Abstract

Our earlier multicenter randomized controlled trial showed that adjuvant immunotherapy with cytokine-induced killer (CIK) cells resulted in longer recurrence-free survival (RFS) and overall survival (OS) as well in patients who received curative treatment for hepatocellular carcinoma (HCC). In the present study, we determined if the efficacy of CIK cell therapy continued after end of repeated CIK cell injections. We performed a follow-up study of our preceding trial. We included 226 patients: 114 patients in the immunotherapy group (injection of 6.4 × 109 CIK cells, 16 times during 60 weeks) and 112 patients in the control group (no treatment) after potentially curative treatment for HCC. In total, 162 patients (89 of the immunotherapy group and 73 of controls) underwent an extended follow-up for 60 months after randomization of the last patient. The primary endpoint was RFS, and secondary endpoints included OS. During follow-up time of median 68.5 months (interquartile range 45.0–82.2 months), the immunotherapy group continued to show a significantly lower risk of recurrence or death [hazard ratio (HR) 0.67; 95% confidence interval (CI) 0.48–0.94; P = 0.009 by one-sided log-rank test]. At 5 years, RFS rate was 44.8% in the immunotherapy group and 33.1% in the control group. The risk of all-cause death was also lower in the immunotherapy group compared to the control group (HR 0.33; 95% CI 0.15–0.76; P = 0.006). In patients who received curative treatment for HCC, the significant improvement in RFS and OS as a result of adjuvant CIK cell immunotherapy lasted over 5 years without boosting.

Highlights

  • Liver cancer is the sixth most frequent cancer and the second leading cause of cancer-related mortality in the world [3]

  • Our group published the results of a multicenter, open-labeled, randomized controlled trial (RCT) demonstrating that adjuvant adoptive immunotherapy using autologous cytokine-induced killer (CIK) cells prolongs both recurrence-free survival (RFS) and overall survival (OS) after potentially curative treatment for hepatocellular carcinoma (HCC) [2]

  • The efficacy of CIK cell immunotherapy was analyzed for all 226 patients included in the original study

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Summary

Introduction

Liver cancer is the sixth most frequent cancer and the second leading cause of cancer-related mortality in the world [3]. Our group published the results of a multicenter, open-labeled, randomized controlled trial (RCT) demonstrating that adjuvant adoptive immunotherapy using autologous cytokine-induced killer (CIK) cells prolongs both recurrence-free survival (RFS) and overall survival (OS) after potentially curative treatment for HCC [2]. ­CD3+/CD56+ cells are scare in fresh human peripheral blood, and they are the main antitumor effector cells [12]. Patients who underwent adjuvant CIK cell immunotherapy (injection of autologous CIK cell agent 16 times during 60 weeks) had a significantly longer RFS compared to control patients (median 44.0 vs 30.0 months) with 37% lower risk of recurrence or death [hazard ratio (HR) 0.63; 95% confidence interval (CI) 0.43–0.94]. CIK cell immunotherapy was linked to a reduced risk of both all-cause death (HR 0.21; 95% CI 0.06–0.75) and cancer-related death (HR 0.19; 95% CI 0.04–0.87) [2]

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