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CMV reactivation during pretransplantation evaluation: a novel risk factor for posttransplantation CMV reactivation.
Zamora, Danniel; Xie, Hu; Sadowska-Klasa, Alicja; Kampouri, Eleftheria; Biernacki, Melinda A; Ueda Oshima, Masumi; Duke, Elizabeth; Green, Margaret L; Kimball, Louise E; Holmberg, Leona; Waghmare, Alpana; Greninger, Alexander L; Jerome, Keith R; Hill, Geoffrey R; Hill, Joshua A; Leisenring, Wendy M; Boeckh, Michael J.
Afiliação
  • Zamora D; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Xie H; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Sadowska-Klasa A; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Kampouri E; Department of Hematology and Transplantology, Medical University of Gdansk, Gdansk, Poland.
  • Biernacki MA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Ueda Oshima M; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Duke E; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Green ML; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Kimball LE; Division of Allergy & Infectious Disease, University of Washington School of Medicine, Seattle, WA.
  • Holmberg L; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Waghmare A; Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Greninger AL; Department of Pediatrics, University of Washington School of Medicine, Seattle, WA.
  • Jerome KR; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Hill GR; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA.
  • Hill JA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
  • Leisenring WM; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, WA.
  • Boeckh MJ; Translational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA.
Blood Adv ; 8(17): 4568-4580, 2024 Sep 10.
Article em En | MEDLINE | ID: mdl-38924728
ABSTRACT
ABSTRACT Cytomegalovirus (CMV) disease occurs occasionally before allogeneic hematopoietic cell transplantation (HCT) and is associated with poor post-HCT outcomes; however, the impact of pre-HCT CMV reactivation is unknown. Pre-HCT CMV reactivation was assessed in HCT candidates from the preemptive antiviral therapy (2007-2017) and letermovir prophylaxis (2018-2021) eras. CMV DNA polymerase chain reaction (PCR) surveillance was routinely performed during the pre-HCT workup period, and antiviral therapy was recommended according to risk of progression to CMV disease. Risk factors for pre-HCT CMV reactivation were characterized, and the associations of pre-HCT CMV reactivation with post-HCT outcomes were examined using logistic regression and Cox proportional hazard models, respectively. A total of 1694 patients were identified, and 11% had pre-HCT CMV reactivation 14 days (median; interquartile range [IQR], 6-23) before HCT. Lymphopenia (≤0.3 × 103/µL) was the strongest risk factor for pre-HCT CMV reactivation at multiple PCR levels. In the preemptive therapy era, patients with pre-HCT CMV reactivation had a significantly increased risk of CMV reactivation by day 100 as well as CMV disease and death by 1 year after HCT. Clearance of pre-HCT CMV reactivation was associated with a lower risk of post-HCT CMV reactivation. Similar associations with post-HCT CMV end points were observed in a cohort of patients receiving letermovir prophylaxis. Pre-HCT CMV reactivation can be routinely detected in high-risk HCT candidates and is a significant risk factor for post-HCT CMV reactivation and disease. Pre-HCT CMV DNA PCR surveillance is recommended in high-risk HCT candidates, and antiviral therapy may be indicated to prevent post-HCT CMV reactivation.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article