Table 2.
Variable | |
---|---|
ORR, % | |
Total population (n = 15) | 47 |
Patients with high-risk cytogenetics (n = 5) | 40 |
Patients with intermediate-risk cytogenetics (n = 9) | 44 |
Best response achieved in overall patient population, n (%)* | |
CR | 3 (20) |
PR | 2 (13) |
HI | 2 (13) |
NR | 8 (53) |
Responses in high-risk cytogenetics group, n (%) | |
CR | 1 (20) |
PR | 0 (0) |
HI | 1 (20) |
NR | 3 (60) |
Responses in intermediate-risk cytogenetics group, n (%) | |
CR | 1 (11) |
PR | 2 (22) |
HI | 1 (11) |
NR | 5 (56) |
Median treatment duration, days (range) | 198 (13–724) |
Median time to best response, days (range) | 95 (44–279) |
Median OS, days (range) | |
Total population | 355 (13–908) |
Patients with high-risk cytogenetics | 167 (13–494) |
Patients with intermediate-risk cytogenetics | 401 (13–908) |
Responders to azacitidine | 532 (120–908) |
Patients maintaining ECOG PS of 0–2 during treatment, n (%) | 12 (80) |
Patients achieving independence from PRBC transfusion while receiving azacitidine, n (%) | 4 (26) |
Patients achieving independence from platelet transfusion while receiving azacitidine, n (%) | 6 (40) |
CR, complete remission; ECOG PS, Eastern Cooperative Oncology Group Performance Status; HI, hematologic improvement; ORR, overall response rate; OS, overall survival; PR, partial remission; PRBC, packed red blood cells.
Percentages do not total 100 because of rounding.