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树突状细胞-细胞因子诱导的杀伤细胞免疫治疗联合紫杉醇-顺铂化疗治疗晚期卵巢癌的临床疗效分析。

Clinical efficacy analysis of Dendritic Cell-Cytokine Induced Killer Cell Immunotherapy Combined with Paclitaxel-Cisplatin Chemotherapy in patients with Advanced Ovarian Cancer.

机构信息

Department of Obstetrics and Gynecology, Affiliated Huai'an Hospital of Xuzhou Medical University and Second People's Hospital of Huai'an, Huai'an, China.

出版信息

J BUON. 2021 Mar-Apr;26(2):553-560.

Abstract

PURPOSE

To explore the efficacy and safety of dendritic cell-cytokine induced killer cell (DC-CIK) immunotherapy combined with paclitaxel-cisplatin chemotherapy in the treatment of advanced ovarian cancer.

METHODS

Patients with advanced ovarian cancer formed the Chemotherapy group (paclitaxel-cisplatin, n=68) and the other 68 patients formed the DC-CIK group (DC-CIK + paclitaxel-cisplatin, n=68). The short-term efficacy and changes in the levels of immune function indexes, serum CD133 and DEAD-box helicase 4 (DDX4) were analyzed.

RESULTS

Both overall response rate (ORR) and disease control rate (DCR) in the DC-CIK group were significantly better than those in the Chemotherapy group. After treatment, the proportions of CD3+ T lymphocytes, CD3+ CD4+ T lymphocytes and NK cells and the CD4/CD8 ratio were evidently higher, while the proportion of CD4+ CD25+ T lymphocytes was evidently lower in the DC-CIK group than those in the Chemotherapy group. After treatment, the levels of basic fibroblast growth factor (bFGF), carbohydrate antigen 19-9 (CA19-9), CA125, human epididymis protein 4 (HE4), cytokeratin 19 fragment antigen 21-1 (CYFRA21-1), DDX4 and CD133 markedly declined in the two groups, and they were markedly lower in the DC-CIK group than in the Chemotherapy group. At 1 month after treatment, the score of emotional functioning in function module of QLQ-C30 scale was greatly higher in the DC-CIK group than that in the Chemotherapy group, while the score of nausea and vomiting in symptom module was greatly lower in the DC-CIK group than that in the Chemotherapy group. The follow-up analysis showed that the overall survival (OS) rate in the DC-CIK group was remarkably superior than in the Chemotherapy group.

CONCLUSIONS

DC-CIK immunotherapy combined with paclitaxel-cisplatin chemotherapy can greatly improve the clinical efficacy, enhance the immune function, reduce the levels of serum tumor markers, raise the quality of life and prolong the survival in patients with advanced ovarian cancer.

摘要

目的

探讨树突状细胞-细胞因子诱导的杀伤细胞(DC-CIK)免疫治疗联合紫杉醇-顺铂化疗治疗晚期卵巢癌的疗效和安全性。

方法

将晚期卵巢癌患者分为化疗组(紫杉醇-顺铂,n=68)和 DC-CIK 组(DC-CIK+紫杉醇-顺铂,n=68)。分析两组近期疗效及免疫功能指标、血清 CD133 和 DEAD-box 解旋酶 4(DDX4)水平的变化。

结果

DC-CIK 组总缓解率(ORR)和疾病控制率(DCR)均明显优于化疗组。治疗后,DC-CIK 组 CD3+T 淋巴细胞、CD3+CD4+T 淋巴细胞和自然杀伤细胞比例及 CD4+/CD8+比值明显升高,CD4+CD25+T 淋巴细胞比例明显降低。治疗后,两组碱性成纤维细胞生长因子(bFGF)、糖类抗原 19-9(CA19-9)、CA125、人附睾蛋白 4(HE4)、细胞角蛋白 19 片段抗原 21-1(CYFRA21-1)、DDX4 和 CD133 水平均明显下降,且 DC-CIK 组明显低于化疗组。治疗 1 个月后,DC-CIK 组功能模块中生活质量量表(QLQ-C30)的情绪功能评分明显高于化疗组,而症状模块中的恶心呕吐评分明显低于化疗组。随访分析显示,DC-CIK 组总生存率(OS)明显优于化疗组。

结论

DC-CIK 免疫治疗联合紫杉醇-顺铂化疗可显著提高晚期卵巢癌患者的临床疗效,增强免疫功能,降低血清肿瘤标志物水平,提高生活质量,延长生存时间。

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