Prophylactic Foscarnet for Human Herpesvirus 6: Effect on Hematopoietic Engraftment after Reduced-Intensity Conditioning Umbilical Cord Blood Transplantation
Autor: | Najla El Jurdi, John Rogosheske, Shernan G. Holtan, Brian C. Betts, Nelli Bejanyan, Veronika Bachanova, Joseph Maakaron, Armin Rashidi, Erica D. Warlick, Murali Janakiram, Samantha Larson, Todd E. DeFor, John E. Wagner, Claudio G. Brunstein, Daniel J. Weisdorf, Fiona He, Jo Anne H. Young, Mukta Arora |
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Rok vydání: | 2021 |
Předmět: |
Foscarnet
medicine.medical_specialty Herpesvirus 6 Human Graft vs Host Disease Gastroenterology Umbilical cord Article 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Humans Immunology and Allergy Cumulative incidence Transplantation Neutrophil Engraftment Umbilical Cord Blood Transplantation business.industry Hematopoietic Stem Cell Transplantation virus diseases Cell Biology Hematology biochemical phenomena metabolism and nutrition Total body irradiation Fludarabine medicine.anatomical_structure 030220 oncology & carcinogenesis Molecular Medicine Cord Blood Stem Cell Transplantation business 030215 immunology medicine.drug |
Zdroj: | Transplant Cell Ther |
ISSN: | 2666-6367 |
DOI: | 10.1016/j.bbmt.2020.10.008 |
Popis: | The high incidence of human herpesvirus-6 (HHV-6) reactivation, potentially interfering with engraftment after umbilical cord blood (UCB) hematopoietic cell transplantation (HCT), remains a major challenge. To potentially address this problem, we evaluated the effect of prophylactic foscarnet administered twice daily beginning on day +7 and continuing through engraftment in 25 patients. To determine the impact of foscarnet on HHV-6, engraftment, and other transplantation outcomes, we compared results in 61 identically treated patients with hematologic malignancies. Treatment and control groups underwent reduced-intensity conditioning UCB HCT with a conditioning regimen of fludarabine, cyclophosphamide, and total body irradiation 200 cGy with or without antithymocyte globulin (ATG), using sirolimus plus mycophenolate mofetil immune suppression. The treatment and control groups were similar in terms of age, disease risk, use of ATG, Hematopoietic Cell Transplantation Comorbidity Index, and graft CD34 cell dose; however, foscarnet-treated patients were less likely to receive a double UCB graft and to be treated more recently (2016 to 2018). The cumulative incidence of HHV-6 reactivation by day +100 was 63% for all patients (95% confidence interval [CI], 51% to 75%) and was not significantly different between the 2 groups. HHV-6 reactivation occurred at a median of 34 days in the foscarnet group and 25.5 days in the control group. The incidence of neutrophil engraftment at day 42 was higher in the foscarnet group compared with the control group (96%; [95% CI, 83% to 100%] versus 75% [95% CI, 64% to 85%]; P< .01). The cumulative incidence of platelet engraftment by 6 months was 92% (95% CI, 69% to 100%) for the foscarnet group versus 75% (95% CI, 60% to 90%) for the control group (P= .08), and multivariate analysis identified the use of foscarnet as an independent predictor of better platelet engraftment. No patients died as a result of graft failure in recipients of foscarnet, whereas 5 patients died from graft failure in the control group. Six-month overall survival (OS) and nonrelapse mortality (NRM) were better in the foscarnet group (96% versus 72% [P= .02] and 4% versus 18% [P= .07], respectively). Even though foscarnet prophylaxis did not prevent HHV-6 viremia, we observed a delay in time to HHV-6 reactivation, a trend toward differences in engraftment, NRM, and OS compared with historical controls. |
Databáze: | OpenAIRE |
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