Table 2.
Dose reduction or delay after cycle 2
| First cycle | Reduction after cycle 2, n (%) | |||||
| G-CSF type | N | No | Yes | |||
| Overall | 234 | 198 (84.6) | 36 (15.4) | |||
| No G-CSF administration | 60 | 52 (86.7) | 8 (13.3) | |||
| Daily G-CSF | 122 | 104 (85.2) | 18 (14.8) | |||
| Pegfilgrastim | 52 | 42 (80.8) | 10 (19.2) | |||
|
Multivariate analysis a: Dose reduction Objective variable (0: no reduction, 1: dose reduction) |
Parameter estimate | Standard error | Odds ratio | p value | ||
| OR | 95% CI | |||||
| FN onset in cycle 1 (absent, present) | 1.7488 | 0.4672 | 5.748 | 2.301, 14.359 | 0.0002 | |
| Sex (male, female) | 0.9693 | 0.4122 | 2.636 | 1.175, 5.914 | 0.0187 | |
| Delay after cycle 2, n (%) | ||||||
| No | Yes | |||||
| Overall | 234 | 137 (58.5) | 97 (41.5) | |||
| No G-CSF administration | 60 | 36 (60.0) | 24 (40.0) | |||
| Daily G-CSF | 122 | 68 (55.7) | 54 (44.3) | |||
| Pegfilgrastim | 52 | 33 (63.5) | 19 (36.5) | |||
|
Multivariate analysis b: Dose delay Objective variable (0: absence of delay, 1: presence of delay) |
Parameter estimate | Standard error | Odds ratio | p value | ||
| OR | 95% CI | |||||
| Hemoglobin (≥ 12 g/dL, < 12 g/dL) | 0.8496 | 0.2801 | 2.339 | 1.351, 4.050 | 0.0024 | |
CI confidence interval, G-CSF granulocyte colony-stimulating factor, OR odds ratio
aVariables significantly associated with dose reduction were selected (p = 0.05)
bVariables significantly associated with dose delay were selected (p = 0.05), the final model by stepwise selection