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Infection-related mortality after HLA-identical and haploidentical hematopoietic cell transplantation using reduced-intensity conditioning in an outpatient setting
被引:8
|作者:
Carlos Jaime-Perez, Jose
[1
,2
]
Melendez-Flores, Jesus D.
[1
,2
]
Ramos-Davila, Eugenia M.
[1
,2
]
Gutierrez-Aguirre, Cesar Homero
[1
,2
]
Cantu-Rodriguez, Olga G.
[1
,2
]
Javier Marfil-Rivera, Luis
[1
,2
]
Ancer-Rodriguez, Jesus
[3
]
Gomez-Almaguer, David
[1
,2
]
机构:
[1] Univ Autonoma Nuevo Leon, Dr Jose Eleuterio Gonzalez Univ Hosp, Hematol Dept, Internal Med Div, Monterrey, Mexico
[2] Univ Autonoma Nuevo Leon, Sch Med, Monterrey, Mexico
[3] Univ Autonoma Nuevo Leon, Sch Med, Pathol Dept, Monterrey, Mexico
关键词:
allogeneic hematopoietic cell transplantation;
haploidentical hematopoietic cell transplantation;
infectious diseases;
infectious complications;
post-transplant cyclophosphamide;
POSTTRANSPLANTATION CYCLOPHOSPHAMIDE;
MARROW-TRANSPLANTATION;
FUNGAL-INFECTIONS;
RISK-FACTORS;
DISEASE;
COMPLICATIONS;
BACTERIAL;
OUTCOMES;
D O I:
10.1111/ctr.14972
中图分类号:
R61 [外科手术学];
学科分类号:
摘要:
Background: Despite the improvements in supportive care for allogeneic-hematopoietic cell transplantation (allo-HCT) recipients, infectious complications and infection-related mortality (IRM) continue to be a major issue for transplantation centers. Methods: We herein report the infectious complications and IRM of 107 and 89 patients that underwent haploidentical (haplo-HCT) or HLA-identical HCT at a tertiary referral center during 2013-2020. Patients in the haplo-HCT group received post-transplant cyclophosphamide (PT-Cy), and all received reduced-intensity conditioning regimens. Results: More haplo-HCT recipients presented severe infections in the pre-engraftment period (22.4% vs. 6.7%, p = 0.003). Viral (14.9% vs. 4.5%, p = 0.016) and fungal (12.1% vs. 1.1%, p = 0.003) etiologies were more common in this period in this group. The 100-day and 2-year cumulative incidence of IRM was 15% and 21% for the haplo-HCT and 5.6% and 17% for the HLA-identical group; no significant differences were observed between the groups. Fungal pathogens mainly contributed to IRM (33.3%). Infections were the most common cause of mortality (40/81, 49.4%). There were significant differences in donor/recipient CMV serostatus between transplant groups (0.002). Conclusions: No differences in IRM were observed based on allo-HCT type, with more haplo-HCT patients suffering from severe infections in the pre-engraftment period. Studies to assess future prevention, diagnostic, and treatment strategies to reduce IRM are warranted.
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页数:10
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