Table II.
ESA-naïve |
Prior ESA-treated |
|
---|---|---|
n = 144 | n = 62 | |
Patients eligible for target Hb analysis, n* | 129 | 57 |
KM (95% CL) percentage who reached target Hb† | 82% (70, 94) | 55% (40, 70) |
KM (95% CL) median time to achieve the target Hb, weeks | 7 (5, 9) | 24 (9, NE) |
Patients eligible for mean Hb analysis after target achieved, n‡ | 105 | 31 |
Mean (SD) Hb concentration of maintenance, g/l | 116 (8) | 117 (8) |
Median (Min, Max) Hb concentration of maintenance, g/l | 117 (99, 133) | 118 (101, 136) |
Mean Hb category after achieving target, n (%) | ||
Less than 110 g/l | 25 (24) | 8 (26) |
110–130 g/l | 75 (71) | 22 (71) |
Greater than 130 g/l | 5 (5) | 1 (3) |
ESA, erythropoiesis-stimulating agent; Hb, haemoglobin; KM, Kaplan–Meier; CL, confidence limits; Min, minimum; Max, maximum; NE, not estimable.
*Patients who had haemoglobin data either at baseline or after baseline were considered eligible except for those patients with baseline haemoglobin ≥110 g/l. Patients who had no haemoglobin data after baseline were counted as not having achieved the target level.
†Patients had to reach the target haemoglobin level (110 g/l) in the absence of a red blood cell transfusion within the preceding 28 d.
‡Patients who had baseline haemoglobin ≥110 g/l or who achieved the target haemoglobin concentration of 110 g/l were included.