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子宫平滑肌肉瘤的临床结局和预后标志物:一项基于人群的队列研究

Clinical outcomes and prognostic markers in uterine leiomyosarcoma: a population-based cohort.

作者信息

Garcia Christine, Kubat Jenna S, Fulton Regan S, Anthony Adam T, Combs Mary, Powell C Bethan, Littell Ramey D

机构信息

*Division of Gynecologic Oncology, and †Department of Pathology, The Permanente Medical Group, San Francisco, CA; and ‡Division of Biostatistics, University of California, Berkeley, CA.

出版信息

Int J Gynecol Cancer. 2015 May;25(4):622-8. doi: 10.1097/IGC.0000000000000370.

Abstract

OBJECTIVE

The aim was to identify clinical parameters and immunohistochemical markers predictive of recurrence and overall survival (OS) in a community cohort of patients with primary uterine leiomyosarcoma (ULMS).

METHODS/MATERIALS: All patients with new diagnosis of ULMS from 1999 to 2007 were identified from the Kaiser Permanente Northern California pathology database. A retrospective chart review was performed to gather demographic and clinical data. The primary outcomes were recurrence-free survival and OS. In addition, a subset of tumor samples was available to analyze 3 immunohistochemical markers using tissue microarray techniques; these are as follows: estrogen receptor (ER) alpha, epidermal growth factor receptor (EGFR), and Ki-67.

RESULTS

Seventy-five patients with ULMS were identified, of which 63 had adequate tumor tissue available for immunohistochemical evaluation. The median follow-up for all stages was 28 months. The rate of recurrence or progressive disease was 76% for stage I patients compared with 85% for stage II to IV patients. At 3 years, 37% of stage I patients were recurrence free compared with 27% of stage II to IV patients. Overall survival for stage I patients declined from 64% to 38% between 3 and 5 years while remaining stable at 30% for stage II to IV patients. In multivariable analysis, increasing mitotic counts were associated with increased risk of recurrence (hazards ratio [HR], 3.2; P = 0.013) and a trend toward decreased OS (HR, 2.2; P = 0.10). Expression of ER (HR, 1.0), EGFR expression (HR, 1.0), and Ki-67 expression (HR, 1.0) were not predictive of recurrence or OS.

CONCLUSIONS

Recurrence rate of 76% for patients with stage I ULMS was higher than previously published cohorts. Mitotic counts were associated with increased recurrence and decreased OS. Expressions of ER, EGFR, and Ki-67 were not useful for predicting overall recurrence or survival.

摘要

目的

旨在确定原发性子宫平滑肌肉瘤(ULMS)患者社区队列中预测复发和总生存期(OS)的临床参数及免疫组化标志物。

方法/材料:从北加利福尼亚凯撒医疗集团病理数据库中识别出1999年至2007年所有新诊断为ULMS的患者。进行回顾性病历审查以收集人口统计学和临床数据。主要结局为无复发生存期和总生存期。此外,利用组织芯片技术对一部分肿瘤样本进行分析,以检测三种免疫组化标志物,具体如下:雌激素受体(ER)α、表皮生长因子受体(EGFR)和Ki-67。

结果

共识别出75例ULMS患者,其中63例有足够的肿瘤组织可用于免疫组化评估。所有分期患者的中位随访时间为28个月。I期患者的复发或疾病进展率为76%,而II至IV期患者为85%。3年时,I期患者37%无复发,II至IV期患者为27%。I期患者的总生存期在3至5年间从64%降至38%,而II至IV期患者则稳定在30%。多变量分析显示,有丝分裂计数增加与复发风险增加相关(风险比[HR],3.2;P = 0.013),且有总生存期降低的趋势(HR,2.2;P = 0.10)。ER表达(HR,1.0)、EGFR表达(HR,1.0)和Ki-67表达(HR,1.0)均不能预测复发或总生存期。

结论

I期ULMS患者76%的复发率高于先前发表的队列。有丝分裂计数与复发增加和总生存期降低相关。ER、EGFR和Ki-67的表达对预测总体复发或生存期并无帮助。

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