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A Modified Intensive Strategy to Prevent Cytomegalovirus Disease in Seropositive Umbilical Cord Blood Transplantation Recipients.
Hill, Joshua Aiden; Pergam, Steven A; Cox, Emily; Xie, Hu; Leisenring, Wendy M; Boeckh, Michael; Delaney, Colleen; Milano, Filippo.
Afiliação
  • Hill JA; Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington. Electronic address: jahill3@fredhutch.org.
  • Pergam SA; Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Cox E; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Xie H; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Leisenring WM; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Boeckh M; Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Delaney C; Department of Medicine, University of Washington, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Milano F; Department of Medicine, University of Washington, Seattle, Washington; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Biol Blood Marrow Transplant ; 24(10): 2094-2100, 2018 10.
Article em En | MEDLINE | ID: mdl-29753836
We previously demonstrated a lower rate of cytomegalovirus (CMV) reactivation and disease among seropositive umbilical cord blood transplantation (CBT) recipients receiving an intensive prophylaxis strategy consisting of ganciclovir on days -8 to -2 pretransplantation, high-dose valacyclovir post-transplantation, and twice-weekly serum CMV polymerase chain reaction testing. We hypothesized that a modified intensive strategy excluding pretransplantation ganciclovir would be similarly effective. We compared the risk of CMV reactivation, occurrence of CMV disease, and duration of anti-CMV therapy by day 100 post-CBT in patients receiving the modified intensive and intensive strategies. Forty patients received the modified intensive strategy, and 43 received the intensive strategy. There was no difference in the hazard for CMV reactivation (hazard ratio, 1.1; P = .77). No patients in the modified intensive cohort, but 2 patients in the intensive cohort, developed CMV disease (P = .53). There was no difference in the hazard for early (≤30 days post-CBT; P = .76) or high-level (>1000 IU/mL; P = .37) CMV reactivation. Patients in the modified intensive cohort had marginally higher CMV viral loads and percentage of days of CMV detection and treatment, although the contribution of pretransplantation ganciclovir to these differences is unclear. The overall percentage of treatment days was 32% in both cohorts after accounting for pretransplantation ganciclovir. In conclusion, exclusion of prophylactic ganciclovir before CBT did not impact the risk of CMV reactivation or disease, although CMV kinetics appeared to differ by prevention strategy. Best practices for CMV prevention will need further study as new prophylactic strategies become available.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ganciclovir / Infecções por Citomegalovirus / Citomegalovirus / Transplante de Células-Tronco de Sangue do Cordão Umbilical Tipo de estudo: Etiology_studies / Guideline Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Assunto da revista: HEMATOLOGIA / TRANSPLANTE Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ganciclovir / Infecções por Citomegalovirus / Citomegalovirus / Transplante de Células-Tronco de Sangue do Cordão Umbilical Tipo de estudo: Etiology_studies / Guideline Limite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Biol Blood Marrow Transplant Assunto da revista: HEMATOLOGIA / TRANSPLANTE Ano de publicação: 2018 Tipo de documento: Article