Liang Xiaoyan, Wei Zhangfeng
Xiaoyan Liang, Collage of Pharmacy, Xi'an Medical University, Xi'an, Shaanxi 710021, P.R. China.
Zhangfeng Wei, Cardio-Thoracic Surgery, Xishan Coal Electricity Group Worker General Hospital, Taiyuan, Shanxi 030053, P.R. China.
Pak J Med Sci. 2021 Jul-Aug;37(4):1063-1068. doi: 10.12669/pjms.37.4.3820.
To evaluate the effect of sintilimab combined with chemotherapy on tumor markers and immune function in advanced non-small cell lung cancer.
The study was conducted at Xi'an Medical University, China. The 120 patients with advanced NSCLC who were treated in our hospital from January 2016 to January 2020 were randomly divided into two groups, with 60 cases in each group. Patients in the control group received conventional GP chemotherapy, while those in the experimental group received intravenous injection of sindilimab on the basis of conventional GP chemotherapy. The changes of serum tumor markers CYFRA211, CEA, CA125 and T lymphocyte subsets CD3+, CD4+, CD8+, CD4+/CD8+ in the two groups prior to and after treatment were compared and analyzed. At the same time, the clinical efficacy at six months was compared between the two groups.
The serum tumor markers CYFRA211, CEA and CA125 in the two groups after treatment were lower than those before treatment, and the difference was statistically significant (P=0.00). Specifically, the above-mentioned markers in the experimental group decreased more significantly than those in the control group, and the difference was statistically significant (CYFRA211, CA125, p=0.00; CEA, p=0.01; the levels of CD3+ and CD4+ in the experimental group were higher than those in the control group after treatment, with statistical significance (CD3+, p=0.00; CD4+, p=0.01)). No significant change can be seen in CD8+ (p=0.14), and the level of CD4+/CD8+ in the experimental group was higher than that in the control group, with a significant difference (p=0.02). The complete remission rate (CR) was 22% in the experimental group and 8% in the control group (P=0.04), which was statistically significant. The progress rate (PD) of the experimental group was significantly lower than that of the control group, with statistical significance (p=0.02). The overall response rate (RR) of the experimental group was more advantageous than that of the control group, with a statistically significant difference (p=0.01).
Compared with chemotherapy alone, significant therapeutic effects can be obtained in the treatment of advanced non-small cell lung cancer with sintilimab combined with chemotherapy. With this combination regimen, the level of serum tumor markers can be significantly reduced, the cellular immune function of patients can be improved, with the overall response rate of treatment increased, and the risk of progressive disease of patients reduced.
评估信迪利单抗联合化疗对晚期非小细胞肺癌患者肿瘤标志物及免疫功能的影响。
本研究在中国西安医学院进行。选取2016年1月至2020年1月在我院接受治疗的120例晚期非小细胞肺癌患者,随机分为两组,每组60例。对照组接受常规GP化疗,试验组在常规GP化疗基础上静脉注射信迪利单抗。比较分析两组治疗前后血清肿瘤标志物CYFRA211、CEA、CA125及T淋巴细胞亚群CD3+、CD4+、CD8+、CD4+/CD8+的变化。同时,比较两组治疗6个月时的临床疗效。
两组治疗后血清肿瘤标志物CYFRA211、CEA及CA125均低于治疗前,差异有统计学意义(P = 0.00)。具体而言,试验组上述标志物下降幅度较对照组更显著,差异有统计学意义(CYFRA211、CA125,P = 0.00;CEA,P = 0.01);试验组治疗后CD3+和CD4+水平高于对照组,差异有统计学意义(CD3+,P = 0.00;CD4+,P = 0.01)。CD8+无明显变化(P = 0.14),试验组CD4+/CD8+水平高于对照组,差异有统计学意义(P = 0.02)。试验组完全缓解率(CR)为22%,对照组为8%(P = 0.04),差异有统计学意义。试验组进展率(PD)显著低于对照组,差异有统计学意义(P = 0.02)。试验组总缓解率(RR)优于对照组,差异有统计学意义(P = 0.01)。
与单纯化疗相比,信迪利单抗联合化疗治疗晚期非小细胞肺癌可取得显著疗效。采用该联合方案可显著降低血清肿瘤标志物水平,改善患者细胞免疫功能,提高治疗总缓解率,降低患者疾病进展风险。