BK Virus-Hemorrhagic Cystitis Following Allogeneic Stem Cell Transplantation: Clinical Characteristics and Utility of Leflunomide Treatment

被引:0
作者
Park, Young Hoon [1 ]
Lim, Joo Han [1 ]
Yi, Hyeon Gyu [1 ]
Lee, Moon Hee [1 ]
Kim, Chul Soo [1 ]
机构
[1] Inha Univ, Fac Med & Hosp, Dept Hematol Oncol, Inchon, South Korea
关键词
BK virus; Hemorrhagic cystitis; Allogeneic stem cell transplantation; Leflunomide; BONE-MARROW-TRANSPLANTATION; DIFFERENT RISK-FACTORS; RENAL-TRANSPLANTATION; RECIPIENTS; CIDOFOVIR; NEPHROPATHY; MANAGEMENT; INFECTION; CHILDREN; ASSOCIATION;
D O I
10.4274/tjh.2015.0131
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: BK virus-hemorrhagic cystitis (BKV-HC) is a potential cause of morbidity and mortality in patients having undergone allogeneic stem cell transplantation (Allo-SCT). We analyzed the clinical features of BKV-HC following Allo-SCT and reported the utility of leflunomide therapy for BKV-HC. Materials and Methods: From January 2005 to June 2014, among the 69 patients that underwent Allo-SCT in our institution, the patients who experienced BKV-HC were investigated retrospectively. Results: HC was observed in 30 patients (43.5%), and among them, 18 of the cases (26.1%) were identified as BKV-HC. The median age of the patients (12 males and 6 females) was 45 years (minimum-maximum: 13-63). Patients received Allo-SCT for acute myeloid leukemia (n=11), aplastic anemia (n=4), myelodysplastic syndrome (n=2), and non-Hodgkin lymphoma (n=1). The donor types were human leukocyte antigen (HLA)-matched sibling donor for six patients, HLA-matched unrelated donor for nine, and haploidentical familial donor for two. The median onset and duration of BKV-HC was on day 21 after transplantation (minimum-maximum: 7-97) and 22 days (minimum-maximum: 6-107). Eleven patients (62.1%) had grade I-II HC and seven patients (38.9%) had grade III-IV (high-grade) HC. Among the seven patients who had high-grade HC, one had complete response, one had partial response, and five had no response. Among the five nonresponders, one died of BKV-HC associated complications. The remaining four patients were treated with leflunomide, achieving complete response (n=2) and partial response (n=2). The median duration from the start of leflunomide therapy to response was 13 days (minimum-maximum: 8-17 days). All patients tolerated the leflunomide treatment well, with three patients having mild gastrointestinal symptoms, including anorexia and abdominal bloating. Conclusion: BKV-HC was commonly observed in patients with HC following Allo-SCT. In high-grade BKV-HC patients who do not respond to supportive care, leflunomide may be a feasible option without significant toxicity.
引用
收藏
页码:223 / 230
页数:8
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