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Record W4391598130 · doi:10.1016/j.jtct.2023.12.620

Impact of Letermovir on Outcomes in Cytomegalovirus Seropositive Patients Undergoing Allogeneic HCT: Exploring Outcomes across Ethnicities

2024· article· en· W4391598130 on OpenAlexaff
Sanjay Singhabahu, Elizabeth Herrity, Mats Remberger, Ian Pang, Igor Novitzky‐Basso, Ivan Pašić, Wilson Lam, Arjun Law, Auro Viswabandya, Armin Gerbitz, Rajat Kumar, Dennis Dong Hwan Kim, Jeffrey H. Lipton, Jonas Mattsson, Fotios V. Michelis

Bibliographic record

VenueTransplantation and Cellular Therapy · 2024
Typearticle
Languageen
FieldMedicine
TopicCytomegalovirus and herpesvirus research
Canadian institutionsUniversity Health NetworkPrincess Margaret Cancer Centre
Fundersnot available
KeywordsSerostatusMedicineClinical endpointCumulative incidenceInternal medicinePopulationIncidence (geometry)CohortCytomegalovirusRetrospective cohort studyImmunologyOncologyViral loadClinical trialHerpesviridaeViral diseaseVirus

Abstract

fetched live from OpenAlex

Cytomegalovirus (CMV) serostatus remains an independent adverse risk factor for increased transplant related morbidity and mortality (TRM) in CMV seropositive (CMV+) recipients versus CMV seronegative recipients1,2. Letermovir (LET) is a novel anti-CMV agent that prevents CMV replication through inhibition of the viral terminase complex3 and is routinely given as primary prophylaxis for CMV seropositive transplant recipients as it results in a lower risk of clinically significant CMV infections4. At our institution we serve a diverse ethnic population and utilize a heterogenous mixture of donor sources and graft-versus-host-disease (GVHD) prophylaxis. We conducted this study to evaluate the impact of LET in our diverse population to evaluate for LET impact on major outcomes and evaluate for efficacy variations by ethnicity. A retrospective study found that 556 CMV+ patients received HCT between 2018 and 2022 at the Princess Margaret Cancer Centre (PMCC), 219 of which received LET prophylaxis. Primary endpoint was comparing those receiving LET and not receiving LET prophylaxis (non-LET) in Overall Survival (OS), Non-Relapse Mortality (NRM), Cumulative Incidence of Relapse (CIR), and GVHD-Free | Relapse-Free Survival (GRFS). Secondary endpoints explored LET impact on Cumulative Incidence of CMV Reactivation (CI-CMV) and OS stratified by self-reported ethnicity. In comparing, OS, CIR, GRFS and NRM for all patients, LET and non-LET, no significant difference in outcomes was observed. Figure 1. A significant LET effect was observed on the CI-CMV for the entire cohort. The most profound LET effect was in the East Asian cohort (LET 22%, non-LET 80%, p<0.001). Figure 2. The South Asian cohort activated CMV most frequently while on LET (38.9%, CI 16.8-60.7). Figure 3. The CI-CMV was significant between cohorts, with LET cohort having fewer reactivations (23.2% vs 32.1% experiencing 1, 5.0% vs 14.3% experiencing 2, and 5.0% vs 21.4% experiencing 3 reactivations; p<0.001). In multivariate analysis, LET reduced CMV reactivations by 53% compared to non-LET (HR=0.47 | CI 0.39-0.55, p<0.001). Our results indicate no observable LET drug effect on OS, CIR, GRFS, and NRM. Our East Asian cohort experienced a significant decrease in CMV reactivation with LET. Our South Asian cohort reactivated CMV more often while on LET compared to other ethnic cohorts. Further research is warranted in extending LET duration in higher risk ethnicities and/or investigating other strategies to decrease CMV reactivation in cohorts experiencing less LET benefit.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.004
Threshold uncertainty score0.008

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0000.001
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0000.001
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.063
GPT teacher head0.362
Teacher spread0.299 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2024
Admission routes1
Has abstractno

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