Table 5.
Dose reduction | Dose delay | Treatment interruptiona | ||||
---|---|---|---|---|---|---|
OR (95% CI) | P value | OR (95% CI) | P value | OR (95% CI) | P value | |
GSTP1 c.313A>G | ||||||
AA | Reference | Reference | Reference | |||
AG | 0.70 (0.28–1.57) | 0.36 | 0.35 (0.13–0.90) | 0.03 | 0.35 (0.10–1.23) | 0.10 |
GG | 0.31 (0.09–1.03) | 0.06 | 0.43 (0.13–1.46) | 0.18 | 0.60 (0.14–2.58) | 0.49 |
Dominant (AA vs. AG + GG) | 0.54 (0.25–1.16) | 0.12 | 0.36 (0.16–0.85) | 0.02 | 0.42 (0.15–1.20) | 0.11 |
Recessive (AA + AG vs. GG) | 0.38 (0.13–1.16) | 0.08 | 0.68 (0.22–2.12) | 0.51 | 0.93 (0.23–3.73) | 0.92 |
ABCB1 c.1236C>T | ||||||
CC | Reference | Reference | Reference | |||
CT | 1.14 (0.36–3.64) | 0.82 | 1.00 (0.28–3.54) | 0.99 | 1.42 (0.28–7.26) | 0.67 |
TT | 3.33 (0.57––19.49) | 0.18 | 1.54 (0.24–9.71) | 0.64 | 2.03 (0.20–21.07) | 0.55 |
Dominant (CC vs. CT + TT) | 1.16 (0.39–3.45) | 0.78 | 1.08 (0.32–3.63) | 0.90 | 1.60 (0.32–7.90) | 0.57 |
Recessive (CC + CT vs. TT) | 3.08 (0.66–14.34) | 0.15 | 1.71 (0.38–7.63) | 0.48 | 1.73 (0.27–11.18) | 0.56 |
ABCB1 c.3435C>T | ||||||
CC | Reference | Reference | Reference | |||
CT | 0.89 (0.28–2.77) | 0.84 | 1.80 (0.51–6.31) | 0.36 | 1.70 (0.34–8.44) | 0.51 |
TT | 0.51 (0.07–3.42) | 0.49 | 0.96 (0.12–7.69) | 0.98 | 1.12 (0.07–15.90) | 0.93 |
Dominant (CC vs. CT + TT) | 0.95 (0.32–2.83) | 0.92 | 1.67 (0.48–5.79) | 0.42 | 1.55 (0.31–7.75) | 0.59 |
Recessive (CC + CT vs. TT) | 0.52 (0.10 2.68) | 0.43 | 0.52 (0.09–2.83) | 0.45 | 0.63 (0.07–5.50) | 0.68 |
CI, Confidence interval; OR, odds ratio.
Odds ratios was adjusted for age, histological subtypes, and International Federation of Gynecology and Obstetrics (FIGO); category bold values indicate statistically significant differences.
Cases of permanent discontinuation of the originally prescribed standard chemotherapy protocol (carboplatin and paclitaxel) or one of chemotherapeutic drug.