原发性卵巢平滑肌肉瘤的综合基因组分析和临床病理特征。

IF 4.7 2区 医学 Q1 OBSTETRICS & GYNECOLOGY
Matteo Bruno, Elisa De Paolis, Angelo Minucci, Alessia Piermattei, Giulia Maneri, Angela Santoro, GianFranco Zannoni, Giovanni Scambia, Carolina Maria Sassu, Francesca Ciccarone, Camilla Nero, Claudia Marchetti, Anna Fagotti
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引用次数: 0

摘要

目的:原发性卵巢平滑肌肉瘤极为罕见,占卵巢恶性肿瘤的不到0.1%。他们的治疗策略仍然不明确,缺乏全面的基因组分析数据。本研究旨在描述原发性卵巢平滑肌肉瘤的病理特征和基因组图谱,并根据现有文献强调其与子宫平滑肌肉瘤的相似性。方法:回顾性分析2013年至2023年在三级转诊中心诊断的7例组织学证实的原发性卵巢平滑肌肉瘤病例。我们回顾了临床资料、组织病理学结果和免疫组织化学特征。使用TruSight Oncology 500检测进行基因组分析,针对523个癌症相关基因。仅考虑致癌或可能致癌的改变(分级系统I-II)。结果:所有患者均为国际妇产科联合会IA期疾病,均行根治性手术。2例出现盆腔复发;复发肿瘤均显示Ki-67升高,雌激素和孕激素受体完全丧失。组织学上,肿瘤呈梭形或上皮样形态,具有不同的异型性和有丝分裂指数。基因组分析显示TP53(71%)和PTEN(57%)改变的患病率很高。在同源重组修复基因(BRCA2、CHEK1/2和ATM)、成纤维细胞生长因子(FGF)家族成员(FGF7/9/14)和血小板源性生长因子受体β中发现了额外的拷贝数改变。所有病例的肿瘤突变负荷均为中低,微卫星状态稳定。结论:原发性卵巢平滑肌肉瘤表现出复杂的基因组景观,其特征是基因组不稳定,与子宫平滑肌肉瘤具有相同的关键改变。TP53和PTEN突变可能在其发病机制中起核心作用。这是卵巢平滑肌肉瘤的首次基因组图谱分析,为进一步研究和这种罕见恶性肿瘤的潜在靶向治疗提供了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive genomic profiling and clinico-pathologic characterization of primary ovarian leiomyosarcoma.

Objective: Primary ovarian leiomyosarcomas are exceptionally rare, accounting for less than 0.1% of ovarian malignancies. Their treatment strategies remain poorly defined, and data on comprehensive genomic profiling are lacking. This study aims to characterize the pathological features and genomic landscape of primary ovarian leiomyosarcoma, highlighting similarities with uterine leiomyosarcomas based on available literature.

Methods: We retrospectively analyzed 7 histologically confirmed cases of primary ovarian leiomyosarcoma diagnosed between 2013 and 2023 at a tertiary referral center. Clinical data, histopathological findings, and immunohistochemical profiles were reviewed. Genomic profiling was performed using the TruSight Oncology 500 assay, targeting 523 cancer-related genes. Only oncogenic or likely oncogenic alterations (Tier classification system I-II) were considered.

Results: All patients had International Federation of Gynecology and Obstetrics stage IA disease and underwent radical surgery. Two patients experienced pelvic recurrence; both showed increased Ki-67 and complete loss of estrogen and progesterone receptors in the relapsed tumors. Histologically, tumors exhibited spindle or epithelioid morphology with variable atypia and mitotic indices. Genomic profiling revealed a high prevalence of TP53 (71%) and PTEN (57%) alterations. Additional copy number alterations were identified in homologous recombination repair genes (BRCA2, CHEK1/2, and ATM), fibroblast growth factor (FGF) family members (FGF7/9/14), and platelet-derived growth factor receptor beta. Tumor mutational burden was low to medium in all cases, and microsatellite status was stable.

Conclusions: Primary ovarian leiomyosarcomas exhibit a complex genomic landscape marked by genomic instability, sharing key alterations with uterine leiomyosarcomas. TP53 and PTEN mutations may play a central role in their pathogenesis. This first genomic profiling analysis of ovarian leiomyosarcomas provides a basis for further research and potential targeted therapeutic approaches in this rare malignancy.

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来源期刊
CiteScore
6.60
自引率
10.40%
发文量
280
审稿时长
3-6 weeks
期刊介绍: The International Journal of Gynecological Cancer, the official journal of the International Gynecologic Cancer Society and the European Society of Gynaecological Oncology, is the primary educational and informational publication for topics relevant to detection, prevention, diagnosis, and treatment of gynecologic malignancies. IJGC emphasizes a multidisciplinary approach, and includes original research, reviews, and video articles. The audience consists of gynecologists, medical oncologists, radiation oncologists, radiologists, pathologists, and research scientists with a special interest in gynecological oncology.
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