Department of Medical Oncology, the First Affiliated Hospital of University of Science and Technology of China (West), Heifei, Anhui, China.
Eur Rev Med Pharmacol Sci. 2018 Sep;22(17):5508-5518. doi: 10.26355/eurrev_201809_15811.
We analyzed the clinical observations of target arterial infusion of verapamil combined with chemotherapy as therapy for advanced gastric cancer.
From March 2012 to December 2015, a total of 63 patients with advanced gastric cancer were admitted to our department. The target artery in the control group was perfused with chemotherapy drugs only, and the target artery in the therapy group was injected with verapamil combined with chemotherapy drugs.
The therapeutic effect of the therapy group was significantly better than that of the control group in the primary foci of gastric cancer. Liver metastatic lesions: 11 patients in the control group had liver metastases and 25 patients in the therapy group had liver metastases. The effective rate (CR+PR) of the therapy group was significantly better than the control group. Clinical benefit evaluation: in the therapy group of 43 cases, 40 cases presented positive clinical benefit and 38 cases positive clinical weight in KFS scoring system; the clinical benefit of the therapy group was significantly better than control group. Survival analysis: the disease progression-free rate and survival rate of the therapy group were 12 months and 24 months, which were higher than those in the control group. The median PFS and median OS were also significantly longer than those in the control group (p<0.01). In the therapy group, adverse effects of chemotherapy in 43 patients were relieved in a short time.
Target arterial infusion of verapamil combined with chemotherapy drugs for advanced gastric cancer can significantly improve the efficacy of chemotherapy drugs and prolong the survival of patients.
我们分析了维拉帕米靶向动脉灌注联合化疗治疗晚期胃癌的临床观察。
2012 年 3 月至 2015 年 12 月,共有 63 例晚期胃癌患者入住我科。对照组的靶动脉仅灌注化疗药物,治疗组的靶动脉注入维拉帕米联合化疗药物。
治疗组对胃癌原发病灶的疗效明显优于对照组。肝转移病灶:对照组 11 例肝转移,治疗组 25 例肝转移。治疗组的有效率(CR+PR)明显优于对照组。临床获益评价:治疗组 43 例中,40 例有阳性临床获益,KFS 评分系统中 38 例有阳性临床体重;治疗组的临床获益明显优于对照组。生存分析:治疗组疾病无进展率和生存率为 12 个月和 24 个月,高于对照组。中位无进展生存期和中位总生存期也明显长于对照组(p<0.01)。在治疗组中,43 例患者的化疗不良反应在短时间内得到缓解。
维拉帕米靶向动脉灌注联合化疗药物治疗晚期胃癌可显著提高化疗药物的疗效,延长患者的生存时间。