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Table 3 Age, sex, and ECOG status of patients in the 12 studies evaluated in the meta-analysis

From: Treatment outcomes for newly diagnosed, treatment-naïve TP53-mutated acute myeloid leukemia: a systematic review and meta-analysis

Study name (other identifier)

Sample size

Age, median (range)

Tx

Male, n (%)

ECOG status, n (%)

0

1

2

3

4

AZA-AML-001 [20]

241

75 (6)a

AZA

139 (57.7)

54 (22.4)

132 (54.8)

55 (22.8)

0

0

CALGB 11,002 [19]

82

72 (61–92)

DEC

51 (62.2)

22 (26.8)

41 (50.0)

16 (19.5)

3 (3.7)

Short 2019 [21]

28

77 (70–80)b

DEC 5-day

18 (64.3)

10 (35.7)

43

78 (69–82)b

DEC 10-day

30 (69.8)

13 (30.2)

VIALE-A [6]

145

76 (60–90)

AZA

87 (60.0)

81 (55.9)

64 (44.1)

286

76 (49–91)

VEN + AZA

172 (60.1)

157 (54.9)

129 (45.1)

DiNardo 2018 [22]

84

75 (61–90)

VEN + AZA

51 (60.7)

14 (16.7)

44 (52.4)

24 (28.6)

2 (2.4)

31

72 (65–86)

VEN + DEC

15 (48.4)

7 (22.6)

20 (64.5)

4 (12.9)

0

DiNardo 2020 [23]

37

74 (69–78)b

VEN + DEC

20 (54.1)

26 (70.3)

11 (29.7)

Kadia 2015 [24]

293

HDAC/HMA

Short 2020 [25]

202

70 (20–90)

IDAC- or HDAC-based/HMA ± VEN

Lindsley 2019 [26]

156

68 (4)a

7 + 3 cytarabine + daunorubicin

96 (61.5)

Prochazka 2019 [13]

98

57 (20–79)

IC

60 (61.2)

Chiche 2021 [27]

103

67 (20–83)

CPX-351 (daunorubicin + cytarabine)

54 (52.4)

Desoutter 2014 [28]

96

73 (44–88)

AZA

  1. AZA azacitidine, DEC decitabine, ECOG Eastern Cooperative Oncology Group, HDAC high-dose cytarabine, HMA hypomethylating agent, IC intensive chemotherapy, IDAC intermediate-dose cytarabine, IQR interquartile range, Tx treatment, VEN venetoclax
  2. aMean (± SD)
  3. bMedian (± IQR)