Fu Jian-Hong, Gao Zhan, Ren Chen-Chen, Shi Yong-Gang
Department of Obstetrics and Gynecology, Radiotherapy, The Fifth Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Asian Pac J Cancer Prev. 2013;14(4):2377-81. doi: 10.7314/apjcp.2013.14.4.2377.
A total of 285 patients with stage Ib2 and IIa2 cervical cancer were categorized into three groups, and received preoperative neoadjuvant chemotherapy combined with vaginal intracavitary irradiation, neoadjuvant chemotherapy alone or radiotherapy, respectively. The effective rate of 70.6 % in group 1 was much higher than 41.4% in group 2 (P=0.000) and 46.9 % in group 3 (P=0.000); The percentage of patients receiving postoperative adjuvant therapy was 44.1% in group 1, much lower than 67.8% in group 2 (P=0.001) and 64.6% in group 3 (P=0.004); The percentage of patients with no postoperative risk factor in group 1 was 52.0%, much higher than 32.2% in group 2 (P=0.006) and 35.4% in group 3 (P=0.019); The occurrence rate of surgery-related complications in groups 1, 2 and 3 were 29.4%, 28.7%, and 33.3%, respectively, with no statistical differences among the groups (P=0.981). Regarding preoperative neoadjuvant complications, none were obvious in group 3, while occurrence rates of myelosuppression in groups 1 and 2 were 89.1% and 86.6%, of nausea and vomitting were 78.4% and 78.2%, but without significant differences (all P>0.05). Among 166 patients who received postoperative adjuvant therapy in the three groups, the occurrence rates were: 65.4%, 64.3% and 61.1% respectively for myelosuppression; 42.3%, 38.1%, and 38.9% for nausea and vomiting; 9.6%, 9.5% and 9.7% for urocystitis; and 63.5%, 69.0% and 65.3% enteritis and rectitis. There were no statistically significant differences among them (all P>0.05). The five-year disease-free survival rates (DFS) in groups 1, 2, 3 were 78.3%, 75.1%, 80.9%, respectively; the five-year overall survival rates (OS) were 81.4%, 78.2%, and 81.1%, respectively. The five-year OS of 166 patients receiving postoperative in the three groups were 72.4%, 69.5%, and 71.8%, respectively, with no significant variation (all P>0.05). Although there were no differences among three groups in DFS and OS, preoperative neoadjuvant chemotherapy combined with intracavitary radiotherapy may increase the effective rate and the percentage of patients with no postoperative risk factors and decrease the percentage of patients receiving postoperative adjuvant therapy, thereby decreasing complications indirectly and increasing quality of life.
总共285例Ib2期和IIa2期宫颈癌患者被分为三组,分别接受术前新辅助化疗联合阴道腔内照射、单纯新辅助化疗或放疗。第1组的有效率为70.6%,远高于第2组的41.4%(P = 0.000)和第3组的46.9%(P = 0.000);第1组接受术后辅助治疗的患者百分比为44.1%,远低于第2组的67.8%(P = 0.001)和第3组的64.6%(P = 0.004);第1组无术后危险因素的患者百分比为52.0%,远高于第2组的32.2%(P = 0.006)和第3组的35.4%(P = 0.019);第1、2、3组手术相关并发症的发生率分别为29.4%、28.7%和33.3%,组间无统计学差异(P = 0.981)。关于术前新辅助化疗并发症,第3组无明显并发症,而第1组和第2组的骨髓抑制发生率分别为89.1%和86.6%,恶心呕吐发生率分别为78.4%和78.2%,但无显著差异(均P>0.05)。三组中接受术后辅助治疗的166例患者中,骨髓抑制发生率分别为65.4%、64.3%和61.1%;恶心呕吐发生率分别为42.3%、38.1%和38.9%;膀胱炎发生率分别为9.6%、9.5%和9.7%;肠炎和直肠炎发生率分别为63.5%﹑69.0%和65.3%。它们之间无统计学显著差异(均P>0.05)。第1、2、3组的五年无病生存率(DFS)分别为78.3%、75.1%、80.9%;五年总生存率(OS)分别为81.4%、78.2%和81.1%。三组中接受术后治疗的166例患者的五年OS分别为72.4%、69.5%和71.8%,无显著差异(均P>0.05)。虽然三组在DFS和OS方面无差异,但术前新辅助化疗联合腔内放疗可能会提高有效率和无术后危险因素患者的百分比,并降低接受术后辅助治疗患者的百分比,从而间接减少并发症并提高生活质量。