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Natural killer cell activity is a risk factor for the recurrence risk after curative treatment of hepatocellular carcinoma

Authors
Lee, Han AhGoh, Hyun GilLee, Young-SunJung, Young KulKim, Ji HoonYim, Hyung JoonLee, Min-GooAn, HyungginJeen, Yoon TaeYeon, Jong EunByun, Kwan SooSeo, Yeon Seok
Issue Date
12-6월-2021
Publisher
BMC
Keywords
Natural killer cell; Interferon-gamma; Hepatocellular carcinoma; Stage; Recurrence
Citation
BMC GASTROENTEROLOGY, v.21, no.1
Indexed
SCIE
SCOPUS
Journal Title
BMC GASTROENTEROLOGY
Volume
21
Number
1
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/127849
DOI
10.1186/s12876-021-01833-2
ISSN
1471-230X
Abstract
Background: Natural killer (NK) cells have been known to contribute to surveillance and control of hepatocellular carcinoma (HCC). However, the association of NK cell activity with stage and recurrence risk of HCC have not been fully evaluated. Methods: Untreated patients with newly diagnosed HCC were prospectively enrolled. Peripheral blood mononuclear cells were isolated at the time of diagnosis. Patients who had undergone surgery or radiofrequency ablation were classified as the curative treatment group, and their blood samples were collected again at 1 month after treatment. Results: A total of 80 patients with HCC were enrolled. The mean age was 62.5 years. At baseline, interferon (IFN)-gamma producing NK cell proportion was significantly lower in patients with Barcelona clinic liver cancer (BCLC) stage B, C, or D than in those with BCLC stage 0 (42.9% vs. 56.8%, P = 0.045). Among all patients, 56 patients had undergone curative treatment, and 42 patients re-visited at 1 month after curative treatment. There was no significant change in total NK cell and IFN-gamma producing NK cell proportion from baseline to 1 month after treatment (all P > 0.05). During a median follow-up of 12.4 months, HCC recurred in 14 patients (33.3%). When patients were classified according to the IFN-gamma producing NK cell proportion (group 1, >= 45%; and group 2, < 45%), HCC recurrence rate did not differ according to the IFN-gamma producing NK cell proportion at baseline (log-rank test, P = 0.835). However, patients with < 45% IFN-gamma producing NK cell proportion at 1 month after treatment had a significantly higher HCC recurrence rate than patients with that of >= 45% (log-rank test, P < 0.001). Multivariate analysis revealed that BCLC stage B (hazard ratio [HR] = 3.412, P = 0.045) and < 45% IFN-gamma producing NK cell proportion at 1 month after treatment (HR = 6.934, P = 0.001) independently predicted an increased risk of HCC recurrence. Conclusions: Decreased NK cell activity is significantly associated with the advanced stage of HCC, and the increased recurrence risk of HCC after curative treatment.
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