» Articles » PMID: 22916174

Adoptive Immunotherapy in Postoperative Hepatocellular Carcinoma: a Systemic Review

Overview
Journal PLoS One
Date 2012 Aug 24
PMID 22916174
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: The effectiveness of immunotherapy for postoperative hepatocellular carcinoma patients is still controversial. To address this issue, we did a systemic review of the literatures and analyzed the data with emphasis on the recurrence and survival.

Methods: We searched six randomized controlled trials that included adoptive immunotherapy in the postoperative management of hepatocellular carcinoma and compared with non-immunotherapy postoperation. A meta-analysis was carried out to examine one- and 3-year recurrence and survival.

Results: The overall analysis revealed significantly reduced risk of 1-year recurrence in patients receiving adoptive immunotherapy (OR=0.35; 95% CI, 0.17 to 0.71; p=0.003), in that the risk of 3-year recurrence with a pooled OR estimated at 0.31 (95% CI 0.16 to 0.61; p=0.001). However, no statistically significant difference was observed for 3-year survival between groups with adoptive immunotherapy and without adjuvant treatment (OR=0.91; 95% CI, 0.45 to 1.84; P=0.792).

Conclusions: Adjuvant immunotherapy with cytokine induced killer cells or lymphokine activated killer cells may reduce recurrence in postoperative hepatocellular carcinoma patients, but may not improve survival.

Citing Articles

Progression-Free Survival of a Patient with Advanced Hepatocellular Carcinoma Treated with Adoptive Cell Therapy Using Natural Killer Cells: A Case Report.

Hong G, Xie S, Guo Z, Zhang D, Ge S, Zhang S Onco Targets Ther. 2022; 15:255-266.

PMID: 35313527 PMC: 8934175. DOI: 10.2147/OTT.S344707.


A Five-Gene Signature for Recurrence Prediction of Hepatocellular Carcinoma Patients.

Wang Z, Zhang N, Lv J, Ma C, Gu J, Du Y Biomed Res Int. 2020; 2020:4037639.

PMID: 33163533 PMC: 7604585. DOI: 10.1155/2020/4037639.


Clinical Trials with Combination of Cytokine-Induced Killer Cells and Dendritic Cells for Cancer Therapy.

Garofano F, Gonzalez-Carmona M, Skowasch D, Schmidt-Wolf R, Abramian A, Hauser S Int J Mol Sci. 2019; 20(17).

PMID: 31484350 PMC: 6747410. DOI: 10.3390/ijms20174307.


Immunotherapy in Hepatocellular Carcinoma: Is There a Light at the End of the Tunnel?.

Mahipal A, Tella S, Kommalapati A, Lim A, Kim R Cancers (Basel). 2019; 11(8).

PMID: 31366113 PMC: 6721326. DOI: 10.3390/cancers11081078.


Combinational immune-cell therapy of natural killer cells and sorafenib for advanced hepatocellular carcinoma: a review.

Hosseinzadeh F, Verdi J, Ai J, Hajighasemlou S, Seyhoun I, Parvizpour F Cancer Cell Int. 2018; 18:133.

PMID: 30214375 PMC: 6131874. DOI: 10.1186/s12935-018-0624-x.


References
1.
Kanai T, Monden M, Takeda T, Gotoh M, Sakon M, Umeshita K . [Adoptive immunotherapy in patients with multiple hepatic cancers using lymphokine activated killer cells (LAK) and interleukin-2]. Gan To Kagaku Ryoho. 1993; 20(11):1457-60. View

2.
Tan A, Aucejo F, Kim R . Is there a role for adjuvant treatment after hepatic resection for hepatocellular carcinoma?. Oncology. 2010; 78(3-4):161-71. DOI: 10.1159/000315577. View

3.
Haruta I, Yamauchi K, Aruga A, Komatsu T, Takasaki K, Hayashi N . Analytical study of the clinical response to two distinct adoptive immunotherapies for advanced hepatocellular carcinoma: comparison between LAK cell and CTL therapy. J Immunother Emphasis Tumor Immunol. 1996; 19(3):218-23. DOI: 10.1097/00002371-199605000-00006. View

4.
Lafreniere R, Rosenberg S . Successful immunotherapy of murine experimental hepatic metastases with lymphokine-activated killer cells and recombinant interleukin 2. Cancer Res. 1985; 45(8):3735-41. View

5.
Llovet J, Bruix J . Systematic review of randomized trials for unresectable hepatocellular carcinoma: Chemoembolization improves survival. Hepatology. 2003; 37(2):429-42. DOI: 10.1053/jhep.2003.50047. View