Evidence map›Paper›PMID 42286861›Full record

ArticleThe Journal of international medical research2026

Cytomegalovirus prophylaxis using low-dose and ultra-low-dose valganciclovir for patients who have undergone allogeneic hematopoietic stem cell transplantation: A retrospective study.

Wei-Hsiang Tseng, Cheng-Hsien Lin, Yu-Chen Su, Ling-Chiao Teng, Chieh-Lin Jerry Teng

Abstract read
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Article in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Wei-Hsiang TsengDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taiwan.
Cheng-Hsien LinDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taiwan.
Yu-Chen SuDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taiwan.
Ling-Chiao TengDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taiwan.
Chieh-Lin Jerry TengDivision of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taiwan.ORCID 0000-0001-9744-0368

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveCytomegalovirus reactivation is a clinically significant complication after allogeneic hematopoietic stem cell transplantation. Valganciclovir is commonly used for cytomegalovirus prophylaxis; however, the optimal dosing strategy remains unclear. This study compared the efficacy and safety of ultra-low-dose valganciclovir (450 mg every other day) and low-dose valganciclovir (450 mg daily) in preventing cytomegalovirus reactivation after allogeneic hematopoietic stem cell transplantation.MethodsWe retrospectively reviewed adult patients who underwent allogeneic hematopoietic stem cell transplantation from January 2020 to December 2023. Individuals receiving low-dose (n = 31) or ultra-low-dose (n = 35) valganciclovir as cytomegalovirus prophylaxis were included. Cytomegalovirus DNAemia was evaluated within the first 14 weeks and then at 14-28 weeks after transplantation. Cytomegalovirus disease, acute graft-versus-host disease, survival outcomes, and hematologic toxicities were also assessed.ResultsThe prevalence of early cytomegalovirus reactivation was 13.8% in the low-dose group and 20.0% in the ultra-low-dose group (

Indexed as

Antiviral AgentsCytomegalovirusCytomegalovirus InfectionsHematopoietic Stem Cell TransplantationValganciclovirAdultDose-Response Relationship, DrugFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective StudiesTransplantation, HomologousVirus ActivationAntiviral AgentsValganciclovirCytomegalovirusdosehematopoietic stem cell transplantationvalganciclovir

Identifiers

PMID42286861
PMCPMC13263491

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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 OpenQuestion graph.