Table 7.

Clonal Cytogenetic Abnormalities and ALL Immunophenotype

Abnormality B BMy T TMy B-LIN T-LINTotal
No. of cases  69  24  14  4  93  18 111  
t(9;22)7-150 13  10  0  0  23  0  23 
Any 11q23  14  1  0  0  15  0  15  
t(4;11) 12  1  0  0  13  0  13  
+21  9  4  1  13  1  14  
+8  7  3  0  0  10  10  
14q32  6  2  0  0  8  0  8  
−7 3  3  0  0  6  0  6  
del 9p  4  0  0  4  1  5  
Other abnormality  15  4  3  19  5  24  
Normal  15  6  10  1  21  11 32 
Abnormality B BMy T TMy B-LIN T-LINTotal
No. of cases  69  24  14  4  93  18 111  
t(9;22)7-150 13  10  0  0  23  0  23 
Any 11q23  14  1  0  0  15  0  15  
t(4;11) 12  1  0  0  13  0  13  
+21  9  4  1  13  1  14  
+8  7  3  0  0  10  10  
14q32  6  2  0  0  8  0  8  
−7 3  3  0  0  6  0  6  
del 9p  4  0  0  4  1  5  
Other abnormality  15  4  3  19  5  24  
Normal  15  6  10  1  21  11 32 

B-LIN combines B and BMy cases, whereas T-LIN combines T and TMy cases. Many patients were found to have more than one karyotypic abnormality and are therefore included in more than one category. Patients with t(8;14) were not included in this study.

F7-150

t(9;22) confirmed by cytogenetic analysis only. There were 4 B-LIN cases lacking cytogenetic evidence of t(9;22) that were BCR-ABL+. Additionally, 1 T-LIN case and 16 B-LIN cases were BCR-ABL+ but not evaluated cytogenetically.

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