Evidence map›Paper›PMID 42683106›Full record

ArticleOpen forum infectious diseases2026

Multi-Criteria Decision Analysis using Physician Preferences from a Global Discrete Choice Experiment to Investigate the Selection of Preemptive Antiviral Treatments for Post-Hematopoietic Cell Transplant Cytomegalovirus Infection.

Miguel-Angel Perales, Jo-Anne H Young, Tommi Tervonen, Stephane Deparis, Jonathan D Norton, Cristian Gugiu, Tien Bo, Kimberly Davis, ShunPing Quan, Victoria L Prince and 2 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Miguel-Angel PeralesAdult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.ORCID https://orcid.org/0000-0002-5910-4571
Jo-Anne H YoungDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, USA.ORCID https://orcid.org/0000-0003-4182-341X
Tommi TervonenKielo Research, Zug, Switzerland.
Stephane DeparisKielo Research, Zug, Switzerland.
Jonathan D NortonTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.ORCID https://orcid.org/0000-0001-6275-8747
Cristian GugiuTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Tien BoTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Kimberly DavisTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
ShunPing QuanTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Victoria L PrinceTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.ORCID https://orcid.org/0009-0008-4567-702X
Adel Abou AliTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.
Jessica AucielloTakeda Development Center Americas, Inc., Cambridge, Massachusetts, USA.ORCID https://orcid.org/0000-0001-8247-7889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: A discrete choice experiment (DCE) subsequently incorporated into a multi-criteria decision analysis (MCDA) was used to compare clinicians' trade-offs between the benefits and risks of preemptive anti-cytomegalovirus (CMV) treatments posthematopoietic cell transplant (HCT). Methods: In the DCE, physicians completed forced-choice tasks comparing hypothetical treatments. We used logit models to estimate preference weights, relative attribute importance (RAI) score, and minimum acceptable benefit. The MCDA combined DCE-derived weighted attributes with clinical performance data to compare maribavir versus valganciclovir (using data from the AURORA study) and maribavir versus valganciclovir, ganciclovir, and foscarnet (using data from multiple sources). Analyses were conducted for 2 cohorts defined by baseline absolute neutrophil count (ANC) <1500/mm Results: In the DCE, all 7 attributes significantly impacted physician (n = 377) treatment choices; the most important were administration route/monitoring (RAI score = 25.7%), nephrotoxicity risk (RAI score = 18.5%), grade 3-4 neutropenia risk (RAI score = 18.1%), and week 8 viremia clearance (RAI score = 16.0%). Neutropenia at CMV reactivation significantly reduced physicians' preference for treatments with a higher grade 3-4 neutropenia risk. In the MCDA, overall benefit-risk scores were higher for maribavir than valganciclovir in both ANC cohorts. Among the considered attributes, the largest positive contributor to the overall benefit-risk score was viremia clearance at week 8, and the largest negative contributor was grade 3-4 neutropenia risk. Maribavir had a higher overall benefit-risk score than ganciclovir and foscarnet in both ANC cohorts. Conclusions: Within this MCDA framework, maribavir was preferred over valganciclovir, ganciclovir, and foscarnet for preemptive treatment of CMV after HCT.

Indexed as

cytomegalovirusdiscrete choice experimenthematopoietic cell transplantmulti-criteria decision analysisphysician treatment preference

Identifiers

PMID42683106
PMCPMC13532088

What Socratic holds

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Registered trials

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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 Socratic graph.