Bogdanovic Gordana, Priftakis Peter, Giraud Geraldine, Dalianis Tina
Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Anticancer Res. 2006 Mar-Apr;26(2B):1311-8.
The significance of the BK virus (BKV) and possible co-factors for the development of late onset haemorrhagic cystitis (HC) in allogeneic haematopoetic stem cell (HSCT)-transplanted patients is reviewed. BKV-associated HC causes significant morbidity and mortality in HSCT patients, however, BK-viruria cannot distinguish patients at risk of HC, since it is observed in patients with and without HC. Several studies have therefore attempted to identify co-factors for the development of HC. Acute graft versus host disease was in the past, though less so recently, reported to correlate to the incidence of HC. However, patients who had received grafts from unrelated donors (URD) and had had full conditioning prior to HSCT were shown to have an increased risk of HC, compared to patients who had received HSCT from a related donor (RD) or patients who had received reduced intensity conditioning. In conclusion, HSCT patients with BK-viruria, an URD and receiving full conditioning have an increased risk of developing HC.
本文综述了BK病毒(BKV)的意义以及同种异体造血干细胞移植(HSCT)患者发生迟发性出血性膀胱炎(HC)的可能协同因素。BKV相关的HC在HSCT患者中会导致显著的发病率和死亡率,然而,BK病毒尿症无法区分有HC风险的患者,因为在有和没有HC的患者中均能观察到。因此,多项研究试图确定HC发生的协同因素。过去曾报道急性移植物抗宿主病与HC的发生率相关,不过近年来这种相关性有所降低。然而,与接受相关供体(RD)的HSCT患者或接受减低强度预处理的患者相比,接受无关供体(URD)移植且在HSCT前接受了充分预处理的患者发生HC的风险增加。总之,有BK病毒尿症、接受URD且接受充分预处理的HSCT患者发生HC的风险增加。