Grasso Silvana, Loizzi Vera, Minicucci Valentina, Resta Leonardo, Camporeale Anna Lina, Cicinelli Ettore, Cormio Gennaro
Department of Biomedical Science and Human Oncology, Obstetrics and Gynecology Unit, University of Bari, Bari, Italy.
Oncology. 2017;92(4):197-204. doi: 10.1159/000452277. Epub 2017 Jan 17.
The aim of our study was to evaluate the clinicopathological features and prognostic factors of uterine carcinosarcoma.
In this retrospective study, the clinical characteristics of 44 patients with uterine MMMT were evaluated. Survival curves were estimated by the Kaplan-Meier method and compared by the log-rank test.
Forty-four patients with uterine carcinosarcoma were referred to our unit between 1995 and 2015. Their median age was 66.5 years. All women underwent total abdominal hysterectomy and bilateral salpingo-oophorectomy. Twenty-five percent had omental resection. Pelvic lymphadenectomy was performed in 18.2% of the cases. Twenty-six of the patients presented with stage I/II disease, 17 with advanced stages. In 20.5% of the cases there were metastases at diagnosis. Forty women received adjuvant chemotherapy, with complete remission in 67.9% of the cases. Recurrences were observed in 27.3% of the women. Disease-free and overall survival was 27 and 103 months, respectively. The FIGO stage, histological type, tumour size, chemotherapy regimen, pelvic lymphadenectomy, and myometrial invasion did not affect survival.
Uterine MMMT is an aggressive tumour, often diagnosed at an advanced stage and with a high rate of metastases or recurrences. Because of its rarity, its management is controversial and fixed prognostic factors cannot be defined.
本研究旨在评估子宫癌肉瘤的临床病理特征及预后因素。
在这项回顾性研究中,对44例子宫恶性中胚叶混合瘤患者的临床特征进行了评估。采用Kaplan-Meier法估计生存曲线,并通过对数秩检验进行比较。
1995年至2015年间,44例子宫癌肉瘤患者转诊至我科。她们的中位年龄为66.5岁。所有女性均接受了全腹子宫切除术及双侧输卵管卵巢切除术。25%的患者进行了大网膜切除术。18.2%的病例进行了盆腔淋巴结清扫术。26例患者为Ⅰ/Ⅱ期疾病,17例为晚期。20.5%的病例在诊断时有转移。40例患者接受了辅助化疗,67.9%的病例完全缓解。27.3%的女性出现复发。无病生存期和总生存期分别为27个月和103个月。国际妇产科联盟(FIGO)分期、组织学类型、肿瘤大小、化疗方案、盆腔淋巴结清扫术及肌层浸润均不影响生存。
子宫恶性中胚叶混合瘤是一种侵袭性肿瘤,常于晚期诊断,转移率或复发率高。由于其罕见性,其治疗存在争议,无法确定固定的预后因素。