Evidence map›Paper›PMID 38924728›Full record

ArticleBlood advances2024

CMV reactivation during pretransplantation evaluation: a novel risk factor for posttransplantation CMV reactivation.

Danniel Zamora, Hu Xie, Alicja Sadowska-Klasa, Eleftheria Kampouri, Melinda A Biernacki, Masumi Ueda Oshima, Elizabeth Duke, Margaret L Green, Louise E Kimball, Leona Holmberg and 7 more

Abstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Current and Future Strategies for the Prevention and Treatment of Cytomegalovirus Infections in Transplantation.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Review
  8. Article
  9. Review
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

17 authors.

Danniel ZamoraVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-1318-2902
Hu XieClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Alicja Sadowska-KlasaVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
Eleftheria KampouriVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0001-8019-3073
Melinda A BiernackiTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA.
Masumi Ueda OshimaClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-2277-1976
Elizabeth DukeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-3348-9039
Margaret L GreenDivision of Allergy & Infectious Disease, University of Washington School of Medicine, Seattle, WA.ORCID 0000-0002-5591-0779
Louise E KimballVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
Leona HolmbergClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.
Alpana WaghmareDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA.
Alexander L GreningerVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
Keith R JeromeVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0002-8212-3789
Geoffrey R HillTranslational Science and Therapeutics Division, Fred Hutchinson Cancer Center, Seattle, WA.
Joshua A HillVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-0942-9834
Wendy M LeisenringClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0001-7405-0906
Michael J BoeckhVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Training Program in Infectious Diseases in the Immunocompromised HostT32AI118690 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BOECKH, MICHAEL J · 2016 to 2025
$4.0M
Defining Protective CMV Immunity after TransplantationR01AI175535 · NIAID · FRED HUTCHINSON CANCER CENTER · PI Geoffrey Roger HILL · 2023 to 2026
$3.0M
Infections in Hematopoietic Cell Transplant RecipientsK24HL093294 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI BOECKH, MICHAEL J · 2009 to 2019
$1.5M
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
CMV Entry-Specific Neutralizing Antibody in Primary Infection in TransplantationK23AI097234 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GREEN, MARGARET L · 2012 to 2016
$653k
NCI NIH HHS P30 CA015704NHLBI NIH HHS K24 HL093294NIAID NIH HHS K23 AI097234NIAID NIH HHS K23 AI163343NIAID NIH HHS R01 AI175535NIAID NIH HHS T32 AI118690
6 · The paper itself

Abstract

abstractCytomegalovirus (CMV) disease occurs occasionally before allogeneic hematopoietic cell transplantation (HCT) and is associated with poor post-HCT outcomes; however, the impact of pre-HCT CMV reactivation is unknown. Pre-HCT CMV reactivation was assessed in HCT candidates from the preemptive antiviral therapy (2007-2017) and letermovir prophylaxis (2018-2021) eras. CMV DNA polymerase chain reaction (PCR) surveillance was routinely performed during the pre-HCT workup period, and antiviral therapy was recommended according to risk of progression to CMV disease. Risk factors for pre-HCT CMV reactivation were characterized, and the associations of pre-HCT CMV reactivation with post-HCT outcomes were examined using logistic regression and Cox proportional hazard models, respectively. A total of 1694 patients were identified, and 11% had pre-HCT CMV reactivation 14 days (median; interquartile range [IQR], 6-23) before HCT. Lymphopenia (≤0.3 × 103/μL) was the strongest risk factor for pre-HCT CMV reactivation at multiple PCR levels. In the preemptive therapy era, patients with pre-HCT CMV reactivation had a significantly increased risk of CMV reactivation by day 100 as well as CMV disease and death by 1 year after HCT. Clearance of pre-HCT CMV reactivation was associated with a lower risk of post-HCT CMV reactivation. Similar associations with post-HCT CMV end points were observed in a cohort of patients receiving letermovir prophylaxis. Pre-HCT CMV reactivation can be routinely detected in high-risk HCT candidates and is a significant risk factor for post-HCT CMV reactivation and disease. Pre-HCT CMV DNA PCR surveillance is recommended in high-risk HCT candidates, and antiviral therapy may be indicated to prevent post-HCT CMV reactivation.

Indexed as

CytomegalovirusCytomegalovirus InfectionsHematopoietic Stem Cell TransplantationVirus ActivationAdultAgedAntiviral AgentsFemaleHumansMaleMiddle AgedRisk FactorsAntiviral Agents

Identifiers

PMID38924728
PMCPMC11399585

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.