Evidence map›Paper›PMID 40082544›Full record

ArticleScientific reports2025

POD24-Based prognostic signature enables personalized risk stratification in mantle cell lymphoma.

Yizi He, Caiqin Wang, Tao Pan, Qingqing Cai, Dehui Zhou, Huilai Zhang, Rong Liang, Dongfeng Zeng, Haige Ye, Yun Liang and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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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

13 authors.

Yizi He *Department of Lymphoma & Hematology, the Affiliated Tumor Hospital of Xiangya Medical School, Central South University, Changsha, Hunan, China.
Caiqin Wang *Department of Lymphoma & Hematology, the Affiliated Tumor Hospital of Xiangya Medical School, Central South University, Changsha, Hunan, China.
Tao PanThe Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qingqing CaiDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, China.
Dehui ZhouInstitute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Huilai ZhangDepartment of Lymphoma, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Tianjin'S Clinical Research Center for Cancer, Tianjin, China.
Rong LiangDepartment of Hematology, Department of Internal Medicine, Xijing Hospital, Air Force Medical University, Xi'an, Shaanxi, China.
Dongfeng ZengDepartment of Hematology, Daping Hospital, Army Medical University, Third Military Medical University), Chongqing, China.
Haige YeDepartment of Hematology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Yun LiangDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Xiuhua SunDepartment of Oncology, The Second Hospital of Dalian Medical University, Dalian, Liaoning, China.
Ling XiaoDepartment of Histology and Embryology of School of Basic Medical Sciences, Central South University, Changsha, Hunan, China. xiaolingcsu@csu.edu.cn.
Hui ZhouDepartment of Lymphoma & Hematology, the Affiliated Tumor Hospital of Xiangya Medical School, Central South University, Changsha, Hunan, China. zhouhui9403@126.com.

Funding

Health Commission of Hunan Province 202203045455Hunan Provincial Clinical Medical Research Center for Lymphatic tumor 2021SK4015National Outstanding Youth Science Fund Project of National Natural Science Foundation of China 82000200Xisike-Xinda Clinical Oncology Research Foundation Y-XD202002-0104
6 · The paper itself

Abstract

Mantle cell lymphoma (MCL) exhibits significant biological and clinical heterogeneity, necessitating a refined prognostic model. According to the drawbacks of existing models which do not truly define the complexity of the disease, we used the clinical and molecular data from nine medical centers of China to validate the predictive utility of progression of disease within 24 months (POD24), and also established a novel prognostic risk model to predict the survival outcome of MCL patients. POD24 occurred in 37.7% of evaluable patients, with the median over survival being 21 months (vs. 122 months for those without POD24, P < 0.0001). The POD24-based risk model had the highest sensitivity to predict survival with the most satisfying AUC value for risk score (AUC = 0.869). In conclusion, we confirm the obviously predictive performance of POD24 and established a novel risk model combined POD24 and clinical factors. Our new prognostic model might be helpful in effectively classify MCL patients with high-risk groups in terms of survival rate, which may help in selecting high-risk MCL patients for more intensive treatment at time of relapse.

Indexed as

Biomarkers, TumorLymphoma, Mantle-CellAdultAgedChinaDisease ProgressionFemaleHumansMaleMiddle AgedPrecision MedicinePrognosisRisk AssessmentBiomarkers, TumorClinical factorMantle cell lymphomaPrognosticProgression of disease within 24 months

Identifiers

PMID40082544
PMCPMC11906600

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