Table 1.

Patient characteristics

AllMarrowBloodP
No. 77 35* 42  
Female (%) 30  (39) 10  (29) 20  (48) .089  
Age, y (range) 26  (16-59) 25  (17-53) 32  (16-59) .01  
Presentation leukocyte count (range) 7.6  (0.7-900) 12.2  (0.9-900) 4.4  (0.7-602) .65  
Karyotype (%)    .25  
 t(9;22) 6  (8) 4  (11) 2  (5)  
 t(4;11) 3  (4) 1  (3) 2  (5)  
 Other clonal 26  (34) 9  (26) 17  (40)  
 Normal 27  (35) 11  (31) 16  (38)  
 Not available 15  (19) 10  (29) 5  (12)  
CNS disease at presentation (%) 2  (3) 1  (3) 1  (2) .89  
Immunophenotype (%)    .11 
 Common 50  (65) 18  (51) 32  (76)  
 T 14  (18) 9  (26) 5  (12)  
 Null 8  (10) 4  (11) 4  (10)  
 B 3  (4) 3  (9)  
 Unknown 2  (3) 1  (3) 1  (2)  
Induction therapy (%)    < .0001  
 MRC UKALL X (or similar) 49  (63) 34  (97) 15  (36)  
 MRC UKALL XII (or similar) 28  (37) 1  (3) 27  (64)  
CR-transplantation interval, wk (range) 16  (1-90) 15  (5-69) 18  (1-90) .96 
Conditioning regimen (%)    < .0001 
 Melphalan-TBI 35  (45) 35  (100)   
 Melphalan alone 42  (55)  42  (100)  
AllMarrowBloodP
No. 77 35* 42  
Female (%) 30  (39) 10  (29) 20  (48) .089  
Age, y (range) 26  (16-59) 25  (17-53) 32  (16-59) .01  
Presentation leukocyte count (range) 7.6  (0.7-900) 12.2  (0.9-900) 4.4  (0.7-602) .65  
Karyotype (%)    .25  
 t(9;22) 6  (8) 4  (11) 2  (5)  
 t(4;11) 3  (4) 1  (3) 2  (5)  
 Other clonal 26  (34) 9  (26) 17  (40)  
 Normal 27  (35) 11  (31) 16  (38)  
 Not available 15  (19) 10  (29) 5  (12)  
CNS disease at presentation (%) 2  (3) 1  (3) 1  (2) .89  
Immunophenotype (%)    .11 
 Common 50  (65) 18  (51) 32  (76)  
 T 14  (18) 9  (26) 5  (12)  
 Null 8  (10) 4  (11) 4  (10)  
 B 3  (4) 3  (9)  
 Unknown 2  (3) 1  (3) 1  (2)  
Induction therapy (%)    < .0001  
 MRC UKALL X (or similar) 49  (63) 34  (97) 15  (36)  
 MRC UKALL XII (or similar) 28  (37) 1  (3) 27  (64)  
CR-transplantation interval, wk (range) 16  (1-90) 15  (5-69) 18  (1-90) .96 
Conditioning regimen (%)    < .0001 
 Melphalan-TBI 35  (45) 35  (100)   
 Melphalan alone 42  (55)  42  (100)  
*

Three patients with lymphoblastic lymphoma and bone marrow involvement who were included in our prior report have been excluded here.

Six patients had Ph+ disease detected on conventional cytogenetic studies (G-banding).

Reverse transcription–polymerase chain reaction was not performed routinely. It is therefore possible that the actual proportion of patients with Ph+ disease may be higher.

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