Table 2.

Comparison of idasanutlin trial patients with and without TP53 mutations

CharacteristicPresence of TP53 mutation
No (n = 7)Yes (n = 5)
Age, y   
 Mean ± SD 57.1 ± 13.50 63.9 ± 13.74 
 Median 61.7 65.6 
 Range 32.8, 69.5 49.0, 83.8 
Initial diagnosis, n (%)   
 Essential thrombocythemia 1 (14.3) 0 (0.0) 
 PV 6 (85.7) 5 (100.0) 
Sex, n (%)   
 Female 4 (57.1) 3 (60.0) 
 Male 3 (42.9) 2 (40.0) 
Disease duration (before study), mo   
 Mean ± SD 58.9 ± 32.43 58.6 ± 54.58 
 Median 60.9 43.9 
 Range 14.9, 94.2 21.0, 154.3 
HU intolerance/resistance, n (%)   
 HU-intolerant 5 (71.4) 3 (60.0) 
 HU-resistant 1 (14.3) 1 (20.0) 
 No exposure 1 (14.3) 1 (20.0) 
Planned dose cohort, n (%)   
 100 mg 5 (71.4) 1 (20.0) 
 150 mg 2 (28.6) 4 (80.0) 
Cycles, n   
 N 12 
 Mean ± SD 9.3 ± 3.20 14.4 ± 4.28 
 Median 14 
 Range 5.0, 14.0 9.0, 20.0 
Duration on study,wk   
 Mean ± SD 52.4 ± 38.36 77.7 ± 25.86 
 Median 36.3 85.1 
CharacteristicPresence of TP53 mutation
No (n = 7)Yes (n = 5)
Age, y   
 Mean ± SD 57.1 ± 13.50 63.9 ± 13.74 
 Median 61.7 65.6 
 Range 32.8, 69.5 49.0, 83.8 
Initial diagnosis, n (%)   
 Essential thrombocythemia 1 (14.3) 0 (0.0) 
 PV 6 (85.7) 5 (100.0) 
Sex, n (%)   
 Female 4 (57.1) 3 (60.0) 
 Male 3 (42.9) 2 (40.0) 
Disease duration (before study), mo   
 Mean ± SD 58.9 ± 32.43 58.6 ± 54.58 
 Median 60.9 43.9 
 Range 14.9, 94.2 21.0, 154.3 
HU intolerance/resistance, n (%)   
 HU-intolerant 5 (71.4) 3 (60.0) 
 HU-resistant 1 (14.3) 1 (20.0) 
 No exposure 1 (14.3) 1 (20.0) 
Planned dose cohort, n (%)   
 100 mg 5 (71.4) 1 (20.0) 
 150 mg 2 (28.6) 4 (80.0) 
Cycles, n   
 N 12 
 Mean ± SD 9.3 ± 3.20 14.4 ± 4.28 
 Median 14 
 Range 5.0, 14.0 9.0, 20.0 
Duration on study,wk   
 Mean ± SD 52.4 ± 38.36 77.7 ± 25.86 
 Median 36.3 85.1 
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