Risk and Predictive Factors for Candidemia After Allogeneic Hematopoietic Cell Transplantation: JS']JSTCT Transplant Complications Working Group

被引:4
作者
Kimura, Shun-ichi [1 ,24 ]
Kameda, Kazuaki [1 ,24 ]
Harada, Kaito [2 ,24 ]
Saburi, Masuho [3 ,24 ]
Okinaka, Keiji [4 ,5 ,24 ]
Shinohara, Akihito [6 ,24 ]
Uchida, Naoyuki [7 ]
Nishijima, Akihiko [8 ]
Ozawa, Yukiyasu [9 ]
Tanaka, Masatsugu [10 ]
Kuriyama, Takuro [11 ]
Katayama, Yuta [12 ,13 ]
Sawa, Masashi [14 ]
Ikegame, Kazuhiro [15 ]
Kawakita, Toshiro [16 ]
Kanda, Yoshinobu [1 ,17 ]
Nakamae, Hirohisa [18 ]
Ara, Takahide [19 ]
Kimura, Takafumi [20 ]
Sato, Atsushi [21 ]
Fukuda, Takahiro [5 ]
Atsuta, Yoshiko [22 ,23 ]
Nakasone, Hideki [1 ,24 ]
机构
[1] Jichi Med Univ, Div Hematol, Saitama Med Ctr, Saitama, Japan
[2] Tokai Univ, Dept Hematol & Oncol, Sch Med, Isehara, Kanagawa, Japan
[3] Oita Prefectural Hosp, Dept Hematol, Oita, Japan
[4] Natl Canc Ctr Hosp East, Dept Gen Med & Infect Dis, Chiba, Japan
[5] Natl Canc Ctr, Dept Hematopoiet Stem Cell Transplantat, Tokyo, Japan
[6] Tokyo Womens Med Univ, Dept Hematol, Tokyo, Japan
[7] Toranomon Gen Hosp, Dept Hematol, Federat Natl Publ Serv Personnel Mutual Aid Assoc, Tokyo, Japan
[8] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Hematol Div, Tokyo, Japan
[9] Japanese Red Cross Nagoya First Hosp, Dept Hematol, Nagoya, Aichi, Japan
[10] Kanagawa Canc Ctr, Dept Hematol, Yokohama, Kanagawa, Japan
[11] Hamanomachi Hosp, Dept Hematol, Fukuoka, Japan
[12] Hiroshima Red Cross Hosp, Dept Hematol, Hiroshima, Japan
[13] Atom Bomb Survivors Hosp, Hiroshima, Japan
[14] Anjo Kosei Hosp, Dept Hematol & Oncol, Anjo, Aichi, Japan
[15] Hyogo Coll Med Hosp, Dept Hematol, Nishinomiya, Hyogo, Japan
[16] Natl Hosp Org, Dept Hematol, Kumamoto Med Ctr, Kumamoto, Japan
[17] Jichi Med Univ, Div Hematol, Shimotsuke, Tochigi, Japan
[18] Osaka City Univ, Grad Sch Med, Hematol, Osaka, Japan
[19] Hokkaido Univ Hosp, Dept Hematol, Sapporo, Hokkaido, Japan
[20] Japanese Red Cross Kinki Block Blood Ctr, Preparat Dept, Osaka, Japan
[21] Miyagi Childrens Hosp, Dept Hematol & Oncol, Sendai, Miyagi, Japan
[22] Japanese Data Ctr Hematopoiet Cell Transplantat, Nagoya, Aichi, Japan
[23] Aichi Med Univ, Dept Registry Sci Transplant & Cellular Therapy, Sch Med, Nagoya, Aichi, Japan
[24] Japan Soc Transplantat & Cellular Therapy JSTCT, Transplant Complicat Working Grp, Nagoya, Aichi, Japan
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2022年 / 28卷 / 04期
关键词
Candidemia; Engraftment; Graft-versus-host disease; Hematopoietic cell transplantation-specific comorbidity index; Performance status; INVASIVE FUNGAL-INFECTIONS; ACUTE MYELOID-LEUKEMIA; VERSUS-HOST-DISEASE; COMORBIDITY INDEX; EUROPEAN ORGANIZATION; TRUMP DATA; RECIPIENTS; EPIDEMIOLOGY; MANAGEMENT; DONORS;
D O I
10.1016/j.jtct.2021.12.020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although antifungal prophylaxis that covers Candida species is a standard of care in allogeneic hematopoietic cell transplantation (HCT), candidemia mainly caused by non-albicans Candida species still occurs and is associated with a high mortality rate. This study aimed to evaluate the risk factors for candidemia after allogeneic HCT. Particularly, we evaluated the impact of patient factors such as hematopoietic cell transplantation-specific comorbidity index (HCT-CI) and performance status (PS) in addition to well-recognized risk factors including donor type, delayed engraftment, and graft-versus-host disease (GVHD). By using data from a Japanese transplant registry database, we analyzed 26,236 pediatric and adult patients with hematological malignancies who underwent their first allogeneic HCT. The posttransplant period was divided into early (days 0-40), late (days 41-100) and very late (days 101-365) phases. The 1-year cumulative incidence of candidemia was 1.8%. When we analyzed pretransplantation factors, age >40 years (hazard ratio [HR] 1.85), male (HR 1.34), HCT-CI (HCT-CI 1-2, HR 1.56; HCT-CI > 3, HR 2.21), PS > 2 (HR 2.01), high-risk disease (HR 1.78) and donor type including HLA-mismatched related donor (MMRD) (HR 1.96), HLA-mismatched unrelated donor (HR 2.05), and cord blood (CB) (HR 2.85) were significantly associated with an increased incidence of candidemia. Focusing on the early phase (days 0-40), HCT-CI, PS, high-risk disease and CB transplantation together with engraftment and severe acute GVHD signifi- cantly affected the development of candidemia. In the late phase (days 41-100), higher HCT-CI, male, and donor type including MMRD, and CB were associated with the occurrence of candidemia together with acute GVHD and disease relapse. In the very late phase (days 101-365), HCT-CI > 3 and high-risk disease significantly affected the occurrence of candidemia together with acute and chronic GVHD, and disease relapse. In addition to well-recognized risk factors including donor type, engraftment and GVHD, patient factors such as HCT-CI and PS were associated with the development of candidemia, which suggests that severely ill patients with transplantation-associated complications are more likely to develop candidemia. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
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收藏
页码:209.e1 / 209.e9
页数:9
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