Evidence map›Paper›PMID 41180004›Full record

ArticleOpen forum infectious diseases2025

Cytomegalovirus Viral Load Continues to Predict Poor Outcomes in Adults and Children Despite Improved Hematopoietic Cell Transplantation Success.

Alicja Sadowska-Klasa, Hu Xie, Danniel Zamora, Alpana Waghmare, Joshua A Hill, Elizabeth R Duke, Margaret L Green, Masumi Ueda Oshima, Brenda M Sandmaier, Keith R Jerome and 2 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Cytomegalovirus and Aging-How Can the Field Move Forward?The Journal of infectious diseases · 2026
    Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Alicja Sadowska-KlasaVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Hu XieClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-0556-6591
Danniel ZamoraVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-1318-2902
Alpana WaghmareVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-2268-9470
Joshua A HillVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-7665-7100
Elizabeth R DukeVeterans Affairs Palo Alto Health Care System, Palo Alto, California, USA.ORCID https://orcid.org/0000-0002-3348-9039
Margaret L GreenDivision of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-5591-0779
Masumi Ueda OshimaDivision of Hematology and Oncology, University of Washington, Seattle, WA,USA.ORCID https://orcid.org/0000-0003-2277-1976
Brenda M SandmaierDivision of Hematology and Oncology, University of Washington, Seattle, WA,USA.ORCID https://orcid.org/0000-0002-9767-9739
Keith R JeromeVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-8212-3789
Wendy M LeisenringClinical Research Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.ORCID https://orcid.org/0000-0001-7405-0906
Michael BoeckhVaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, Washington, USA.

Funding

Cytomegalovirus-specific Immune Reconstitution after Hematopoietic Cell Transplantation in the Era of Modern Antiviral ProphylaxisK23AI163343 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Danniel Zamora · 2022 to 2026
$945k
NIAID NIH HHS K23 AI163343
6 · The paper itself

Abstract

Background: Recent advances of graft-versus-host disease prevention strategies have led to improved overall survival after hematopoietic cell transplantation (HCT). Whether cytomegalovirus (CMV) viral load continues to predict CMV disease, overall mortality, and nonrelapse mortality is poorly defined. Methods: CMV-seropositive patients undergoing allogeneic HCT between 2007 and 2017 with weekly CMV DNA polymerase chain reaction surveillance and preemptive therapy were analyzed. Multivariate Cox proportional hazards models were used to estimate the association between CMV viral load by day 100 at different thresholds with CMV disease and overall and nonrelapse mortality up to 1 year post-HCT. Results: Of 1539 patients who received a transplant in the study period, 1349 survived >100 days after HCT and were included in the analyses. By day 100 post-HCT, CMV reactivation at any level was observed in 76%, with the lowest incidence at all levels in young children. Pediatric patients had significantly less CMV disease compared to the adult population. CMV reactivation was associated with a higher risk of CMV disease (adjusted hazard ratio, 6.8 [95% confidence interval, 3.54-13]); it was also associated with overall and nonrelapse mortality among day 100 survivors, although the association was diminished recently. The strongest correlation was still apparent between viral load and mortality in patients with a viral load >3 log Conclusions: CMV viral load continued to be a strong predictor for CMV disease. With improved transplantation techniques, the association of viral load with overall and nonrelapse mortality is diminished, but the effect was still present in patients with severe immunosuppression.

Indexed as

association with mortalityCMV diseaseCMV viral load

Identifiers

PMID41180004
PMCPMC12574539

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.