Heterogeneous impact of cytomegalovirus reactivation on nonrelapse mortality in hematopoietic stem cell transplantation

被引:25
|
作者
Kaito, Satoshi [1 ]
Nakajima, Yujiro [2 ,3 ]
Hara, Konan [1 ,4 ]
Toya, Takashi [1 ]
Nishida, Tetsuya [5 ]
Uchida, Naoyuki [6 ]
Mukae, Junichi [1 ]
Fukuda, Takahiro [7 ]
Ozawa, Yukiyasu [8 ]
Tanaka, Masatsugu [9 ]
Ikegame, Kazuhiro [10 ]
Katayama, Yuta [11 ,12 ]
Kuriyama, Takuro [13 ]
Kanda, Junya [14 ]
Atsuta, Yoshiko [15 ,16 ]
Ogata, Masao [17 ]
Taguchi, Ayumi [18 ]
Ohashi, Kazuteru [1 ]
机构
[1] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Hematol Div, Tokyo, Japan
[2] Tokyo Metropolitan Komagome Hosp, Dept Radiat Oncol, Tokyo, Japan
[3] Tohoku Univ, Radiat Oncol, Grad Sch Med, Sendai, Miyagi, Japan
[4] Univ Tokyo, Grad Sch Econ, Tokyo, Japan
[5] Nagoya Univ, Dept Hematol & Oncol, Grad Sch Med, Nagoya, Aichi, Japan
[6] Federat Natl Publ Serv Personnel Mutual Aid Assoc, Dept Hematol, Tokyo, Japan
[7] Natl Canc Ctr, Dept Hematopoiet Stem Cell Transplantat, Tokyo, Japan
[8] Japanese Red Cross Nagoya First Hosp, Dept Hematol, Nagoya, Aichi, Japan
[9] Kanagawa Canc Ctr, Dept Hematol, Yokohama, Kanagawa, Japan
[10] Hyogo Coll Med, Dept Internal Med, Div Hematol, Nishinomiya, Hyogo, Japan
[11] Hiroshima Red Cross Hosp, Dept Hematol, Hiroshima, Japan
[12] Atom Bomb Survivors Hosp, Hiroshima, Japan
[13] Hamanomachi Hosp, Dept Hematol, Fukuoka, Japan
[14] Kyoto Univ, Grad Sch Med, Dept Hematol & Oncol, Kyoto, Japan
[15] Japanese Data Ctr Hematopoiet Cell Transplantat, Nagoya, Aichi, Japan
[16] Nagoya Univ, Dept Healthcare Adm, Grad Sch Med, Nagoya, Aichi, Japan
[17] Oita Univ Hosp, Dept Hematol, Oita, Japan
[18] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Gynecol Div, Tokyo, Japan
关键词
BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; ACUTE MYELOID-LEUKEMIA; NON-RELAPSE MORTALITY; GANCICLOVIR PROPHYLAXIS; CMV REACTIVATION; RISK-FACTORS; T-CELLS; INFECTION; RECIPIENTS;
D O I
10.1182/bloodadvances.2019000814
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytomegalovirus (CMV) infection is a major complication in allogeneic stem cell transplantation. The utility of CMV prophylaxis with letermovir has been reported; however, the specific applications remain unclear. In this study, we retrospectively analyzed large-scale registry data (N = 10480) to clarify the risk factors for nonrelapse mortality (NRM) in connection with CMV reactivation. First, we identified risk factors for CMV reactivation using multivariate analysis and developed a scoring model. Although the model effectively stratified reactivation risk into 3 groups (43.7% vs 60.9% vs 71.5%; P < .001), the 3-year NRM was significantly higher in patients with CMV reactivation, even in the low (20.9% vs 13.0%, P < .001), intermediate (21.4% vs 15.6%; P < .001), and high (29.3% vs 18.0%; P < .001) reactivation risk groups. Next, survival analysis considering competing risks, time-dependent covariates, and interaction terms for exploring the heterogeneous impact of CMV reactivation on NRM in the training cohort revealed that chronic myeloid leukemia (CML) (hazard ratio [HR], 1.76; 95% confidence interval [CI], 1.05-2.96; P = .033), good performance status (PS) (HR, 1.42; 95% CI, 1.04-1.94; P = .028), HLA-matched donor (HR, 1.34; 95% CI, 1.06-1.70; P = .013), and standard-risk disease (HR, 1.28; 95% CI, 1.04-1.58; P = .022) were associated with increased NRM. In the test cohort, CMV reactivation was significantly associated with S increased 3-year NRM among patients with 2 to 4 factors (22.1% vs 13.1%; P < .001) but was comparable among patients with 0 or 1 factor (23.2% vs 20.4%; P = .62). We propose that CMV prophylaxis should be determined based on reactivation risk, as well as these other factors.
引用
收藏
页码:1051 / 1061
页数:11
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