Hu Jin-long, Wu Ling-ying, Li Ning, Li Xiao-guang, Huang Man-ni, Zhang Rong
Department of Gynecologic Oncology, Cancer Institute & Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100021, China.
Zhonghua Fu Chan Ke Za Zhi. 2012 Jun;47(6):452-7.
To compare the clinical efficacy of neoadjuvant chemotherapy plus vaginal intracavitary irradiation, neoadjuvant chemotherapy alone and vaginal intracavitary irradiation alone followed by radical hysterectomy in patients with stage Ib2 and IIa2 bulkly cervical carcinoma.
Between January 2000 and December 2009, 224 patients with stage Ib2 and IIa2 bulkly cervical carcinoma (tumor diameter > 4 cm) received neoadjuvant therapy combined surgery in Cancer Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences were respectively analyzed, and they were divided into 3 groups according to the preoperative neoadjuvant therapy, the neoadjuvant chemotherapy combined vaginal intracavitary irradiation group (chemotherapy combined irradiation group, n = 86), the neoadjuvant chemotherapy alone group (chemotherapy group, n = 48), the vaginal intracavitary irradiation alone group (irradiation group, n = 90). The efficacy, postoperative risk factors, postoperative adjuvant therapy and survival were compared among the 3 groups.
Among the chemotherapy combined irradiation group, chemotherapy group and irradiation group, the response rate (RR) were respectively 62% (53/86), 42% (20/48) and 37% (33/90), and there was significant difference (P = 0.003). The comparison of deep stromal invasion, lymph node metastases, lympho-vascular space involvement (LVSI) and other risk factors among the 3 groups, which showed that there were no statistically significant differences (P > 0.05). In chemotherapy combined irradiation group, the percentage of stromal invasion ≥ 1/2 was lower than that in chemotherapy group [53% (46/86) vs. 73% (35/48), P = 0.027], and the percentage of lymph node metastases was significantly lower than irradiation group [17% (15/86) vs. 29% (26/90), P = 0.046], and the risk factors-free rate was significantly higher than chemotherapy group [44% (38/86)vs. 25% (12/48), P = 0.028]. Among the chemotherapy combined irradiation group, chemotherapy group and irradiation group, the percentage of postoperative radiation therapy were respectively 47% (40/86), 67% (32/48) and 62% (56/90), and the differences were statistically significant (P = 0.035). The five-year disease free survival (DFS) was 79%, 75% and 78%, respectively. The five-year overall survival (OS) was respectively 81%, 78% and 81% among 3 groups, and there were no statistically significant differences (P > 0.05). Among 224 patients, the five-year DFS of the patients with 0, 1 and ≥ 2 risk factors after surgery were 90%, 75% and 57%, and OS were 95%, 82% and 65%, and there were no statistically significant differences (P < 0.01, respectively). Of patients without postoperative risk factors, the five-year OS in those without receiving postoperative radiation therapy was 96%, while 89% in received postoperative radiation therapy patients, there were no statistically significant differences (P = 0.263).
There are no differences of DFS and OS among the neoadjuvant chemotherapy combined vaginal intracavitary irradiation group, the neoadjuvant chemotherapy alone group and the vaginal intracavitary irradiation alone group patients with stage Ib2 and IIa2. Patients without risk factors after neoadjuvant therapies have better prognosis.
比较新辅助化疗联合阴道腔内照射、单纯新辅助化疗以及单纯阴道腔内照射后行根治性子宫切除术治疗Ib2期和IIa2期巨块型宫颈癌患者的临床疗效。
2000年1月至2009年12月,中国医学科学院北京协和医学院肿瘤医院224例Ib2期和IIa2期巨块型宫颈癌(肿瘤直径>4 cm)患者接受新辅助治疗联合手术,根据术前新辅助治疗方法分为3组,新辅助化疗联合阴道腔内照射组(化疗联合照射组,n = 86)、单纯新辅助化疗组(化疗组,n = 48)、单纯阴道腔内照射组(照射组,n = 90)。比较3组的疗效、术后危险因素、术后辅助治疗及生存情况。
化疗联合照射组、化疗组和照射组的有效率(RR)分别为62%(53/86)、42%(20/48)和37%(33/90),差异有统计学意义(P = 0.003)。3组间深部间质浸润、淋巴结转移、脉管间隙浸润(LVSI)等危险因素比较,差异无统计学意义(P>0.05)。化疗联合照射组间质浸润≥1/2的比例低于化疗组[53%(46/86)比73%(35/48),P = 0.027],淋巴结转移比例显著低于照射组[17%(15/86)比29%(26/90),P = 0.046],无危险因素率显著高于化疗组[44%(38/86)比25%(12/48),P = 0.028]。化疗联合照射组、化疗组和照射组术后放疗比例分别为47%(40/86)、67%(32/48)和62%(56/90),差异有统计学意义(P = 0.035)。5年无病生存率(DFS)分别为79%、75%和78%。3组5年总生存率(OS)分别为81%、78%和81%,差异无统计学意义(P>0.05)。224例患者中,术后有0、1和≥2个危险因素患者的5年DFS分别为90%、75%和57%,OS分别为95%、82%和65%,差异无统计学意义(P均<0.01)。术后无危险因素患者中,未接受术后放疗患者的5年OS为96%,接受术后放疗患者为89%,差异无统计学意义(P = 0.263)。
Ib2期和IIa2期患者中,新辅助化疗联合阴道腔内照射组、单纯新辅助化疗组和单纯阴道腔内照射组的DFS和OS无差异。新辅助治疗后无危险因素的患者预后较好。