Figure 2.
Validation of 30-gene risk model for ABC–DLBCL (activated B-cell–like diffuse large B-cell lymphoma) in population and clinical trial cohorts. The risk model was tested with survival restricted to 3 years. (A) The 30-gene signature distinguished high- and low-risk groups in the REMoDL-B clinical trial,7 (B) the R-CHOP arm of the Lymphoma/Leukemia Molecular Profiling Project (LLMPP) 2008 cohort,28 and (C) the Haematological Malignancy Research Network (HMRN) population study:29 red = high risk, blue = low risk. (D) Comparison of International Prognostic Index (IPI) scores and the risk groups defined using the linear predictor in the REMoDL-B cohort. (E) Comparison of genetic subcategories described by Lacy et al13 with risk groups defined using the linear predictor in the HMRN cohort. Of the 156 ABC cases in the HMRN data, the genomic subgroups were available for 98 cases.

Validation of 30-gene risk model for ABC–DLBCL (activated B-cell–like diffuse large B-cell lymphoma) in population and clinical trial cohorts. The risk model was tested with survival restricted to 3 years. (A) The 30-gene signature distinguished high- and low-risk groups in the REMoDL-B clinical trial,7 (B) the R-CHOP arm of the Lymphoma/Leukemia Molecular Profiling Project (LLMPP) 2008 cohort,28 and (C) the Haematological Malignancy Research Network (HMRN) population study:29 red = high risk, blue = low risk. (D) Comparison of International Prognostic Index (IPI) scores and the risk groups defined using the linear predictor in the REMoDL-B cohort. (E) Comparison of genetic subcategories described by Lacy et al13 with risk groups defined using the linear predictor in the HMRN cohort. Of the 156 ABC cases in the HMRN data, the genomic subgroups were available for 98 cases.

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