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在输卵管中发现偶然的p53特征后的临床结果。

Clinical outcomes following identification of an incidental p53 signature in the fallopian tube.

作者信息

MacARTHUR Emily C, Radolec Mackenzy, Rinda Soong T, Elishaev Esther, Buckanovich Ronald, Taylor Sarah E, Lesnock Jamie

机构信息

Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Hospital of UPMC, Pittsburgh, PA, United States.

Division of Gynecologic Oncology, Magee-Womens Hospital of UPMC, Pittsburgh, PA, United States.

出版信息

Gynecol Oncol Rep. 2024 Mar 5;52:101359. doi: 10.1016/j.gore.2024.101359. eCollection 2024 Apr.

Abstract

Fallopian tube pathology in patients with and mutations suggests a possible pathway to high grade serous ovarian carcinoma originates with a p53 signature, which is thought to represent a potential precursor to serous tubal intraepithelial carcinoma (STIC). The clinical implications of an isolated p53 signature in the average-risk population has not been well-established. This study aims to describe clinical outcomes in patients with incidentally noted p53 signature lesions. All patients diagnosed with a p53 signature lesion on final pathology from 2014 to 2022 were identified at a large academic institution. P53 signature is defined by our lab as morphologically normal to mildly atypical tubal epithelium with focal p53 over-expression on immunohistochemistry. Incidental p53 signature was defined as identification of a fallopian tube lesion excised for benign or unrelated indications in patients without a known hereditary disposition. Demographic, clinicopathologic, and genetic data were collected. A total of 127 patients with p53 signatures were identified. Thirty-six patients were excluded for established ovarian cancer or high-risk history leaving 91 total patients. Five patients (5.5%) developed a malignancy, none of which were ovarian or primary peritoneal, at the end of the eight and a half year follow up period. Twenty-four (26.4%) patients had salpingectomy without any form of oophorectomy at the time of initial surgery, while 67 (73.6%) patients had at least a unilateral oophorectomy at the time of their salpingectomy. Seven patients (7.7%) had additional surgery after p53 signature diagnosis; however, the final pathology yielded no evidence of malignancy in all these patients. After subsequent surgeries, 19 (20.9%) patients maintained their ovaries. The diagnosis of an incidental p53 signature was not associated with any primary peritoneal or ovarian cancer diagnoses during our follow up, and the majority of patients were managed conservatively by their providers with no further intervention after diagnosis.

摘要

携带BRCA1和BRCA2突变的患者的输卵管病理学表明,高级别浆液性卵巢癌可能起源于一种p53特征性病变,这种病变被认为是浆液性输卵管上皮内癌(STIC)的潜在前体。在一般风险人群中,孤立的p53特征性病变的临床意义尚未完全明确。本研究旨在描述偶然发现p53特征性病变的患者的临床结局。在一家大型学术机构中,确定了所有在2014年至2022年最终病理检查中诊断为p53特征性病变的患者。我们实验室将p53特征性病变定义为形态学上正常至轻度不典型的输卵管上皮,免疫组化显示局灶性p53过表达。偶然的p53特征性病变定义为在无已知遗传倾向的患者中,因良性或无关指征切除的输卵管病变。收集了人口统计学、临床病理和基因数据。共确定了127例具有p53特征性病变的患者。36例因已确诊卵巢癌或有高危病史被排除,最终共有91例患者。在八年半的随访期结束时,5例患者(5.5%)发生了恶性肿瘤,但均不是卵巢或原发性腹膜恶性肿瘤。24例(26.4%)患者在初次手术时进行了输卵管切除术,未进行任何形式的卵巢切除术,而67例(73.6%)患者在进行输卵管切除术时至少进行了单侧卵巢切除术。7例(7.7%)患者在诊断为p53特征性病变后进行了额外手术;然而,所有这些患者的最终病理检查均未发现恶性肿瘤证据。在随后的手术中,19例(20.9%)患者保留了卵巢。在我们的随访期间,偶然的p53特征性病变诊断与任何原发性腹膜或卵巢癌诊断均无关联,大多数患者由其医疗服务提供者进行保守管理,诊断后未进行进一步干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748d/10943111/ab1def0574d0/gr1.jpg

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