Evidence map›Paper›PMID 41814909›Full record

ArticleSe pu = Chinese journal of chromatography2026

[Rapid determination of venetoclax in plasma by ultra performance liquid chromatography-tandem mass spectrometry].

Ying Zhu, Xiao-Li Ma, Song-Lin Yu, Ling Qiu

Abstract readEnglish Abstract
In one paragraph

Article in Se pu = Chinese journal of chromatography, 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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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

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3 · Its place in the literature

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4 · The record

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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

4 authors.

Ying ZhuDepartment of Laboratory Medicine,Peking Union Medical College Hospital,Peking Union Medical College & Chinese Academy of Medical Science,Beijing 100730,China.
Xiao-Li MaDepartment of Laboratory Medicine,Peking Union Medical College Hospital,Peking Union Medical College & Chinese Academy of Medical Science,Beijing 100730,China.
Song-Lin YuDepartment of Laboratory Medicine,Peking Union Medical College Hospital,Peking Union Medical College & Chinese Academy of Medical Science,Beijing 100730,China.
Ling QiuDepartment of Laboratory Medicine,Peking Union Medical College Hospital,Peking Union Medical College & Chinese Academy of Medical Science,Beijing 100730,China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukemia is a malignant tumor of the hematological system characterized by the uncontrolled proliferation of abnormal hematopoietic cells in the bone marrow. It often presents with anemia, bleeding tendency, infection risk and organ invasion. These clinical symptoms bring severe survival risks to patients. Although traditional chemotherapy regimens are effective in the treatment of some hematological malignancies, their efficacy is limited for elderly patients, those with high-risk genetic characteristics or comorbidities. In recent years, targeted drugs have revolutionized the treatment of leukemia. By selectively inducing tumor cell apoptosis, they have significantly improved the remission rate and survival prognosis of patients with multiple leukemia subtypes. Venetoclax is a B-cell lymphoma 2 (BCL-2) inhibitor and plays an important role in the clinical treatment of hematological malignancies, such as acute myeloid leukemia and chronic lymphocytic leukemia. In addition, it also shows potential efficacy in other hematological malignancies such as multiple myeloma and mantle cell lymphoma. Although the efficacy of venetoclax is remarkable, the individual differences in blood drug concentration are significant due to factors such as drug interactions, polymorphisms of metabolic enzymes, and liver and kidney function. Venetoclax exhibits significant inter-individual pharmacokinetic differences, the trough concentration is significantly correlated with the treatment response, and if the peak concentration exceeds the warning concentration, adverse reactions will be triggered. Clinical trials have reported a variety of adverse events associated with venetoclax, including neutropenia, tumor lysis syndrome, thrombocytopenia, infection, anemia, diarrhea, nausea, upper respiratory tract infection, cough and musculoskeletal pain. Therefore, to minimize the risk of adverse events in the clinical use of venetoclax as much as possible, it is necessary to reasonably guide its clinical dosage. Therapeutic drug monitoring can optimize individual dosing regimens by measuring the steady-state concentration in patients' blood. This research aims to establish a rapid, sensitive and reliable ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method. This method is used for the quantitative determination of venetoclax in plasma, and its performance was validated. This method employs an electrospray ionization and multiple reaction monitoring (MRM) in the positive ion mode to detect venetoclax and its isotope internal standard venetoclax-d

Indexed as

Antineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicSulfonamidesTandem Mass SpectrometryChromatography, High Pressure LiquidHumansLeukemiaAntineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclaxplasmatherapeutic drug monitoringultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)venetoclax

Identifiers

PMID41814909
PMCPMC12980510

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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.