Endometrial cancer arising in adenomyosis versus endometrial cancer coexisting with adenomyosis: are these two different entities?

被引:41
作者
Machida, Hiroko [1 ]
Maeda, Midori [4 ]
Cahoon, Sigita S. [1 ]
Scannell, Christopher A. [3 ]
Garcia-Sayre, Jocelyn [1 ]
Roman, Lynda D. [1 ,2 ]
Matsuo, Koji [1 ,2 ]
机构
[1] Univ Southern Calif, Los Angeles Cty Med Ctr, Div Gynecol Oncol, Dept Obstet & Gynecol, 2020 Zonal Ave,IRD 520, Los Angeles, CA 90089 USA
[2] Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[3] Univ Southern Calif, Keck Sch Med, Los Angeles, CA USA
[4] Natl Ctr Global Hlth & Med, Tokyo, Japan
关键词
Endometrial cancer; Adenomyosis; Endometriosis--associated cancer; Survival; Prognosis; EPITHELIAL OVARIAN-CANCER; CLEAR-CELL ADENOCARCINOMA; IMMUNOHISTOCHEMICAL ANALYSIS; MALIGNANT-TRANSFORMATION; INVASIVE ADENOCARCINOMA; UTERINE ADENOMYOSIS; CYSTIC ADENOMYOSIS; TUMOR PROGRESSION; CARCINOMA; EXPRESSION;
D O I
10.1007/s00404-017-4375-z
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
While adenomyosis is one of the most common benign histologic findings in hysterectomy specimens of endometrial cancer, demographics of endometrial cancer arising in adenomyosis (EC-AIA) has not been well elucidated. The aim of this study is to evaluate histopathological findings and disease-free survival (DFS) of EC-AIA in comparison to endometrial cancer coexisting with adenomyosis (EC-A). EC-AIA cases were identified via a systematic literature search (n = 46). EC-A cases were identified from a historical cohort that underwent hysterectomy-based surgical staging in two institutions (n = 350). Statistical comparisons of the two groups were based on univariate and multivariate analyses. The EC-AIA group was significantly older than the EC-A group (58.9 versus 53.8, p = 0.002). As to tumor characteristics, 63.6% of EC-AIA cases reported tumor within the myometrium without endometrial extension. The EC-AIA group was significantly associated with more non-endometrioid histology (23.9 versus 14.8%; p = 0.002) and deep myometrial tumor invasion (51.6 versus 19.4%; p < 0.001) than EC-A. Tumor grade, stage, and nodal metastasis risk were similar (all, p > 0.05). In a univariate analysis, the EC-AIA group had a significantly decreased DFS compared to EC-A (5-year rates, 72.2 versus 85.5%, p = 0.001). After controlling for age, histology, tumor grade, and stage, EC-AIA remained an independent prognostic factor associated with decreased DFS compared to EC-A (adjusted-hazard ratio 2.87, 95% confidence interval 1.44-5.70, p = 0.031). Our study demonstrated that EC-AIA has distinct tumor characteristics and a poorer survival outcome compared to EC-A. This suggests a benefit of recognition of this unique entity as an aggressive variant of endometrial cancer.
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收藏
页码:1459 / 1468
页数:10
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