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Table 7 Overview of different combination studies with VPA and AZA

From: Treatment of poor-risk myelodysplastic syndromes and acute myeloid leukemia with a combination of 5-azacytidine and valproic acid

Patient

This study

Soriano et al.

Voso et al.

Raffoux et al.

Craddock et al.

Drugs

VPA, 5-Aza

VPA, Aza, ATRA

VPA, Aza, ATRAa

VPA, Aza, ATRA

VPA, Aza, ATRA, theophylline

Dosage VPA

Median dosage 25 mg/kg continuously

50–75 mg/kg 7 days

600–1,500 mg continuously

35–50 mg/kg 7 days

ng

Dosage AZA

100 mg/m2 5 days

75 mg/m2 7 days

75 mg/m2 7 days

75 mg/m2 7 days

75 mg/m2 5 days

No. of pts.

n = 25, evaluable 24

n = 53

n = 62, 26 evaluableb

n = 65

n = 45

Median age

73 years

69 years

70 years

72 years

66 years

No. AML/MDS

75%/25%c

92%/8%

31%/69%d

85%/15%

80%/20%

Pretreatment

n = 10 (42%)

n = 20 (38%)

ng

n = 13 (20%)

n = 30 (67%)

ORR

37%

27%e

31%

26%

33%

CR/PR/HI/marrow response

7/2/0/4

27/0/0/7

3/5/4/ng

14/3/ngf/ng

7/8/ng/ng

Median cycles to response

2 (1–9)

2 (1–3)

5 (2–10) monthsg

ng

2 (1–6)

OS

9 months (23 in responders)

6.5 months (14+ in responders)

14.4 months

12.4 months (19.5 in responders)

ng

  1. ng not given
  2. aonly in non-responders
  3. bat least 8 cycles to be evaluable
  4. c46%/54% according to FAB
  5. d100% according to FAB
  6. e42% including marrow response
  7. f12.5% of non-responders had HI-erythroid
  8. gTime to CR