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首页> 外文期刊>Clinical & translational immunology. >Retrospective analysis of the efficacy of cytokine‐induced killer cell immunotherapy combined with first‐line chemotherapy in patients with metastatic colorectal cancer
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Retrospective analysis of the efficacy of cytokine‐induced killer cell immunotherapy combined with first‐line chemotherapy in patients with metastatic colorectal cancer

机译:重新试验杀伤细胞免疫治疗与转移结直肠癌患者的初级化疗结合的回顾性分析

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Objectives Fluoropyrimidine‐based chemotherapy regimens are the current first‐line treatment for metastatic colorectal cancer (mCRC); however, the outcome is often unsatisfactory. The present study aimed to determine the effect of combined cytokine‐induced killer (CIK) cell immunotherapy and first‐line chemotherapy in patients with mCRC. Methods This retrospective study included 252 patients with mCRC treated with first‐line chemotherapy. Among them, 126 patients received first‐line chemotherapy only (control group), while the other 126 patients, with similar demographic and clinical characteristics, received CIK cell immunotherapy combined with first‐line chemotherapy (CIK group). Overall survival (OS) and progression‐free survival (PFS) were compared between the two groups using the Kaplan–Meier method. Results The median OS for the CIK group was 54.7 versus 24.1?months for the controls, and the median PFS for the CIK group was 25.7 versus 14.6?months for the controls. Univariate and multivariate analyses indicated that CIK cell treatment was an independent prognostic factor for patients' OS and PFS. Subgroup analyses showed that CIK cell treatment significantly improved the OS and PFS of patients with metastatic colon cancer, but not those with metastatic rectal cancer. Additionally, the change in CD3sup+/supCD56sup+/sup subsets after the fourth treatment cycle might be an indicator of successful CIK cell treatment: Patients with increased CD3sup+/supCD56sup+/sup subsets had better survival than those with decreased CD3sup+/supCD56sup+/sup subsets. Conclusion Cytokine‐induced killer cell immunotherapy combined with first‐line chemotherapy could significantly improve the OS and PFS of patients with mCRC, particularly for patients with metastatic colon cancer.
机译:目的氟嘧啶基化疗方案是目前转移结直肠癌(MCRC)的第一线治疗;但是,结果往往不满意。本研究旨在确定细胞因子诱导的杀伤症(CIK)细胞免疫治疗和第一线化疗患者MCRC患者的影响。方法本回顾性研究包括252例患有一线化疗治疗的MCRC患者。其中,126名患者仅接受一线化疗(对照组),而另外126名患者,具有相似的人口统计和临床特征,接受CIK细胞免疫治疗联合一线化疗(CIK集团)。使用Kaplan-Meier方法比较两组之间的总存活(OS)和无进展生存(PFS)。结果CIK集团的中位操作系统为54.7与24.1个月的控制,CIK集团的中位数PFS为25.7与14.6个月为14.6个月。单变量和多变量分析表明CIK细胞治疗是患者OS和PFS的独立预后因素。亚组分析表明,CIK细胞治疗显着改善了转移性结肠癌患者的OS和PFS,但不是转移性直肠癌的患者。另外,第四治疗循环后CD3 + cd56 + 子集的变化可能是成功Cik细胞治疗的指标:CD3 + CD56 + 子集比CD3 + cd56 + 子集的子集更好地存活。结论细胞因子诱导的杀手细胞免疫治疗与一线化疗相结合,可显着改善MCRC患者的OS和PFS,特别是对于转移性结肠癌的患者。

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