Please use this identifier to cite or link to this item: http://hdl.handle.net/11054/1766
Full metadata record
DC FieldValueLanguage
dc.contributorLindsay, J.en_US
dc.contributorOthman, J.en_US
dc.contributorKerridge, I.en_US
dc.contributorFay, K.en_US
dc.contributorStevenson, W.en_US
dc.contributorArthur, C.en_US
dc.contributorChen, S.en_US
dc.contributorKong, David C. M.en_US
dc.contributorPergam, S.en_US
dc.contributorLiu, C.en_US
dc.contributorSlavin, M.en_US
dc.contributorGreenwood, M.en_US
dc.date.accessioned2021-10-04T00:40:18Z-
dc.date.available2021-10-04T00:40:18Z-
dc.date.issued2021-
dc.identifier.govdoc01720en_US
dc.identifier.urihttp://hdl.handle.net/11054/1766-
dc.description.abstractAbstract Background: Cytomegalovirus (CMV) reactivation is a frequent complication after allogeneic hematopoietic cell transplant (alloHCT). Method: We analyzed 159 alloHCT recipients with 4409 quantitative CMV viral loads to determine pre-transplant predictors of CMV reactivation, clinically significant CMV infection (cs-CMVi, defined as CMV viral load >1000 IU/mL), CMV disease, kinetics of spontaneous clearance of CMV, and survival using a standardized pre-emptive therapy approach to identify at-risk groups to target prevention strategies. Results: Cs-CMVi was most common in D-/R+ unrelated donor transplants (URD). Spontaneous CMV clearance occurred in 26% of patients who reached a viral load of 56-137 IU/mL, 6% at 138-250 IU/mL and in one patient >250 IU/mL. Median time between the first CMV reactivation (>56 IU/mL) and a viral load >250 IU/mL was 13 days, whereas the time from the first viral load >250 IU/mL to reach a vial load >1000 IU/mL was 4 days. Cs-CMVi was associated with a significant increase in non-relapse mortality (NRM) on multivariate analysis. Conclusions: Overall, this study indicates that D-/R+ URD recipients are at high-risk for cs-CMVi- and CMV-related mortality, and are potential candidates for targeted CMV prophylaxis. Spontaneous clearance of CMV beyond a viral load of 250 IU/mL is uncommon, suggesting that this could be used as an appropriate threshold to initiate pre-emptive therapy.en_US
dc.description.provenanceSubmitted by Gemma Siemensma (gemmas@bhs.org.au) on 2021-08-06T04:12:33Z No. of bitstreams: 0en
dc.description.provenanceApproved for entry into archive by Gemma Siemensma (gemmas@bhs.org.au) on 2021-10-04T00:40:18Z (GMT) No. of bitstreams: 0en
dc.description.provenanceMade available in DSpace on 2021-10-04T00:40:18Z (GMT). No. of bitstreams: 0 Previous issue date: 2021en
dc.titleCytomegalovirus (CMV) management in allogeneic hematopoietic cell transplantation: Pre-transplant predictors of survival, reactivation, and spontaneous clearance.en_US
dc.typeJournal Articleen_US
dc.type.specifiedArticleen_US
dc.bibliographicCitation.titleTransplant Infectious Diseaseen_US
dc.bibliographicCitation.volume23en_US
dc.bibliographicCitation.issue3en_US
dc.bibliographicCitation.stpagee13548en_US
dc.subject.healththesaurusCYTOMEGALOVIRUSen_US
dc.subject.healththesaurusHEMATOPOIETIC CELL TRANSPLANTATIONen_US
dc.subject.healththesaurusPRE-EMPTIVE THERAPYen_US
dc.subject.healththesaurusVIREMIAen_US
dc.identifier.doihttps://doi.org/10.1111/tid.13548en_US
Appears in Collections:Research Output

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.