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Adjuvant Immunotherapy With Autologous Cytokine-Induced Killer Cells for Hepatocellular Carcinoma

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dc.contributor.authorLee, Joon Hyeok-
dc.contributor.authorLee, Jeong-Hoon-
dc.contributor.authorLim, Young-Suk-
dc.contributor.authorYeon, Jong Eun-
dc.contributor.authorSong, Tae-Jin-
dc.contributor.authorYu, Su Jong-
dc.contributor.authorGwak, Geum-Youn-
dc.contributor.authorKim, Kang Mo-
dc.contributor.authorKim, Yoon Jun-
dc.contributor.authorLee, Jae Won-
dc.contributor.authorYoon, Jung-Hwan-
dc.date.available2020-11-02T15:43:09Z-
dc.date.issued2015-06-
dc.identifier.issn0016-5085-
dc.identifier.issn1528-0012-
dc.identifier.urihttps://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/7856-
dc.description.abstractBACKGROUND & AIMS: No adjuvant therapy has been shown to extend the survival of patients with hepatocellular carcinoma (HCC) receiving curative treatment. We investigated whether injections of activated cytokine-induced killer (CIK) cells (CD3+/CD56+ and CD3+/CD56-T cells and CD3-/CD56+ natural killer cells) prolongs recurrence-free survival of patients after curative therapy for HCC. METHODS: We performed a multicenter, randomized, open-label, phase 3 trial of the efficacy and safety of adjuvant immunotherapy with activated CIK cells (created by incubation of patients' peripheral blood mononuclear cells with interleukin 2 and an antibody against CD3). The study included 230 patients with HCC treated by surgical resection, radiofrequency ablation, or percutaneous ethanol injection at university-affiliated hospitals in Korea. Patients were assigned randomly to receive immunotherapy (injection of 6.4 x 10(9) autologous CIK cells, 16 times during 60 weeks) or no adjuvant therapy (controls). The primary end point was recurrence-free survival; secondary end points included overall survival, cancer-specific survival, and safety. RESULTS: The median time of recurrence-free survival was 44.0 months in the immunotherapy group and 30.0 months in the control group (hazard ratio with immunotherapy, 0.63; 95% confidence interval [CI], 0.43-0.94; P = .010 by 1-sided log-rank test). Hazard ratios also were lower in the immunotherapy than in the control group for all-cause death (0.21; 95% CI, 0.06-0.75; P = .008) and cancer-related death (0.19; 95% CI, 0.04-0.87; P = .02). A significantly higher proportion of patients in the immunotherapy group than in the control group had an adverse event (62% vs 41%; P = .002), but the proportion of patients with serious adverse events did not differ significantly between groups (7.8% vs 3.5%; P = .15). CONCLUSIONS: In patients who underwent curative treatment for HCC, adjuvant immunotherapy with activated CIK cells increased recurrence-free and overall survival. ClinicalTrials.gov number: NCT00699816.-
dc.language영어-
dc.language.isoENG-
dc.publisherW B SAUNDERS CO-ELSEVIER INC-
dc.titleAdjuvant Immunotherapy With Autologous Cytokine-Induced Killer Cells for Hepatocellular Carcinoma-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1053/j.gastro.2015.02.055-
dc.identifier.scopusid2-s2.0-84930018607-
dc.identifier.wosid000355014700030-
dc.identifier.bibliographicCitationGASTROENTEROLOGY, v.148, no.7, pp 1383 - +-
dc.citation.titleGASTROENTEROLOGY-
dc.citation.volume148-
dc.citation.number7-
dc.citation.startPage1383-
dc.citation.endPage+-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusCD4(+) T-CELLS-
dc.subject.keywordPlusADOPTIVE IMMUNOTHERAPY-
dc.subject.keywordPlusANTITUMOR-ACTIVITY-
dc.subject.keywordPlusRECURRENCE RATES-
dc.subject.keywordPlusTUMOR-CELLS-
dc.subject.keywordPlusCIK CELLS-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusINTERLEUKIN-2-
dc.subject.keywordPlusCYCLOPHOSPHAMIDE-
dc.subject.keywordPlusIMMUNOBIOLOGY-
dc.subject.keywordAuthorLiver Cancer-
dc.subject.keywordAuthorClinical Trial-
dc.subject.keywordAuthorIL2-
dc.subject.keywordAuthorNK Cell-
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