Zhao Qun, Li Yong, Tan Bi-bo, Tian Yuan, Jiao Zhi-kai, Zhao Xue-feng, Zhang Zhi-dong, Wang Dong, Yang Pei-gang
Department of General Surgery, the Fourth Affiliated Hospital, Hebei Medical University, Shijiazhuang 050011, China.
Department of General Surgery, the Fourth Affiliated Hospital, Hebei Medical University, Shijiazhuang 050011, China. Email:
Zhonghua Zhong Liu Za Zhi. 2013 Oct;35(10):773-7.
The purpose of this study was to investigate the efficacy and mechanism of oxaliplatin in combination with capecitabine (XELOX) regimen as neoadjuvant chemotherapy in the treatment of patients with advanced gastric cancer.
Eighty-five patients with advanced gastric cancer (stage IIB and IIIC) were randomly divided into two groups: neoadjuvant chemotherapy group (40 cases) and surgery alone group (45 cases). In the neoadjuvant chemotherapy group, patients received oral administration of Xeloda 1000 mg/m(2) twice a day on days 1-14 and intravenous infusion of oxaliplatin 130 mg/m(2) on day 1 (XELOX regimen). The regimen was repeated every 21 days. In the surgery alone group, patients directly received radical resection of gastric cancer. The R0 resection rate, overall survival and disease free survival (DFS) were observed in all cases. The cycles and apoptosis rate of the gastric cancer cells were detected by flow cytometry. The expression of proliferating cell nuclear antigen (PCNA), p21, p53 and survivin was detected by Western blot.
In the neoadjuvant chemotherapy group, the total effective rate was 32.5% (13/40), and the tumor control rate was 90% (36/40), with few side effects. Compared with the surgery alone group, R0 resection rate was significantly higher in the neoadjuvant chemotherapy group (P < 0.05). The survival analysis indicated that both the overall survival and DFS were longer in the neoadjuvant chemotherapy group in comparison with those in the surgery alone group, but no significant differences were found (P > 0.05). In the neoadjuvant chemotherapy group, both the apoptosis rate and the ratio of cells in stage G0 and G1 were significantly higher than those in the surgery alone group (P < 0.05). The expression of PCNA and survivin was lower in the neoadjuvant chemotherapy group, while the expression of p21 and p53 was higher.
XELOX regimen as neoadjuvant chemotherapy in the treatment of patients with advanced gastric cancer can effectively improve the R0 resection rate and prolong the survival time of the patients. Its mechanism is probably that the neoadjuvant chemotherapy can markedly enhance apoptosis in gastric cancer cells and inhibit their proliferation.
本研究旨在探讨奥沙利铂联合卡培他滨(XELOX)方案作为新辅助化疗治疗晚期胃癌患者的疗效及机制。
85例晚期胃癌(IIB期和IIIC期)患者随机分为两组:新辅助化疗组(40例)和单纯手术组(45例)。新辅助化疗组患者于第1 - 14天口服希罗达1000 mg/m²,每日2次,第1天静脉输注奥沙利铂130 mg/m²(XELOX方案)。该方案每21天重复一次。单纯手术组患者直接接受胃癌根治性切除术。观察所有病例的R0切除率、总生存期和无病生存期(DFS)。采用流式细胞术检测胃癌细胞的周期及凋亡率。采用蛋白质免疫印迹法检测增殖细胞核抗原(PCNA)、p21、p53和生存素的表达。
新辅助化疗组总有效率为32.5%(13/40),肿瘤控制率为90%(36/40),副作用较少。与单纯手术组相比,新辅助化疗组的R0切除率显著更高(P < 0.05)。生存分析表明,新辅助化疗组的总生存期和DFS均长于单纯手术组,但差异无统计学意义(P > 0.05)。新辅助化疗组的凋亡率及G0期和G1期细胞比例均显著高于单纯手术组(P < 0.05)。新辅助化疗组PCNA和生存素的表达较低,而p21和p53的表达较高。
XELOX方案作为新辅助化疗治疗晚期胃癌患者可有效提高R0切除率,延长患者生存时间。其机制可能是新辅助化疗可显著增强胃癌细胞凋亡并抑制其增殖。