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Clinicopathologic parameters and immunohistochemical study of endometrial stromal sarcomas
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Clinicopathologic parameters and immunohistochemical study of endometrial stromal sarcomas

Tzu-I. Wu, Hung-Hsueh Chou, Chi-Ju Yeh, Swei Hsueh, Jung-Erh Yang, Mei-Shan Jao, Ting-Chang Chang, Chun-Sen Hsu, Kwang-Huei LinChyong-Huey Lai
International Journal of Gynecological Pathology, 卷.32(5), 頁碼.482-492
09/2013
PMID: 23896713

摘要

Endometrial stromal sarcoma Immunohistochemistry Prognostic factors Survival Pathology and Forensic Medicine Obstetrics and Gynecology
We aimed to investigate the clinicopathologic features, immunohistochemical studies, and prognosis in patients with endometrial stromal sarcoma (ESS). Clinical information was reviewed retrospectively for cases of ESS (1985-2009). A histologic review and immunohistochemical staining for the estrogen receptor, progesterone receptor, c-Kit, CD-10, Ki-67, and m-TOR were performed. Sixty-one patients (median age, 44 y; range, 22-71) were eligible for analysis (1988 International Federation of Gynecology and Obstetrics Stage I, 43; Stage II, 2; Stage III, 11; Sage IV, 4; unstaged, 1). The median follow-up period for survivors was 73 mo. Of those, the patients who underwent an adnexectomy and a pelvic lymphadenectomy, 15% and 13%, respectively, revealed metastasis. There were 20 relapses/persistence, including 13 (65%) in the pelvis and abdomen and 7 (35%) in distant sites. Eight patients died from ESS at a median duration of 14.5 mo (range, 2-50 mo) after relapse. Five- and 10-yr cancer-specific survival (CSS) rates were 88% and 85%, respectively; and 5- and 10-yr progression-free survival rates were 69% and 57%, respectively. Stage, residual disease, and high proliferative index of Ki-67 were significant prognostic factors for both progression-free survival and CSS in a univariate analysis, in addition to mitotic index for CSS. Multivariate analysis selected only residual disease as an independent variable for progression-free survival and stage and residual disease for CSS. Our results support using clinical Stage I, no residual disease, low proliferative index of Ki-67, and estrogen receptor/progesterone receptor overexpression as potential biomarkers to select patients with ESS for fertility-preservation surgery (5 such patients were alive and free). © 2013 International Society of Gynecological Pathologists.

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