Evidence map›Paper›PMID 40626717›Full record

Observational studyMicrobiology spectrum2025

Efficacy and toxicity analysis of ganciclovir in patients with cytomegalovirus lung infection: what is new for target range of therapeutic drug monitoring.

Dongjie Guo, Xiaoxing Wang, Pengmei Li, Yongguang Shang, Lei Zhang, Yue Chen, Xudong Kong, Wenqian Chen

Abstract readObservational Study
In one paragraph

Observational study in Microbiology spectrum, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Dongjie GuoDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.ORCID 0009-0008-8030-3111
Xiaoxing WangDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.
Pengmei LiDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.
Yongguang ShangDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.
Lei ZhangDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.
Yue ChenDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.ORCID 0000-0002-3907-7641
Xudong KongDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.
Wenqian ChenDepartment of pharmacy, China-Japan Friendship Hospital, Beijing, China.ORCID 0000-0003-1546-6930

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To investigate the relationship between ganciclovir trough concentration and its clinical efficacy and safety in patients with pulmonary cytomegalovirus (CMV) infection and to evaluate the target value of therapeutic drug monitoring (TDM) for predicting clinical efficacy or toxicity, an observational study was conducted on patients with CMV lung infection between Jan. 2021 and Dec. 2023. Target trough ganciclovir concentrations were collected during TDM, and clinical outcomes and adverse events (AEs) were assessed. Multiple regression analyses or binary logistic regression were used to analyze the factors affecting ganciclovir trough concentrations and clinical efficacy. The receiver operating characteristic (ROC) curve analysis identified ganciclovir trough concentration cutoffs as predictors of toxicity. Of 149 included patients, only 19.22% of trough concentrations reached the target range of 2-4 μg/mL. Diabetes, organ transplantation, and elevated hemoglobin levels decrease trough concentrations, whereas elevated blood creatinine and continuous renal replacement therapy (CRRT) increase trough concentrations. No relationship was found between the trough concentrations and the clinical outcomes. Organ transplantation, duration of ganciclovir administration, and albumin levels affect clinical efficacy. The ROC analysis identified ganciclovir trough concentrations of 0.985 (AUC = 0.600) and 0.995 µg/mL (AUC = 0.701) to be associated with decreased hemoglobin and elevated blood creatinine levels, respectively. No association was observed between ganciclovir trough concentration and clinical efficacy. However, thresholds for ganciclovir trough concentrations causing decreased hemoglobin and increased blood creatinine levels were identified. Renal replacement therapy is more likely to lead to elevated trough concentrations of ganciclovir. These findings suggest the importance of TDM for ganciclovir, and a new target range should be considered.IMPORTANCEAn observational study investigated the relationship between ganciclovir trough concentrations and clinical efficacy and safety. Only 19.22% of ganciclovir trough concentrations reached the target range of 2.0-4.0 μg/mL. Diabetes, organ transplantation, and elevated hemoglobin decreased trough concentrations, while elevated creatinine and CRRT increased concentrations. No relationship was found between ganciclovir trough concentrations and clinical outcomes in CMV lung infection. Organ transplantation, duration of ganciclovir administration, and albumin levels affected the clinical efficacy of ganciclovir. Critical ganciclovir trough concentrations of 0.985 and 0.995 μg/mL were associated with toxicity. The findings suggest the importance of therapeutic drug monitoring (TDM) with ganciclovir treatment.

Indexed as

Antiviral AgentsCytomegalovirus InfectionsDrug MonitoringGanciclovirAdultAgedCytomegalovirusFemaleHumansMaleMiddle AgedROC CurveTreatment OutcomeAntiviral AgentsGanciclovirclinical efficacycytomegalovirusganciclovirlung infectiontherapeutic drug monitoringtoxicitytrough concentration

Identifiers

PMID40626717
PMCPMC12323660

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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 OpenQuestion graph.