Table 1.

Distribution of BCL-6 mutations throughout the spectrum of B-cell neoplasia

Histology BCL-6 Mutations (positive/tested)*
Precursor B-cell neoplasms  
 Acute lymphoblastic leukemia 0/46 (0%) (P < .001)  
Peripheral B-cell neoplasms  
 B-cell chronic lymphocytic leukemia 9/30 (30.0%)  
Small lymphocytic lymphoma  2/9 (22.2%) 
Lymphoplasmacytoid lymphoma  2/5 (40.0%)  
Mantle cell lymphoma  2/20 (10.0%) (P < .05)  
Follicular lymphoma  9/15 (60.0%)  
MALT lymphoma  5/15 (33.3%) 
Hairy cell leukemia  2/8 (25.0%)  
B-lineage diffuse large cell lymphoma 61/125 (48.8%)  
Burkitt lymphoma 13/35 (37.1%) 
Histology BCL-6 Mutations (positive/tested)*
Precursor B-cell neoplasms  
 Acute lymphoblastic leukemia 0/46 (0%) (P < .001)  
Peripheral B-cell neoplasms  
 B-cell chronic lymphocytic leukemia 9/30 (30.0%)  
Small lymphocytic lymphoma  2/9 (22.2%) 
Lymphoplasmacytoid lymphoma  2/5 (40.0%)  
Mantle cell lymphoma  2/20 (10.0%) (P < .05)  
Follicular lymphoma  9/15 (60.0%)  
MALT lymphoma  5/15 (33.3%) 
Hairy cell leukemia  2/8 (25.0%)  
B-lineage diffuse large cell lymphoma 61/125 (48.8%)  
Burkitt lymphoma 13/35 (37.1%) 
*

Statistically significant differences in BCL-6 mutation frequency are indicated by the corresponding P-value.

Cases of precursor B-cell acute lymphoblastic leukemia were representative of different molecular variants of the disease and included cases associated with hyperdiploidy (n = 5), rearrangement of BCR/ABL (n = 13), rearrangement of MLL (n = 9), rearrangement of TEL/AML-1 (n = 6), or no known genetic lesion (n = 13).

The representation of the different subsets of B-lineage diffuse large cell lymphoma included in this study is reported in Table 2.

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