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. 2014 Nov 17;168(6):796–805. doi: 10.1111/bjh.13214

Table I.

Baseline patient and disease characteristics in patients treated with vosaroxin administered as a short (≤10 min) intravenous infusion

Schedule A* Schedule B Schedule C72 Schedule C90§ All patients
Patients treated, n 29 35 29 20 113
Median age (range), years 75 (61–89) 75 (64–87) 70 (61–84) 78 (66–88) 75 (61–89)
Gender, n (%)
 Male 19 (66) 23 (66) 14 (48) 17 (85) 73 (65)
 Female 10 (35) 12 (34) 15 (52) 3 (15) 40 (35)
AML subtype, n (%)
 With characteristic genetic abnormalities 0 2 (6) 2 (7) 1 (5) 5 (4)
 With multilineage dysplasia 12 (41) 8 (23) 6 (21) 9 (45) 35 (31)
 Alkylating agent–related AML and MDS 2 (7) 2 (6) 0 3 (15) 7 (6)
 Not otherwise categorized 15 (52) 22 (63) 19 (66) 7 (35) 63 (56)
 Missing 0 1 (3) 2 (7) 0 3 (3)
Adverse prognostic factors, n (%)
 Age ≥70 years 22 (76) 27 (77) 15 (52) 17 (85) 81 (72)
 AHD 11 (38) 10 (29) 7 (24) 7 (35) 35 (31)
 ECOG PS 2 4 (14) 4 (11) 9 (31) 3 (15) 20 (18)
 I/U cytogenetics 27 (93) 28 (80) 28 (97) 19 (95)** 102 (90)
 ≥2 risk factors 25 (86) 27 (77) 24 (83) 17 (85) 93 (82)

AHD, antecedent haematological disease; AML, acute myeloid leukaemia; ECOG PS, Eastern Cooperative Oncology Group performance status; I/U, intermediate/unfavourable; MDS, myelodysplastic syndrome.

*

72 mg/m2 on days 1, 8, and 15.

72 mg/m2 on days 1 and 8.

72 mg/m2 on days 1 and 4.

§

90 mg/m2 on days 1 and 4.

At diagnosis, by World Health Organization criteria (Vardiman et al, 2009).

**

Cytogenetic data are missing for one patient in this cohort.