Cytomegalovirus antigenemia and outcome of patients treated with pre-emptive ganciclovir: retrospective analysis of 241 consecutive patients undergoing allogeneic hematopoietic stem cell transplantation

被引:54
|
作者
Yanada, M
Yamamoto, K
Emi, N
Naoe, T
Suzuki, R
Taji, H
Iida, H
Shimokawa, T
Kohno, A
Mizuta, S
Maruyama, F
Wakita, A
Kitaori, K
Yano, K
Hamaguchi, M
Hamajima, N
Morishima, Y
Kodera, Y
Sao, H
Morishita, Y
机构
[1] Nagoya Univ, Grad Sch Med, Dept Hematol, Showa Ku, Aichi 4668550, Japan
[2] Aichi Canc Ctr, Dept Mol Med, Nagoya, Aichi 464, Japan
[3] Aichi Canc Ctr, Dept Hematol & Chemotherapy, Nagoya, Aichi 464, Japan
[4] Meitetsu Hosp, Dept Hematol, Nagoya, Aichi, Japan
[5] Nagoya Ekisaikai Hosp, Dept Internal Med, Nagoya, Aichi, Japan
[6] JA Aichi Showa Hosp, Dept Hematol & Oncol, Kohnan, Japan
[7] Anjo Kosei Hosp, Dept Hematol, Anjo, Japan
[8] Fujita Hlth Univ, Dept Hematol, Toyoake, Aichi, Japan
[9] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Nagoya, Aichi, Japan
[10] Japanese Red Cross Nagoya First Hosp, Dept Hematol, Nagoya, Aichi, Japan
[11] Hamamatsu Med Ctr, Dept Infect Dis, Hamamatsu, Shizuoka, Japan
[12] Nagoya Natl Hosp, Dept Hematol, Nagoya, Aichi, Japan
[13] Nagoya Natl Hosp, Clin Res Ctr, Nagoya, Aichi, Japan
[14] Nagoya Univ, Grad Sch Med, Dept Prevent Med Biostat & Med Decis Making, Nagoya, Aichi, Japan
关键词
cytomegalovirus; antigenemia; pre-emptive therapy; ganciclovir; hematopoietic stem cell transplantation;
D O I
10.1038/sj.bmt.1704232
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
CMV disease remains a major infectious complication after allogeneic hematopoietic stem cell transplantation (HSCT). To investigate the relationship between CMV antigenemia, treatment with ganciclovir (GCV), and outcome, we retrospectively analyzed 241 consecutive patients at risk for CMV infection who underwent allogeneic HSCT. Antigenemia-guided pre-emptive strategy with GCV was used for all patients. CMV antigenemia developed in 169 patients (70.1%), and CMV disease in 18 patients (7.5%). Multivariate analysis showed that acute GVHD (grades II-IV) was the only risk factor for developing antigenemia, and acute GVHD and advanced age for CMV disease. GCV use, as well as acute GVHD and advanced age, significantly increased the risk for bacterial and fungal infection after engraftment. Those who developed CMV antigenemia had a poorer outcome than those who did not (log-rank, P = 0.0269), although the development of CMV disease worsened the outcome with only borderline significance (log-rank, P = 0.0526). In conclusion, detection of antigenemia proved to be a poor prognostic factor for HSCT patients, which may be attributed to a combination of factors, including CMV disease itself, the effect of treatment, and a host status that allows for reactivation of CMV. Optimal pre-emptive strategy needs to be determined.
引用
收藏
页码:801 / 807
页数:7
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