Molecular subtype | Immuno phenotype | Presume d cell of origin | Diagnostic molecular features | Etiology | Frequencya | Clinical features |
---|---|---|---|---|---|---|
T/HRLBCL | CD20, CD45,k (CD79A/B), CD15—, (CD30—), | Progenitor cell of germinal center B- cell | Gene expression profiling | Unknown | ~1–4 % | Median age: 30–50 |
Gender dominance: male | ||||||
Extranodal (vague nodularity is rare) | ||||||
BOB1, PU.1+/—, CT2, PAX5, (BCL2), BCL6, IRF4— | Diffuse pattern with predominance of reactive T cells | |||||
Bone marrow involvement: ~ 30Â % | ||||||
Survival ~ 50 % at 5 years | ||||||
Curable ~ 45 % | ||||||
GCB- | CD20, CD10, CD22, (CD30), (BCL2), (MYC), BCL6, GCET, HGAL, LMO2, PTEN+/—, IRF4—, FOX —, | Germinal center B-cell | Gene expression profiling | Unknown | ~17 % | Median age 61 |
DLBCL | Gender dominance: male ≥ female | |||||
Nodal and extranodal | ||||||
Bone marrow involvement: ~ 15Â % | ||||||
Survival ~ 60 % at 5 years | ||||||
Curable ~ 50 % | ||||||
ABC- | CD20, CD22, (CD30), (CD79A/B), IRF4, FOXP1, (BCL2), (MYC), BCL6+/—, GCET—, LMO2—, | Post-germinal center B- cell | Gene expression profiling | Unknown | ~15 % | Median age: 66 |
DLBCL | Gender dominance: male ≥ female | |||||
Nodal and extranodal | ||||||
Bone marrow involvement: ~ 15Â % | ||||||
Survival ~ 40 % at 5 years | ||||||
Curable ~30Â % | ||||||
PMLBCL | CD19, CD20, CD22, CD30, CD45, CD79A, CD3—, CD10—, CD21— BOB1, PU.1, OCT2, PAX5, BCL6, IRF4, c-REL, TRAF1 | Post- thymic B- cell | Gene expression profiling | Unknown | ~6 % | Median age: 33 |
Gender dominance: female Mediastinal, thoracic > nodal Bone marrow involvement: rare Survival: > 60Â % at 5Â years | ||||||
Curable: > 60Â % |