Mossa B, Mossa S, Corosu L, Marziani R
Department of Gynecology, Perinatology and Child-Health, University of Rome "Sapienza" Division of Gynecology, Sant'Andrea Hospital, Rome, Italy.
Eur J Gynaecol Oncol. 2010;31(5):497-503.
To assess the role of neoadjuvant chemotherapy to achieve radical surgery in a larger number of patients with locally advanced/or bulky Stage IB cervical carcinoma. We conducted a trial to determine whether neoadjuvant chemotherapy would improve disease-free survival and overall survival in Stage IB-III cervical cancer.
Prospective randomized clinical study with long-term follow-up.
Department of Gynecology, Perinatology and Child Health, II Faculty University of Rome "La Sapienza".
288 patients with squamous cell carcinoma of the uterine cervix, FIGO Stage IB-IIIB were randomized to one of the following treatments: three courses of neoadjuvant chemotherapy with cisplatin, vincristine, bleomycin (NACT arm; n = 159); conventional surgery or exclusive radiotherapy (CONV arm; n = 129). There was no difference in age, FIGO stage, tumor size and lymph node involvement between the two groups (p = ns). Two hundred and thirty-four patients in Stage IB-IIb (n = 129 NACT arm and n = 105 CONV arm) and 24 patients in Stage III (NACT arm) who proved to be chemosensitive underwent radical hysterectomy. Six Stage III patients, non responders to chemotherapy, and 24 patients, Stage III of the CONV arm, underwent radiotherapy. Follow-up extended for seven years.
The study was performed on disease-free survival related to several prognostic factors: age, FIGO stage, tumor size, grading, parametrial involvement, lymph node status and surgical margins. Recurrence of disease occurred in 49 (32.1%) patients of the NACT arm (n = 153) and in 39 (37.1%). patients of the CONV arm (n = 105). Statistically significant differences in the recurrence of the disease were related to FIGO stage (p < 003), grading (p < .05), parametrial involvement (p < .002) lymph node status (p < .0001) and tumor size (p <.002). No statistical significance was related to age and surgical margins (p = ns). Disease-free and overall survival in the two groups were, respectively, 65.4% vs 53.5% (p = ns) and 70.4% 65.9% (p = ns).
评估新辅助化疗在使更多局部晚期/体积较大的IB期宫颈癌患者实现根治性手术方面的作用。我们开展了一项试验,以确定新辅助化疗是否会改善IB - III期宫颈癌患者的无病生存期和总生存期。
长期随访的前瞻性随机临床研究。
罗马第二大学“La Sapienza”妇产科、围产医学与儿童健康系。
288例子宫颈鳞状细胞癌患者,国际妇产科联盟(FIGO)分期为IB - IIIB期,被随机分为以下治疗组之一:接受三疗程顺铂、长春新碱、博来霉素新辅助化疗(新辅助化疗组;n = 159);传统手术或单纯放疗(传统治疗组;n = 129)。两组在年龄、FIGO分期、肿瘤大小和淋巴结受累情况方面无差异(p =无统计学意义)。IB - IIb期的234例患者(新辅助化疗组n = 129例,传统治疗组n = 105例)以及III期的24例对化疗敏感的患者(新辅助化疗组)接受了根治性子宫切除术。6例III期化疗无反应患者以及传统治疗组的24例III期患者接受了放疗。随访长达七年。
该研究针对与多个预后因素相关的无病生存期进行:年龄、FIGO分期、肿瘤大小、分级、宫旁组织受累情况、淋巴结状态和手术切缘。新辅助化疗组(n = 153)的49例(32.1%)患者和传统治疗组(n = 105)的39例(37.1%)患者出现疾病复发。疾病复发的统计学显著差异与FIGO分期(p < 0.03)、分级(p < 0.05)、宫旁组织受累情况(p < 0.002)、淋巴结状态(p < 0.0001)和肿瘤大小(p < 0.002)有关。与年龄和手术切缘无关(p =无统计学意义)。两组的无病生存期和总生存期分别为65.4%对53.5%(p =无统计学意义)和70.4%对65.9%(p =无统计学意义)。