Purpose: We performed detailed genomic analysis on 87 cases of diffuse large B-cell lymphoma of germinal center type (GCB DLBCL) to identify characteristics that are associated with survival in those treated with R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone).

Experimental Design: The cases were extensively characterized by combining the results of IHC, cell-of-origin gene expression profiling (GEP; NanoString), double-hit GEP (DLBCL90), FISH cytogenetic analysis for double/triple-hit lymphoma, copy-number analysis, and targeted deep sequencing using a custom mutation panel of 334 genes.

Results: We identified four distinct biologic subgroups with different survivals, and with similarities to the genomic classifications from two large retrospective studies of DLBCL. Patients with the double-hit signature, but no abnormalities of , and those lacking mutation and/or translocation, had an excellent prognosis. However, patients with an EZB-like profile had an intermediate prognosis, whereas those with inactivation combined with the double-hit signature had an extremely poor prognosis. This latter finding was validated using two independent cohorts.

Conclusions: We propose a practical schema to use genomic variables to risk-stratify patients with GCB DLBCL. This schema provides a promising new approach to identify high-risk patients for new and innovative therapies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923151PMC
http://dx.doi.org/10.1158/1078-0432.CCR-20-2378DOI Listing

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