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DC Field | Value | Language |
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dc.contributor | Lindsay, J. | en_US |
dc.contributor | Othman, J. | en_US |
dc.contributor | Kerridge, I. | en_US |
dc.contributor | Fay, K. | en_US |
dc.contributor | Stevenson, W. | en_US |
dc.contributor | Arthur, C. | en_US |
dc.contributor | Chen, S. | en_US |
dc.contributor | Kong, David C. M. | en_US |
dc.contributor | Pergam, S. | en_US |
dc.contributor | Liu, C. | en_US |
dc.contributor | Slavin, M. | en_US |
dc.contributor | Greenwood, M. | en_US |
dc.date.accessioned | 2021-10-04T00:40:18Z | - |
dc.date.available | 2021-10-04T00:40:18Z | - |
dc.date.issued | 2021 | - |
dc.identifier.govdoc | 01720 | en_US |
dc.identifier.uri | http://hdl.handle.net/11054/1766 | - |
dc.description.abstract | Abstract 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.provenance | Submitted by Gemma Siemensma (gemmas@bhs.org.au) on 2021-08-06T04:12:33Z No. of bitstreams: 0 | en |
dc.description.provenance | Approved for entry into archive by Gemma Siemensma (gemmas@bhs.org.au) on 2021-10-04T00:40:18Z (GMT) No. of bitstreams: 0 | en |
dc.description.provenance | Made available in DSpace on 2021-10-04T00:40:18Z (GMT). No. of bitstreams: 0 Previous issue date: 2021 | en |
dc.title | Cytomegalovirus (CMV) management in allogeneic hematopoietic cell transplantation: Pre-transplant predictors of survival, reactivation, and spontaneous clearance. | en_US |
dc.type | Journal Article | en_US |
dc.type.specified | Article | en_US |
dc.bibliographicCitation.title | Transplant Infectious Disease | en_US |
dc.bibliographicCitation.volume | 23 | en_US |
dc.bibliographicCitation.issue | 3 | en_US |
dc.bibliographicCitation.stpage | e13548 | en_US |
dc.subject.healththesaurus | CYTOMEGALOVIRUS | en_US |
dc.subject.healththesaurus | HEMATOPOIETIC CELL TRANSPLANTATION | en_US |
dc.subject.healththesaurus | PRE-EMPTIVE THERAPY | en_US |
dc.subject.healththesaurus | VIREMIA | en_US |
dc.identifier.doi | https://doi.org/10.1111/tid.13548 | en_US |
Appears in Collections: | Research Output |
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