Evidence map›Paper›PMID 39444262›Full record

ArticleCancer medicine2024

Development and validation of a hierarchical approach for lymphoma classification using immunohistochemical markers.

Jiming Xu, Yunfei Shi, Mengxuan Cui, Yao Wang, Wenhui Fan, Jingping Yun, Linfeng Li, Muyan Cai

Abstract readValidation Study
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jiming XuDepartment of Automation, Tsinghua University, Beijing, China.
Yunfei ShiKey Laboratory of Carcinogenesis and Translational Research, Department of Pathology, Ministry of Education, Peking University Cancer Hospital and Institute, Beijing, China.
Mengxuan CuiYidu Cloud Technology Inc, Beijing, China.ORCID https://orcid.org/0000-0002-6471-8164
Yao WangYidu Cloud Technology Inc, Beijing, China.
Wenhui FanDepartment of Automation, Tsinghua University, Beijing, China.
Jingping YunCollaborative Innovation Center for Cancer Medicine, State Key Laboratory of Oncology in South China, Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Linfeng LiYidu Cloud Technology Inc, Beijing, China.
Muyan CaiCollaborative Innovation Center for Cancer Medicine, State Key Laboratory of Oncology in South China, Department of Pathology, Sun Yat-sen University Cancer Center, Guangzhou, China.

Funding

Hebei Provincial Health and Family Planning Commission Scientific Research Fund Project 20211021National Key Research and Development Program of China 2022YFC2009805
6 · The paper itself

Abstract

backgroundAccurate lymphoma classification is critical for effective treatment and immunohistochemistry is a cost-effective and time-saving approach. Although several machine learning algorithms showed effective results, they focused on a specific task of classification but not the whole classification workflow, thus impractical to be applied in clinical settings. Thus, we aim to develop an effective and economic machine learning-assisted system that can streamline the lymphoma differential diagnostic workflow using EBER in situ hybridization and immunohistochemical markers.

methodsWe included pathological reports diagnosed as lymphomas from two cancer centers (Sun Yat-sen University Cancer Center and Peking University Cancer Hospital & Institute). We proposed a hierarchical approach that mimicked the human diagnostic process and employed simplified panels of markers to perform a series of interpretable classification. The diagnostic accuracy for lymphoma pathological subtypes and the markers saving ratio were investigated in both temporal independent population and external medical center.

resultsA total of 14,927 patients and corresponding immunohistochemical results from two cancer centers were included. The proposed system had high discriminative ability for differentiating lymphoma pathological subtypes (measured by mean AUC in three validation cohorts, non-Hodgkin and Hodgkin lymphoma: 0.959; non-Hodgkin subtypes: 0.983; B-lymphoma subtypes: 0.868; T-lymphoma subtypes: 0.962; DLBCL subtypes: 0.957). In addition, the system's well selected characteristics can contribute to the development of agreement on panels of markers for differential diagnosis and help minimize cost of immunohistochemical marker techniques (measured by marker saving ratio compared to real clinical settings, internal primary-stage cohort: 16.45% saved, p < 0.001; internal later-stage cohort: 21.73% saved, p < 0.001; external cohort: 3.67% saved, p < 0.001).

conclusionsMachine learning-based hierarchical system using EBER in situ hybridization and IHC markers was developed, which could streamline the workflow by sequentially determining each lymphoma pathological subtype. The proposed system proved to be effective and cost-saving in independent and external validation, thus could be adopted affordably in future clinical practice.

Indexed as

Biomarkers, TumorImmunohistochemistryLymphomaMachine LearningAdolescentAdultAgedDiagnosis, DifferentialFemaleHumansLymphoma, Non-HodgkinMaleMiddle AgedYoung AdultBiomarkers, Tumordiagnosisimmunohistochemistrylymphomasmachine learning

Identifiers

PMID39444262
PMCPMC11499568

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