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Table 1 Mutation status in RAS and methylation status and clinical characteristics

From: Genomic and epigenomic predictors of response to guadecitabine in relapsed/refractory acute myelogenous leukemia

Characteristics

Mutation in RAS (n = 22)

No mutation in RAS (n = 100)

p value

Median age (range)

54 (29.1–81.7)

62 (23.4–86.1)

0.14

Sex

  

0.48

 Male (%)

15 (68%)

59 (59%)

 

 Female (%)

7 (32%)

41 (41%)

 

Cytogenetic risk

  

1

 Poor (%)

9 (41%)

42 (42%)

 

 Intermediate (%)

10 (45%)

50 (50%)

 

 Unevaluable (%)

3 (14%)

8 (8%)

 

PB blasts at screening (%), median (range)

58 (0–99)

5.5 (0–93)

< 0.0001

BM blasts at screening (%), median (range)

49 (18–95)

31.1 (2–94)

0.0005

Platelet count (K/μL) at screening, median (range)

31.5 (7–230)

36 (2–342)

0.44

Hemoglobin (g/dL) at screening, median (range)

9.4 (7.2–12.6)

9.3 (6.0–14.4)

0.96

WBC (K/μL) at screening, median (range)

9.5 (1.5–36.2)

2.1 (0.2–75.5)

0.0007

LINE-1 maximum demethylation %, mean ± SE*

18.9 ± 3.2

24.3 ± 1.3

0.056

IDH mutation

5 (23%)

18 (18%)

0.56

Methylation cluster

  

0.0009

 CIMP-like

10 (45%)

31 (31%)

 

 Intermediate

11 (50%)

24 (24%)

 

 Normal-like

0

40 (40%)

 

 Unknown

1 (5%)

5 (5%)

 

Response

 Complete CR rate (%)

0

15/100 (15%)

0.07

 CRc rate (%)

3/22 (14%)

23/100 (23%)

0.4

Median survival days (range)

129.5 (12–783+)

233 (7–1088+)

0.0004

2-year survival rate

1/22 (5%)

19/100 (19%)

0.12

  1. *Maximum LINE-1 demethylation for patients during the first cycle of guadecitabine treatment