Clinical Impact of BK Viremia during Haploidentical Stem Cell Transplantation and Its Association with Hemorrhagic Cystitis

Author:

Xu Lan-Ping1ORCID,Chen Yao2,Zhao Xiaosu3ORCID,Chen Huan4,Lv Meng5,Fu Haixia6,Chen Yuhong1,Wang Feng-Rong7,Jingzhi Wang1,Yan Chen-Hua8,Zhang Yuan-Yuan1,Mo Xiao-Dong1ORCID,Zhang Xiaohui1ORCID,Wang Yu9ORCID,Huang XiaoJun1

Affiliation:

1. Peking University People's Hospital

2. Peiking University Institute of Hematology

3. Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplan

4. Department of Hematology,People's Hospital

5. Peking University People's Hospital, Peking University Institute of Hematology

6. Peking University People's Hospital, Peking University Institute of Hematology; National Clinical Research Center for Hematologic Disease; Collaborative Innovation Center of Hematology

7. Peking University Institute of Hematology, People's hospital

8. Peking University People's Hosital, Peking University Institute of Hematology

9. Peking University People’s Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Tr

Abstract

Abstract Few studies have explored the clinical impact of BK virus DNAemia on haploidentical stem cell transplantation (SCT). Therefore, we retrospectively analyzed the clinical impact of BK DNAemia on haploidentical SCT between 2021 and 2023. In total, 278 patients were enrolled. BKV DNA in plasma was positive in 54 (19.4%) patients, the median time to onset was 35 days (range, 12–385) after transplantation, and the median blood BK viral load was 4970 copies/ml (191-5.04E + 9). The incidence of hemorrhagic cystitis (HC), including severe cases, was significantly higher in the BK-positive group compared to the BK-negative patients (77.8% vs. 20.5%, P < 0.001; 27.8% vs. 10.3%, P < 0.001). Receiver operating characteristic curve analysis revealed that a blood BKV-DNA load > 0 copies/ml had a sensitivity of 47.13% and a specificity of 93.68% for predicting HC (P < 0.0001). A BKV-DNA load > 191 copies/ml exhibited a sensitivity of 60.53% and a specificity of 87.87% for predicting severe HC (P < 0.0001). BK viremia is prevalent among haploidentical transplant recipients. Moreover, these findings suggest that BK viremia serves as an early indicator of HC development.

Publisher

Research Square Platform LLC

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