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Updated: Jan 2, 2026

Enhancing Tumor Content through Tumor Macrodissection
Published on: February 12, 2022
Evaluation of the MD Anderson tumor score for diffuse large B-cell lymphoma in the rituximab era
Antonio Gutierrez1, Leyre Bento1, Antonio Diaz-Lopez2
1Lymphoma Unit, Department of Hematology, Hospital Universitari Son Espases/IdISBa, Palma, Spain.
Objectives:
Diffuse large B-cell lymphoma (DLBCL) is an aggressive heterogeneous lymphoma with standard treatment. However, 30%-40% of patients still fail, so we should know which patients are candidates for alternative therapies. IPI is the main prognostic score but, in the rituximab era, it cannot identify a very high-risk (HR) subset. The MD Anderson Cancer Center reported a score in the prerituximab era exclusively considering tumor-related variables: Tumor Score (TS). We aim to validate TS in the rituximab era and to analyze its current potential role.
Methods:
From GELTAMO DLBCL registry, we selected those patients homogeneously treated with R-CHOP (n = 1327).
Results:
Five-years PFS and OS were 62% and 74%. All variables retained an independent prognostic role in the revised TS (R-TS), identifying four different risk groups, with 5-years PFS of 86%, 71%, 50%, and very HR (28%). With a further categorization of three variables of the original TS (Ann Arbor Stage, LDH and B2M), we generated a new index that allowed an improvement in HR assessment.
Conclusions:
(a) All variables of the original TS retain an independent prognostic role, and R-TS remains predictive in the rituximab era; (b) R-TS and additional categorization of LDH, B2M, and AA stage (enhanced TS) increased the ability to identify HR subsets.
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