Table 1.

Summary of p53 abnormalities in splenic lymphoma with villous lymphocytes obtained by different techniques

Abnormality: TechniquePatients studiedPatients with p53 abnormalities
AllUntreated prior to testingAllUntreated prior to testing
p53 deletion:     
 FISH 59 42 10 (17%) 8 (19%) 
p53 protein expression:     
 Immunocytochemistry 35/59* 22/42* 3 (9%)1-153 3 (13.6%)1-153 
 Flow cytometry 20/35 15/22 2 (10%) 2 (13.3%) 
p53 mutations:     
 Direct sequencing 9/11 8/9 2 (22%) 2 (25%) 
Abnormality: TechniquePatients studiedPatients with p53 abnormalities
AllUntreated prior to testingAllUntreated prior to testing
p53 deletion:     
 FISH 59 42 10 (17%) 8 (19%) 
p53 protein expression:     
 Immunocytochemistry 35/59* 22/42* 3 (9%)1-153 3 (13.6%)1-153 
 Flow cytometry 20/35 15/22 2 (10%) 2 (13.3%) 
p53 mutations:     
 Direct sequencing 9/11 8/9 2 (22%) 2 (25%) 

FISH indicates fluorescence in situ hybridization.

*

Cytospins available in 35 of 59 (22 of 42 for untreated) patients in whom FISH was performed.

Cells for flow cytometry available in 20 of 35 (15 of 22 for untreated) analyzed by immunocytochemistry.

DNA available in 9 of 11 (8 of 9 for untreated) patients with p53 deletion and/or p53 protein accumulation.

F1-153

Protein expression was found in 2 of 10 (2 of 8 for untreated) patients with a p53 deletion, one patient had protein expression without accompanying deletion and was only tested by immunocytochemistry.

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