrhagic cystitis following hematopoietic stem cell transplantation: incidence, risk factors and association with CMV reactivation and graft-versus-host disease.

作者信息

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

机构信息

Peking University Institute of Hematology, Peking University People's Hospital, Beijing 100044, China.

出版信息

Chin Med J (Engl). 2007 Oct 5;120(19):1666-71.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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