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Gun-Chil-Jung 联合细胞因子诱导的杀伤细胞免疫治疗用于终末期肝细胞癌患者的可行性:一例病例报告

英文原题:Feasibility of combination of Gun-Chil-Jung and cytokine-induced killer cells-based immunotherapy for terminal hepatocellular carcinoma patient: a case report.

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Feasibility of combination of Gun-Chil-Jung and cytokine-induced killer cells-based immunotherapy for terminal hepatocellular carcinoma patient: a case report.

PubMed 2023/08/30(内容时间) Front Pharmacol Q1 · IF 5.4(JCR 2025)

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中文摘要

患者的总生存期、肿瘤标志物水平、ECOG 分级及症状,包括腹水、下肢水肿、黄疸、胸腔积液和乏力,均得到大幅缓解。

我们期望这种联合治疗可能成为终末期 HCC 姑息治疗的一种选择。

展开英文摘要原文

Introduction: Terminal-stage hepatocellular carcinoma (HCC) is inoperable and currently has no form of adjuvant therapy.

This study examined the anticancer herbal extract Gun-Chil-Jung (GCJ) combined with cytokine-induced killer (CIK)-cell-based immunotherapy as a palliative therapy for terminal HCC.

We report the case of an HCC patient with extended overall survival and improved symptoms and tumor marker levels following combination therapy with GCJ and CIK cell-based immunotherapy. Baseline Characteristics: From March to July 2020, a 57-year-old man who had been diagnosed with HCC underwent combination treatment with GCJ and CIK cell-based immunotherapy. By August 2021, he was prescribed GCJ.

After treatment, the patient's condition was evaluated with respect to overall survival, tumor markers, symptoms, abdominal computed tomography findings, chest x-ray results, and Eastern Cooperative Oncology Group (ECOG) grade. Results: The patient's overall survival, tumor marker levels, ECOG grade, and symptoms, including ascites, lower limb edema, jaundice, pleural effusion, and fatigue, were largely alleviated. Conclusion: We expect that this combination therapy may be an option for palliative therapy of terminal HCC.

论文信息

作者
Park CR、Bae HR、Lee GY、Son CG、Cho JH、Cho CK、Lee NH
单位
Department of Hepatology and Hematology, Graduated School of Korean Medicine, Daejeon University, Daejeon, Republic of Korea.South Korea
文献类型
病例报告
期刊
Frontiers in pharmacology2023
原文标识
PubMed 37719842 · DOI 10.3389/fphar.2023.1203379