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. 2020 Nov 20;4(22):5735–5744. doi: 10.1182/bloodadvances.2020002379

Table 2.

Comparison of idasanutlin trial patients with and without TP53 mutations

Characteristic Presence 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 5 12
 Mean ± SD 9.3 ± 3.20 14.4 ± 4.28
 Median 9 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