31 ± 0.61 vs. 10.16 ± 0.82, P < 0.0001, Fig. 1A). However, there was no significant difference in MPV values between the NSCLC patients with a high MPV/PC ratio BIBW2992 and the comparator group (10.00 ± 0.87 vs. 10.16 ± 0.82, P = 0.2191). In contrast, the PC was significantly increased in NSCLC patients with a low MPV/PC ratio compared to the comparator group (32.1 ± 7.1 vs. 21.7 ± 5.5, P < 0.0001, Fig. 1B). However, the PC was also slightly decreased in NSCLC patients with a low MPV/PC ratio compared to the comparator group (19.7 ± 3.8 vs. 21.7 ± 5.5, P = 0.0013). These findings suggest that NSCLC patients with a high MPV/PC ratio and the comparator group share similar characteristics
in terms of volume and number of platelets. However, the NSCLC patients with a low MPV/PC ratio were an independent group, not only from the comparator group but also from the group with a high
MPV/PC ratio, with respect to the kinetics of the circulating platelets. We conducted a series of survival analyses on June 1, 2013. At that time, 203 patients had died, 46 patients were lost to follow-up, and 19 patients were still alive. Consequently, the censoring rate was Selleck INCB024360 estimated at 24.3%. In univariate analyses, OS was significantly increased in patients who were women (P = 0.0018); those had never smoked (P = 0.0028); those with a PS of 0, 1, or 2 (P < 0.0001); and those with non-squamous cell carcinoma (P = 0.0003). However, clinical stage (P = 0.2390) and patient age (P = 0.5922) were not statistically significant ( Table 3). Protein kinase N1 We also analyzed the contribution of the MPV/PC ratio to OS. The MSTs were 10.3 months (95% CI: 7.7–13.1) and 14.5 months (95% CI: 10.0–18.6) for patients with low and high MPV/PC ratios, respectively ( Fig. 2). The 1-year survival rates were 43.8% (95% CI: 35.9–51.7) and 55.8% (95% CI: 44.5–66.1) for those with low and high MPV/PC ratios, respectively. In univariate analysis, OS was significantly decreased in the patients with a low MPV/PC ratio (P = 0.0245). We subsequently conducted a multivariate analysis to evaluate the independent survival impact of the covariates. Multivariate analysis
clearly revealed that a low MPV/PC ratio was an independent unfavorable prognostic factor for OS (hazard ratio [HR], 1.668, 95% CI: 1.235–2.271, P = 0.0008). In contrast, being female (P = 0.0009); having a PS of 0, 1, or 2 (P < 0.0001); having non–squamous cell carcinoma (P = 0.0027); and having stage IIIb disease (P = 0.0330) were independent favorable prognostic factors ( Table 4). Being younger than 70 years (P = 0.3697) was however not a significant factor. In contrast to the results of univariate analysis, no significant difference in OS was observed between patients with and without a history of smoking (P = 0.9325). These results suggest the presence of a confounding factor that that affects the impact of a smoking history. At present, evaluation of the MPV is attracting a great deal of interest.