Evidence map›Paper›PMID 41586228›Full record

ArticleFrontiers in nutrition2025

Simple biomarkers based on CRP and albumin predict clinical outcomes in adult patients with T-cell acute lymphoblastic leukaemia.

Aiwen Li, Jun Wen, Xianfang Shao, Qiuju Liu

Abstract read
In one paragraph

Article in Frontiers in nutrition, 2025. 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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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

4 authors.

Aiwen LiDepartment of Haematology, Cancer Center, The First Hospital of Jilin University, Changchun, China.
Jun WenDepartment of Haematology, Cancer Center, The First Hospital of Jilin University, Changchun, China.
Xianfang ShaoDepartment of Intensive Care Medicine, Zibo Central Hospital, Zibo, China.
Qiuju LiuDepartment of Haematology, Cancer Center, The First Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Inflammation and malnutrition adversely impact outcomes in patients with various malignancies. Composite indices such as the C-reactive protein/albumin ratio (CAR), the CRP × fibrinogen/albumin ratio (CFA), and the modified Glasgow Prognostic Score (mGPS) integrate these parameters, although their prognostic role in T-cell acute lymphoblastic leukaemia (T-ALL) remains underexplored. Methods: In this single-centre retrospective study, 74 adults with T-ALL were included. CAR, CFA, and mGPS were calculated at diagnosis. Receiver operating characteristic curve analysis revealed the optimal cut-off values for the CAR (0.387) and CFA (0.396). Patients were stratified into low- and high-risk groups. Endpoints included rates of complete remission/complete remission with incomplete haematologic recovery (CR/CRi) at end-of-induction (EOI), minimal residual disease (MRD), overall survival (OS), and progression-free survival (PFS). Results: Patients with low CAR, low CFA, or mGPS0 achieved significantly higher rates of CR/CRi (all Conclusion: Pretreatment CAR, CFA, and mGPS are robust, accessible prognostic biomarkers in adults with T-ALL. Their integration into initial risk assessment could help guide personalized treatment strategies, including the identification of high-risk patients who may derive greater benefit from aggressive interventions.

Indexed as

acute lymphocytic leukaemiaalbuminC-reactive proteinfibrinogenprognosis

Identifiers

PMID41586228
PMCPMC12823328

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