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. 2021 Feb 8;10:610820. doi: 10.3389/fonc.2020.610820

Table 3.

Outcomes of patients with AML treated with venetoclax combination strategies according to TP53 mutation status.

Study No1 of pts6 Type of AML2 Pts6 with mutated TP53 (%) Type of treatment Overall Response Duration of response Overall survival
No of patients (%) Median time (months/range) Median time (months/range)
Di Nardo et al. (64) 145 145 (100%) de novo AML2 36 (25) 73 (51%) pts6 received VEN3 plus DAC4; 72 (49%) VEN plus AZA5 17 (47) 5.2 (1.2–9.4) 7.2 (3.7–NR11)
Bejar et al. (47) 31 15 (49%) de novo AML2; 16 (51%) R/R8 AML2 31(100) 28 (90%) pts6 received VEN3 plus DAC4; 3 (10%) VEN3 plus AZA5 16 (52)
67% in de novo AML2 vs. 38% in R/R8 AML2 (p = 0.01)
NR7 NR7
Shoulker et al. (70) 69 36 (52%) de novo AML2; 33 (48%) R/R8 AML2 69 (100) 60 (87%) pts6 received VEN3 plus DAC4 or AZA5; 2 (3%) VEN3 plus FLAG-ida9; 3 (4%) VEN3 plus low dose Ara-C10; 5 (6%) VEN3 plus CPX-351 25 (36)
47% in de novo AML2 vs. 24% in R/R8 AML2
6.4 months in de novo AML2 vs. 3.6 months in R/R8 AML2 3.6 months in de novo AML2 vs. 2.5 months in R/R8 AML2

1No, number; 2AML, acute myeloid leukemia; 3VEN, venetoclax; 4DAC, decitabine; 5AZA, azacitidine; 6pts, patients; 7NR, not reported; 8R/R, relapsed/refractory; 9FLAG-ida, fludarabine, cytarabine, G-CSF, idarubicin; 10ARA-C, cytarabine; 11NR, not reached.