Evidence for Diverse Prognosis in High-Grade Serous Ovarian Carcinoma: Solid, Pseudoendometrioid, and Transitional-Like; So-Called "SET Morphology" and Progesterone Receptor Status.

IF 1.1 Q4 PATHOLOGY
Halit Uner, Metin Demir, Dincer Goksuluk, Ayse Kars, Meral Uner, Alp Usubutun
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引用次数: 1

Abstract

Objective: High-grade serous ovarian carcinoma (HGSC) is one of the major tumors of the gynecological system with a poor survival rate and variable microscopic appearance. It was suggested that SET (solid, pseudo-endometrioid and transitional-like) morphology in ovarian HGSC is predictably associated with BRCA deficiencies. In this study, we investigated the microscopic patterns and some immunohistochemical markers predicting the prognosis of serous carcinoma.

Material and method: We re-evaluated 305 HGSC ovarian resections morphologically and calculated the SET morphology percentages for each case. Morphological and immunohistochemical data correlated with the survival and post-treatment disease progression data.

Results: The median age at diagnosis was 57 years and the median follow-up period was 3.1 years. The median overall survival (OS) of ovarian carcinoma in SET-predominant tumors (n=60) was 81 months, while for tumors with SET non-dominant morphology (n=63) and non-SET morphology (n=182) it was 59.7 and 44.7 months, respectively.

Conclusion: Predominant (more than 50%) SET morphology was significantly associated with increased survival rates of HGSC. Immunohistochemically, p53, ERCC1, ER, and PR antibodies were applied and only PR antibody positivity was found to be associated with borderline statistical significance for increased survival rates. Our results suggest that SET morphology may be a potential predictive and prognostic marker in managing the treatment strategies of HGSC.

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高级别浆液性卵巢癌不同预后的证据:实体癌、假子宫内膜样癌和移行样癌;所谓的“SET形态学”和孕酮受体状态。
目的:高级别浆液性卵巢癌(HGSC)是妇科系统的主要肿瘤之一,生存率低,镜下表现多变。有人认为,卵巢HGSC中的SET(实体、假子宫内膜样和移行样)形态可预测地与BRCA缺陷相关。在这项研究中,我们研究了浆液性癌的显微镜模式和一些免疫组织化学标志物预测预后。材料和方法:我们从形态学角度重新评估了305例HGSC卵巢切除术,并计算了每个病例的SET形态学百分比。形态学和免疫组织化学数据与生存率和治疗后疾病进展数据相关。结果:诊断时的中位年龄为57岁,中位随访期为3.1年。SET占优势的肿瘤(n=60)的卵巢癌的中位总生存期(OS)为81个月,而SET非占优势形态(n=63)和非SET形态(n=182)的肿瘤分别为59.7和44.7个月。结论:占优势(50%以上)的SET形态与HGSC生存率的提高显著相关。免疫组化显示,应用p53、ERCC1、ER和PR抗体,发现只有PR抗体阳性与生存率增加的临界统计学意义相关。我们的研究结果表明,SET形态可能是管理HGSC治疗策略的潜在预测和预后标志物。
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来源期刊
CiteScore
1.90
自引率
10.00%
发文量
23
审稿时长
14 weeks
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