Key result
A novel immune-related prognostic index incorporating clinical factors and T-cell counts (CD4+ <26.7% and CD8+ >44.2%) showed better discrimination for overall survival than MIPI and MIPI-c.
Why the study?
The commonly used MIPI and combined MIPI risk classification indexes for mantle cell lymphoma lack immune-related parameters.
Does a novel immune-related prognostic index (IRPI) improve prediction of overall survival compared to MIPI and MIPI-c in patients with newly diagnosed mantle cell lymphoma?
Observational (n=339)
Yes
Does a novel immune-related prognostic index (IRPI) improve prediction of overall survival compared to MIPI and MIPI-c in patients with newly diagnosed mantle cell lymphoma?
A novel immune-related prognostic index (IRPI) provides better risk stratification and overall survival prediction than traditional MIPI scores in patients with mantle cell lymphoma.
The mantle cell lymphoma (MCL) International Prognostic Index (MIPI) and combined MIPI (MIPI-c) are commonly used for risk classification of MCL patients. However, these indexes lack immune-related parameters. The purpose of this study was to develop a novel prognostic model that integrated clinical and immune parameters. A total of 189 patients with newly diagnosed MCL from January 2010 to June 2020 were enrolled in our study. A nomogram and immune-related prognostic index (IRPI) were established to predict the overall survival (OS) of patients according to univariate and multivariate analyses. Discrimination and calibration were used to compare the prognostic performance of the IRPI, MIPI, and MIPI-c. External validation was performed based on validation dataset (n = 150) from two other centers. The results for the training dataset indicated that B symptoms, platelet count, B2M level, CD4+ T-cell count<26.7% and CD8+ T-cell count>44.2% were predictors for OS. All the prognostic factors were integrated into the nomogram. For the overlap of confidence intervals of each variable, we assigned one point for each factor. The IRPI categorized patients into three risk categories: a score of zero indicated low risk, a score of one or two indicated intermediate risk, and a score of ≥3 indicated high risk. The IRPI showed better discrimination and calibration power than the MIPI and MIPI-c in the training dataset and validation dataset. The novel IRPI is a refined risk stratification index and reflects the strong complementary prognostic effects between clinical and immune parameters in MCL.
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Lv et al. (2022) conducted an observational in Mantle cell lymphoma (MCL) (n=339). Immune-related prognostic index (IRPI) vs. MIPI and MIPI-c was evaluated on Overall survival. A novel immune-related prognostic index incorporating clinical factors and T-cell counts (CD4+ <26.7% and CD8+ >44.2%) showed better discrimination for overall survival than MIPI and MIPI-c.
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