Laboratory Prognostic Index (LAB-PI) in diffuse large B-cell lymphoma: a single blood analysis predicts outcomes as good as IPI, NCCN-IPI, and GELTAMO-IPI.
1/5 보강
[BACKGROUND] Many prognostic variables have been described in diffuse large B-cell lymphoma (DLBCL) and combined in prognostic scores, which are not usually fully objective and may be complex to apply
- 표본수 (n) 221
APA
Martin-Moro F, Bento L, et al. (2025). Laboratory Prognostic Index (LAB-PI) in diffuse large B-cell lymphoma: a single blood analysis predicts outcomes as good as IPI, NCCN-IPI, and GELTAMO-IPI.. ESMO open, 10(12), 105873. https://doi.org/10.1016/j.esmoop.2025.105873
MLA
Martin-Moro F, et al.. "Laboratory Prognostic Index (LAB-PI) in diffuse large B-cell lymphoma: a single blood analysis predicts outcomes as good as IPI, NCCN-IPI, and GELTAMO-IPI.." ESMO open, vol. 10, no. 12, 2025, pp. 105873.
PMID
41297160 ↗
Abstract 한글 요약
[BACKGROUND] Many prognostic variables have been described in diffuse large B-cell lymphoma (DLBCL) and combined in prognostic scores, which are not usually fully objective and may be complex to apply. With the aim of designing and validating a simple, inexpensive, objective, and reproducible prognostic tool in DLBCL, the Laboratory Prognostic Index (LAB-PI) was developed.
[PATIENTS AND METHODS] Laboratory parameters routinely evaluated at DLBCL diagnosis were analysed before treatment initiation in a DLBCL cohort (n = 221). The variables associated with event-free survival (EFS) were combined into the new score and graded according to their prognostic impact in multivariate analysis. Patients were clustered according to their risk. The LAB-PI was validated in an independent cohort (n = 885) and compared with other DLBCL scores.
[RESULTS] The LAB-PI included three laboratory variables routinely assessed at DLBCL diagnosis: elevated lactate dehydrogenase (LDH) (1 point), anaemia (1 point), and high β2-microglobulin (B2M) up to two times the upper limit of normal (ULN) (1 point) or greater than two times the ULN (2 points). Cases were clustered into four groups according to their prognosis in the validation cohort: low risk (0 points, 5-year EFS 87%), low-intermediate risk (1-2 points, 5-year EFS 69%), high-intermediate risk (3 points, 5-year EFS 55%), and high risk (4 points, 5-year EFS 37%). The LAB-PI was comparable with the International Prognostic Index (IPI), National Cancer Comprehensive Network (NCCN)-IPI, and Grupo Español de Linfomas/Trasplante de Médula ósea (GELTAMO)-IPI in predicting prognosis and remained useful in subanalysis according to age and stage.
[CONCLUSION] The LAB-PI predicts outcome in newly diagnosed DLBCL patients by a single blood assessment including LDH, haemoglobin, and B2M.
[PATIENTS AND METHODS] Laboratory parameters routinely evaluated at DLBCL diagnosis were analysed before treatment initiation in a DLBCL cohort (n = 221). The variables associated with event-free survival (EFS) were combined into the new score and graded according to their prognostic impact in multivariate analysis. Patients were clustered according to their risk. The LAB-PI was validated in an independent cohort (n = 885) and compared with other DLBCL scores.
[RESULTS] The LAB-PI included three laboratory variables routinely assessed at DLBCL diagnosis: elevated lactate dehydrogenase (LDH) (1 point), anaemia (1 point), and high β2-microglobulin (B2M) up to two times the upper limit of normal (ULN) (1 point) or greater than two times the ULN (2 points). Cases were clustered into four groups according to their prognosis in the validation cohort: low risk (0 points, 5-year EFS 87%), low-intermediate risk (1-2 points, 5-year EFS 69%), high-intermediate risk (3 points, 5-year EFS 55%), and high risk (4 points, 5-year EFS 37%). The LAB-PI was comparable with the International Prognostic Index (IPI), National Cancer Comprehensive Network (NCCN)-IPI, and Grupo Español de Linfomas/Trasplante de Médula ósea (GELTAMO)-IPI in predicting prognosis and remained useful in subanalysis according to age and stage.
[CONCLUSION] The LAB-PI predicts outcome in newly diagnosed DLBCL patients by a single blood assessment including LDH, haemoglobin, and B2M.