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. 2017 Jun 22;6(7):1563–1572. doi: 10.1002/cam4.1121

Table 3.

Multivariate Cox proportional hazards regression analysis for 1‐year overall survival with inverse propensity score weighting (IPSW) adjustment

Variable Whole cohort EGFR‐TKI responder
No adjustment IPSW No adjustment IPSW
Erlotinib 1.32 (1.23–1.41) 1.10 (1.03–1.18) 1.22 (1.14–1.31) 1.08 (0.98–1.18)
Male 1.54 (1.44–1.65) 1.37 (1.29–1.45) 1.48 (1.38–1.60) 1.52 (1.40–1.65)
Age ≥ 65 years 1.17 (1.09–1.25) 1.18 (1.11–1.25) 1.09 (1.02–1.17) 1.22 (1.12–1.33)
EGFR‐TKI responder 0.22 (0.20–0.23) 0.21 (0.20–0.23) N/A N/A
Disease severity
Operation 0.59 (0.52–0.67) 0.63 (0.57–0.70) 0.59 (0.52–0.67) 0.63 (0.55–0.74)
Cachexia 1.37 (1.28–1.47) 1.26 (1.19–1.34) 1.30 (1.22–1.39) 1.40 (1.28–1.52)
Increased intracranial pressure 1.14 (1.06–1.22) 1.29 (1.21–1.36) 1.16 (1.08–1.25) 1.30 (1.19–1.42)
Duration of hospitalization (days) 1.001 (1.000–1.002) 1.001 (1.001–1.002)
Packed red blood cell transfusion 1.07 (1.06–1.08) 1.08 (1.07–1.09) 1.06 (1.05–1.07) 1.07 (1.05–1.08)

Multivariate Cox regression adjusted for gender, age, disease severity (operation, cachexia, increased intracranial pressure, duration of hospitalization [days], and transfusion), comorbidities (chronic obstructive pulmonary disease, diabetes mellitus, chronic kidney disease, tuberculosis, liver cirrhosis, autoimmune disease, transplantation, AIDS, and other malignancies), EGFR‐TKI responder, and low income.

Data were hazards ratio and 95% confidence interval.

EGFR‐TKIs, epidermal growth factor receptor‐tyrosine kinase inhibitors.