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Early prediction of adult lymphoma-associated haemophagocytic lymphohistiocytosis using an interpretable machine learning model.

1/5 보강
British journal of haematology 2026
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PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
126 patients diagnosed with LA-HLH and 254 with non-LA-HLH.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Finally, the optimal model was deployed as a web-based tool to support early aetiological differentiation. This may facilitate prompt initiation of targeted examination and appropriate treatment for patients with LA-HLH.

Luan M, Jia R, Wang D, Zhang F, Han X, Sheng X, Li S, Zhou Q, Li B, Ning C, Ji C, Ye J, Zang S, Lu F

📝 환자 설명용 한 줄

Lymphoma-associated haemophagocytic lymphohistiocytosis (LA-HLH) is associated with a high mortality rate, making early diagnosis and appropriate treatment critical for improving patient outcomes.

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BibTeX ↓ RIS ↓
APA Luan M, Jia R, et al. (2026). Early prediction of adult lymphoma-associated haemophagocytic lymphohistiocytosis using an interpretable machine learning model.. British journal of haematology. https://doi.org/10.1111/bjh.70447
MLA Luan M, et al.. "Early prediction of adult lymphoma-associated haemophagocytic lymphohistiocytosis using an interpretable machine learning model.." British journal of haematology, 2026.
PMID 41871894
DOI 10.1111/bjh.70447

Abstract

Lymphoma-associated haemophagocytic lymphohistiocytosis (LA-HLH) is associated with a high mortality rate, making early diagnosis and appropriate treatment critical for improving patient outcomes. In this study, we enrolled 126 patients diagnosed with LA-HLH and 254 with non-LA-HLH. A machine learning-based predictive model was developed and validated to enable timely differentiation of LA-HLH from other HLH subtypes. The model incorporated 11 predictive variables for early LA-HLH prediction, among which the top five most influential were age, ferritin, monocyte percentage, haemoglobin and platelet count. Among seven machine learning algorithms evaluated, the random forest model demonstrated the best performance, achieving an area under the curve (AUC) of 0.946 on the training set and 0.794 on the validation set. We subsequently evaluated combined models that incorporated disease-specific indicators such as soluble interleukin-2 receptor (sCD25) and PET-CT SUVmax, which resulted in a non-significant increase in AUC on the validation set. Finally, the optimal model was deployed as a web-based tool to support early aetiological differentiation. This may facilitate prompt initiation of targeted examination and appropriate treatment for patients with LA-HLH.

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