Çakır Caner, Kılıç Fatih, Dur Rıza, Yüksel Dilek, Ünsal Mehmet, Korkmaz Vakkas, Kılıç Çiğdem, Kimyon Cömert Günsu, Boran Nurettin, Türkmen Osman, Koç Sevgi, Turan Taner
Etlik Zübeyde Hanım Women's Health Training and Research Hospital, Clinic of Obstetrics and Gynecology, Ankara, Turkey
Turk J Obstet Gynecol. 2021 Sep 27;18(3):190-202. doi: 10.4274/tjod.galenos.2021.70493.
This study aimed to evaluate neoadjuvant chemotherapy (NACT) for locally advanced stage cervical carcinoma.
Data of 43 patients with locally advanced cervical carcinoma who had NACT were reviewed. NACT protocols implemented included cisplatin/5-fluorauracil, cisplatin/UFT, and carboplatin/paclitaxel. After NACT, the patients were re-examined, and patients who had a tumor size ≤40 mm underwent Piver-Rutledge type III radical hysterectomy, while other patients received radiotherapy. Following NACT, clinical responses were assessed according to the criteria of the World Health Organization.
The mean age of the patients was 49.4 years, and the median follow-up duration was 48 (range, 5-228) months. The median tumor sizes were 50 and 30 mm before and after NACT, respectively. Complete clinical response was observed in 4 (9.3%) patients, partial clinical response in 8 (18.6%), and pathologic complete response in 3 (6.9%). Stable disease was noted in 30 (69.9%) patients and progression in 1 (2.3%) patient. After NACT, 31 patients have undergone radical surgical procedures. The 5-year disease-free survival rate was 72%, and the 5-year disease-specific survival rate was 91%. Age, International Federation of Gynaecology and Obstetrics 2009 stage, histopathologic type, NACT protocol, rate of decrease in tumor size after NACT, clinical response, number of courses, tumor size before NACT, tumor size after NACT, and lymph node metastasis were not associated with disease-free survival.
Following NACT, a significant reduction in tumor dimension was observed, and the probability of radical surgery is increased. However, clinical response was not predictive of survival.
本研究旨在评估新辅助化疗(NACT)用于局部晚期宫颈癌的效果。
回顾了43例接受NACT的局部晚期宫颈癌患者的数据。实施的NACT方案包括顺铂/5-氟尿嘧啶、顺铂/优福定以及卡铂/紫杉醇。NACT后,对患者进行复查,肿瘤大小≤40 mm的患者接受Piver-Rutledge III型根治性子宫切除术,其他患者接受放疗。NACT后,根据世界卫生组织的标准评估临床反应。
患者的平均年龄为49.4岁,中位随访时间为48(范围5 - 228)个月。NACT前后的中位肿瘤大小分别为50 mm和30 mm。4例(9.3%)患者观察到完全临床缓解,8例(18.6%)为部分临床缓解,3例(6.9%)为病理完全缓解。30例(69.9%)患者疾病稳定,1例(2.3%)患者病情进展。NACT后,31例患者接受了根治性手术。5年无病生存率为72%,5年疾病特异性生存率为91%。年龄、国际妇产科联盟2009分期、组织病理类型、NACT方案、NACT后肿瘤大小减小率、临床反应、疗程数、NACT前肿瘤大小、NACT后肿瘤大小以及淋巴结转移与无病生存均无关。
NACT后,观察到肿瘤尺寸显著减小,根治性手术的可能性增加。然而,临床反应并不能预测生存情况。