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高危原发性前列腺外胃肠道间质瘤的全外显子组测序:一例报告

Whole-exome sequencing for high-risk primary prostatic extra-gastrointestinal stromal tumor: A case report.

作者信息

Lu Li, Qu Hu, Wang De Juan, Yao Bin, Ma Bo, Qiu Jian Guang, Wang Zhong Yang, Ren Dong Lin

机构信息

Department of Rectal Surgery, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangdong Institute of Gastroenterology, Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangzhou, Guangdong 510655, P.R. China.

Department of Urology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangdong Institute of Gastroenterology, Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Guangzhou, Guangdong 510655, P.R. China.

出版信息

Mol Clin Oncol. 2021 Dec;15(6):249. doi: 10.3892/mco.2021.2411. Epub 2021 Oct 1.

Abstract

The low incidence rates of prostatic extra-gastrointestinal stromal tumors (EGIST), combined with the lack of published guidelines on its treatment, often results in its misdiagnosis and challenges in the treatment of patients, even in cases with high-risk factors. The present case study reported a 65-years-old Chinese male patient, who presented with intermittent hematuria and lower urinary tract symptoms for three months. The colonoscopy results revealed no gastrointestinal lesions; however, a core biopsy diagnosed an EGIST, which subsequently underwent radical prostatocystotomy, standard pelvic lymph node resection, and bricker ileal conduit diversion. The postoperative pathological results suggested a high-risk primary prostatic EGIST, according to the aggressive behavior of the GIST. The immunohistochemistry results revealed the positive expression of CD117, DOG1, CD34, androgen receptor AR, prostate-specific antigen (PSA), a 2% Ki-67 index and a positive surgical margin. The whole exome sequencing (WES) results revealed that the patient harbored a single nucleotide mutation in 121 genes and copy number variations in 601 genes, including a defect in c-Kit (in-frame deletion in p.Q556-V560; fold, 17.5%). By compiling the data obtained from the ConsensusPathDB and the drug-gene interaction databases and expert opinions, the patient was prescribed with the personalized drugs (400 mg per day imatinib mesylate and 50 mg per day bicalutamide, which were stopped when the PSA levels remained stable below 0.01 ng/ml) for 18 months follow-up and there were no signs of recurrence. In conclusion, WES identified multiple genomic alterations and the underlying genetic defect in the rare case enabled the evaluation of the prognosis and the decision of potential drug candidates. The underlying mechanism of the substantial genetic variations in the primary prostatic EGIST, as well as the malignant behaviors of the tumor, remain to be investigated.

摘要

前列腺外胃肠道间质瘤(EGIST)发病率低,加上缺乏关于其治疗的已发表指南,常常导致误诊以及患者治疗面临挑战,即便在存在高危因素的病例中也是如此。本病例研究报告了一名65岁的中国男性患者,他出现间歇性血尿和下尿路症状达三个月。结肠镜检查结果显示无胃肠道病变;然而,一次穿刺活检诊断为EGIST,随后该患者接受了根治性前列腺膀胱切除术、标准盆腔淋巴结清扫术以及回肠代膀胱术。术后病理结果根据GIST的侵袭性行为提示为高危原发性前列腺EGIST。免疫组化结果显示CD117、DOG1、CD34、雄激素受体AR、前列腺特异性抗原(PSA)呈阳性表达,Ki-67指数为2%,手术切缘阳性。全外显子测序(WES)结果显示该患者在121个基因中存在单核苷酸突变,在601个基因中存在拷贝数变异,包括c-Kit缺陷(p.Q556-V560框内缺失;倍数,17.5%)。通过汇总从ConsensusPathDB和药物-基因相互作用数据库获得的数据以及专家意见,为该患者开具了个性化药物(每天400毫克甲磺酸伊马替尼和每天50毫克比卡鲁胺,当PSA水平稳定在0.01纳克/毫升以下时停药),进行了18个月的随访,没有复发迹象。总之,WES识别出多种基因组改变,这例罕见病例中的潜在基因缺陷有助于评估预后并决定潜在的候选药物。原发性前列腺EGIST中大量基因变异的潜在机制以及肿瘤的恶性行为仍有待研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36a6/8521387/ce337376cdb9/mco-15-06-02411-g00.jpg

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