Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, CA, USA.
Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA, USA.
Ann Surg Oncol. 2021 Mar;28(3):1740-1748. doi: 10.1245/s10434-020-09202-1. Epub 2020 Oct 15.
This study was designed to examine the association between malignant peritoneal cytology and survival of women with uterine sarcoma.
This retrospective, observational study queried the National Cancer Institute's Surveillance, Epidemiology, and End Result Program. Uterine sarcoma cases diagnosed from 2010 to 2016 with known peritoneal cytology results were examined. Propensity score inverse probability of treatment weighting was fitted to balance the measured covariates. Overall survival (OS) was compared between malignant and negative cytology cases.
A total of 1481 uterine sarcomas were examined. Malignant peritoneal cytology was seen in 146 (9.9%) cases. Women who had T3 disease and distant metastases had the highest incidence of malignant peritoneal cytology (43.1%). In multivariable analysis, higher T stage, nodal involvement, distant metastasis, poorer tumor differentiation, and rhabdomyosarcoma/endometrial stromal sarcoma were significantly associated with an increased risk of malignant peritoneal cytology (all, P < 0.05). In the weighted model, malignant peritoneal cytology was associated with a nearly twofold increased risk of all-cause mortality compared with negative peritoneal cytology (3-year OS rate 34.7% versus 60.2%; hazard ratio 2.26; 95% confidence interval 1.88-2.71; P < 0.001). The absolute difference in the 3-year survival rate was particularly large in leiomyosarcoma (3-year OS rate 2.8% versus 51.9%; hazard ratio 2.64; 95% confidence interval 1.94-3.59; P < 0.001). Malignant peritoneal cytology was also associated with an increased all-cause mortality risk in early and advanced stages (both, P < 0.05).
Our study suggests that malignant peritoneal cytology may be a prognostic factor for increased mortality in uterine sarcoma, particularly in uterine leiomyosarcoma.
本研究旨在探讨恶性腹腔细胞学与子宫肉瘤患者生存的关系。
本回顾性观察性研究查询了美国国家癌症研究所的监测、流行病学和最终结果计划。检查了 2010 年至 2016 年期间已知腹腔细胞学结果的子宫肉瘤病例。采用倾向评分逆概率治疗加权法平衡了测量的协变量。比较了恶性和阴性细胞学病例的总生存率(OS)。
共检查了 1481 例子宫肉瘤。146 例(9.9%)发现恶性腹腔细胞学。患有 T3 疾病和远处转移的女性恶性腹腔细胞学发生率最高(43.1%)。多变量分析显示,较高的 T 分期、淋巴结受累、远处转移、较差的肿瘤分化以及横纹肌肉瘤/子宫内膜间质肉瘤与恶性腹腔细胞学的风险增加显著相关(均 P<0.05)。在加权模型中,与阴性腹腔细胞学相比,恶性腹腔细胞学与全因死亡率增加近两倍相关(3 年 OS 率 34.7%对 60.2%;危险比 2.26;95%置信区间 1.88-2.71;P<0.001)。在平滑肌肉瘤中,3 年生存率的绝对差异尤其大(3 年 OS 率 2.8%对 51.9%;危险比 2.64;95%置信区间 1.94-3.59;P<0.001)。恶性腹腔细胞学也与早期和晚期的全因死亡率增加风险相关(均 P<0.05)。
我们的研究表明,恶性腹腔细胞学可能是子宫肉瘤死亡风险增加的预后因素,特别是在子宫平滑肌肉瘤中。