Skip to main content
. 2023 Sep 16;40(11):4928–4944. doi: 10.1007/s12325-023-02648-1

Table 2.

Summary of identified CINV risk factors based on multivariate analysis using backward elimination

Factor Overall (0–120 h) Acute (0–24 h) Delayed (24–120 h) Extended overall (0–168 h) Extended delayed (24–168 h) Beyond delayed (120–168 h)
OR (95% CI) p OR (95% CI) p OR (95% CI) p OR (95% CI) p OR (95% CI) p OR (95% CI) p
Overall population
Age (≥ 55/ < 55) 1.774 (1.062–2.962) 0.028
Sex (male/female) 1.528 (1.114–2.095) 0.009 2.434 (1.587–3.733) < 0.001 1.529 (1.110–2.107) 0.009 1.512 (1.111–2.059) 0.009 1.455 (1.063–1.991) 0.019
Performance status (0/1) 1.404 (1.097–1.798) 0.007 1.417 (1.102–1.823) 0.007 1.336 (1.049–1.701) 0.019 1.329 (1.040–1.697) 0.023
Drinking history (yes/no or rarely) 1.663 (1.283–2.155) < 0.001 1.854 (1.176–2.923) 0.008 1.746 (1.339–2.278) < 0.001 1.733 (1.348–2.227) < 0.001 1.780 (1.378–2.298) < 0.001
Smoking history (yes/no) 1.466 (1.038–2.069) 0.030 1.514 (1.068–2.145) 0.020 1.443 (1.028–2.025) 0.034 1.454 (1.032–2.047) 0.032
Motion sickness (no/yes) 1.524 (1.047–2.219) 0.028 1.750 (1.028–2.978) 0.039 1.659 (1.138–2.420) 0.009 1.521 (1.047–2.210) 0.028
Pregnancy-related vomiting (no/yes)
Cancer type (other/lung)
CDDP dose (< 80 mg/m2/ ≥ 80 mg/m2) 2.175 (1.417–3.338) < 0.001
NK-1RA (placebo/FosNTP 235 mg) 0.373 (0.262–0.531)  < 0.001 0.253 (0.146–0.438) < 0.001 0.365 (0.255–0.523) < 0.001 0.370 (0.261–0.523) < 0.001 0.370 (0.260–0.526) < 0.001
Treatment failure in 0–120 h (no/yes) 20.951 (14.407–30.466) < 0.001
FosNTP 235 mg group
Age (≥ 55/ < 55) 2.641 (1.126–6.191) 0.026
Sex (male/female)
Performance status(0/1)
Drinking history (yes/no or rarely) 2.017 (1.317–3.089) 0.001 2.172 (1.399–3.374) < 0.001 2.049 (1.359–3.090) < 0.001 2.177 (1.425–3.326) < 0.001
Smoking history (yes/no) 1.842 (1.144–2.967) 0.012 1.860 (1.149–3.012) 0.012 1.900 (1.194–3.022) 0.007 1.798 (1.120–2.886) 0.015
Motion sickness (no/yes) 1.901 (1.082–3.342) 0.026 2.045 (1.160–3.606) 0.013 1.785 (1.016–3.138) 0.044
Pregnancy-related vomiting (no/yes)
Cancer Type (other/lung)
CDDP dose (< 80 mg/m2/ ≥ 80 mg/m2) 2.659 (1.124–6.292) 0.026
Treatment failure in 0–120 h (no/yes) 34.184 (17.262–67.696) < 0.001
FosAPR group
Age (≥ 55/ < 55)
Sex (male/female) 3.479 (1.610–7.518) 0.002 2.351 (1.453–3.804) < 0.001 2.446 (1.498–3.994) < 0.001
Performance status (0/1)
Drinking history (yes/no or rarely)
Smoking history (yes/no) 2.160 (1.268–3.679) 0.005 2.434 (1.423–4.166) 0.001
Motion sickness (no/yes) 2.181 (1.049–4.534) 0.037 2.422 (1.159–5.061) 0.019 2.143 (1.023–4.489) 0.043
Pregnancy-related vomiting (no/yes)
Cancer type (other/lung)
CDDP dose (< 80 mg/m2/ ≥ 80 mg/m2)
Treatment failure in 0–120 h (no/yes) 16.437 (8.806–30.681) < 0.001

Data were obtained from the full analysis set

h hours, OR odds ratio, CI confidence interval, CDDP cisplatin, NK-1RA neurokinin 1 receptor antagonist, FosAPR fosaprepitant, FosNTP fosnetupitant