Lei Changjiang, Ren Defa, Fu Meixia, Sun Chuantao, Ren Hong, Pan Qingyun, Li Yuan
Department of Oncological Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shanxi 710061, P.R. China.
Department of General Surgery, The Fifth Hospital of Wuhan, Wuhan, Hubei 430050, P.R. China.
Oncol Lett. 2019 Apr;17(4):3665-3670. doi: 10.3892/ol.2019.10022. Epub 2019 Feb 6.
Curative effect and adverse reactions of oxaliplatin combined with endostar in the interventional treatment of primary hepatic carcinoma (PHC) were investigated. A total of 101 PHC patients from October 2012 to December 2014 in The First Affiliated Hospital of Xi'an Jiaotong University were retrospectively collected. Fifty patients in combined therapy group were treated with oxaliplatin combined with endostar, while the remaining 51 patients in oxaliplatin group were treated with oxaliplatin alone. The treatment lasted for a total of 4 cycles (20 days as 1 cycle). The ratios of cluster of differentiation 3 (CD3), CD4 and CD8 were detected via enzyme-linked immunosorbent assay (ELISA). The objective response rate in combined therapy group was 92.00%, which was significantly higher than that in oxaliplatin group (74.51%). The main adverse reactions showed no statistical difference between the two groups (P>0.05). The median progression-free survival (PFS) was 8.6 months in combined therapy group and 6.3 months in oxaliplatin group, while the median overall survival (OS) was 12.9 months in combined therapy group and 10.6 months in oxaliplatin group. After treatment, CD4 and CD3 levels in the peripheral blood in both groups were obviously lower than those before treatment, but the CD8 level was obviously higher than that before treatment. At the same time, changes in the ratio of T lymphocyte subsets in combined therapy group were superior to those in oxaliplatin group, displaying statistically significant differences (P<0.05). Oxaliplatin combined with endostar has a good curative effect in the treatment of PHC with mild adverse reactions, which can prolong the survival time of patients, improve the levels of T lymphocyte subsets and increase the immunity of patients, so it is worthy of promotion and application in clinic.
探讨奥沙利铂联合恩度介入治疗原发性肝癌(PHC)的疗效及不良反应。回顾性收集2012年10月至2014年12月在西安交通大学第一附属医院就诊的101例PHC患者。联合治疗组50例患者采用奥沙利铂联合恩度治疗,其余51例奥沙利铂组患者仅接受奥沙利铂治疗。治疗共持续4个周期(20天为1个周期)。采用酶联免疫吸附测定(ELISA)检测分化簇3(CD3)、CD4和CD8的比例。联合治疗组的客观缓解率为92.00%,显著高于奥沙利铂组(74.51%)。两组主要不良反应无统计学差异(P>0.05)。联合治疗组的中位无进展生存期(PFS)为8.6个月,奥沙利铂组为6.3个月;联合治疗组的中位总生存期(OS)为12.9个月,奥沙利铂组为10.6个月。治疗后,两组外周血CD4和CD3水平均明显低于治疗前,但CD8水平明显高于治疗前。同时,联合治疗组T淋巴细胞亚群比例的变化优于奥沙利铂组,差异有统计学意义(P<0.05)。奥沙利铂联合恩度治疗PHC疗效良好,不良反应轻微,可延长患者生存时间,提高T淋巴细胞亚群水平,增强患者免疫力,值得临床推广应用。