Evidence map›Paper›PMID 41915767›Full record

ArticleAntimicrobial agents and chemotherapy2026

Analysis of interactions between posaconazole/voriconazole and venetoclax.

Chunqing Liu, Xiaoyan Xie, Mei Sun, Pengzhou Hang, Jinxiu Lyu, Yibing Shi, Xiang Gao, Wenjun Xu, Hua Zhu

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2026. 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

9 authors.

Chunqing LiuSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, Nanjing, China.
Xiaoyan XieDepartment of Hematology, Northern Jiangsu People's Hospital, Yangzhou, China.
Mei SunDepartment of Hematology, Northern Jiangsu People's Hospital, Yangzhou, China.
Pengzhou HangFaculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.
Jinxiu LyuFaculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.
Yibing ShiFaculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.
Xiang GaoFaculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.
Wenjun Xu *Faculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.ORCID 0009-0004-8060-3131
Hua Zhu *Faculty of Pharmacy, Northern Jiangsu People's Hospital, Yangzhou, China.ORCID 0009-0009-1877-2467

Funding

Jiangsu Provincial Hospital Association-Hospital Management Innovation Research Project JSYGY-3-2024-667Jiangsu Provincial Medical Association-Aosikang Hospital Medical Science Foundation Project A202332
6 · The paper itself

Abstract

Venetoclax (VEN), a selective BCL-2 inhibitor predominantly metabolized by CYP3A4, is a cornerstone therapeutic for myeloid neoplasms (MNs). Patients with myeloid malignancies are at elevated risk of invasive fungal infections (IFIs), and triazole antifungal drugs, such as posaconazole (PCZ) and voriconazole (VCZ), are commonly used for prophylaxis or treatment. These agents are potent CYP3A4 inhibitors and will exhibit significant potential for pharmacokinetic drug-drug interactions with VEN. Although studies on their interaction are limited, such combinations are frequently used in clinical practice, making further research highly significant. This study aimed to investigate the changes in blood concentration and the safety of VEN when combined with triazole antifungal drugs (PCZ and VCZ). Patients with MN treated with VEN from April 2023 to April 2025 were enrolled and allocated to the VEN monotherapy group and the VEN plus triazole antifungal drug group. We collected baseline demographic characteristics and monitored adverse events. Steady-state plasma concentrations of VEN were quantified using the liquid chromatography-mass spectrometry methodology. Statistical analyses, including comparative assessments of plasma concentrations and adverse event rates, were performed using IBM SPSS Statistics 26. A total of 54 patients were enrolled in the study. Following VEN dose reduction to 100 mg, plasma concentrations in the VEN + PCZ/VCZ group remained significantly elevated compared to the VEN group (

Indexed as

Antifungal AgentsBridged Bicyclo Compounds, HeterocyclicSulfonamidesTriazolesVoriconazoleAgedDrug InteractionsFemaleHumansMaleMiddle AgedAntifungal AgentsBridged Bicyclo Compounds, HeterocyclicposaconazoleSulfonamidesTriazolesvenetoclaxVoriconazoleblood concentration monitoringinteractionmyeloid neoplasmsposaconazolevenetoclaxvoriconazole

Identifiers

PMID41915767
PMCPMC13148035

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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.