Table 2.

Cytogenetic abnormalities, latencies, and OS of patients with t-MNs after RT monotherapy

KaryotypeNumber of patients (%)Median latency, y (IQR)1-y OS % (95% CI)5-y OS % (95% CI)
Normal 26 (24%) 7.2 (3-10) 77 (62-95) 41 (25-66) 
Clonal abnormalities     
 Abnormal 5, 7, or both* 49 (45%) 6.6 (4-11) 37 (24-53) 2 (0-15) 
 Abnormal 5 22 4.4 (3-11) 36 (21-63) 5 (1-31) 
 Abnormal 7 11 6.6 (6-10) 46 (24-87) 
 Abnormal 5 and 7 16 6.5 (5-8) 31 (15-65) 
Recurring translocations 15 (14%) 2.3 (2-5) 55 (34-90) 55 (34-90) 
 t(8;21) 2.1 100 100 
 t(21q22) 3.7 
 t(15;17) 2.2 50 50 
 inv(16) 75 75 
 t(16;16) 2.3 100 100 
 t(11q23.3)/KMT2A 7.1 
 inv(3q) 35 100 NA 
Trisomy 8 11 (10%) 6.5 (4-15) 55 (32-94) 36 (17-80) 
Other clonal abnormalities 8 (7%) 12.9 (9-45) 63 (37-100) 13 (2-78) 
All cytogenetic analyses 109 6.5 (3-11) 52 (44-63) 22 (15-32) 
KaryotypeNumber of patients (%)Median latency, y (IQR)1-y OS % (95% CI)5-y OS % (95% CI)
Normal 26 (24%) 7.2 (3-10) 77 (62-95) 41 (25-66) 
Clonal abnormalities     
 Abnormal 5, 7, or both* 49 (45%) 6.6 (4-11) 37 (24-53) 2 (0-15) 
 Abnormal 5 22 4.4 (3-11) 36 (21-63) 5 (1-31) 
 Abnormal 7 11 6.6 (6-10) 46 (24-87) 
 Abnormal 5 and 7 16 6.5 (5-8) 31 (15-65) 
Recurring translocations 15 (14%) 2.3 (2-5) 55 (34-90) 55 (34-90) 
 t(8;21) 2.1 100 100 
 t(21q22) 3.7 
 t(15;17) 2.2 50 50 
 inv(16) 75 75 
 t(16;16) 2.3 100 100 
 t(11q23.3)/KMT2A 7.1 
 inv(3q) 35 100 NA 
Trisomy 8 11 (10%) 6.5 (4-15) 55 (32-94) 36 (17-80) 
Other clonal abnormalities 8 (7%) 12.9 (9-45) 63 (37-100) 13 (2-78) 
All cytogenetic analyses 109 6.5 (3-11) 52 (44-63) 22 (15-32) 

NA, not available.

*

Seventeen patients in this category also had loss of 17p.

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