Germline genetic variants in pheochromocytoma/paraganglioma: single-center experience.

José V Lima, Nilza M Scalissi, Kelly C de Oliveira, Susan C Lindsey, Caroline Olivati, Elisa Napolitano Ferreira, Claudio E Kater
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Abstract

Pheochromocytoma and paragangliomas (PPGLs) are rare neuroendocrine tumors carrying 25-40% pathogenic germline gene variants (PGVs). We evaluated clinical, laboratory, and germline molecular profile of 115 patients with pathologic (14 patients were relatives from 8 different families recruited for genetic survey) confirmed PPGL followed in our institution. Patients with classic MEN2A/MEN2B phenotypes and at-risk relatives underwent direct analysis of RET proto-oncogene, and the remaining had samples submitted to complete next-generation sequencing aiming 23 PPGL-related genes: ATM, ATR, CDKN2A, EGLN1, FH, HRAS, KIF1B, KMT2D, MAX, MDH2, MERTK, MET, NF1, PIK3CA, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127, TP53, and VHL. We also developed a clinical judgment score (CJS) to determine the probability of patients having a potentially hereditary disease. The resulting genetic landscape showed that 67 patients (58.3%) had variants in at least one gene: 34 (50.7%) had exclusively pathogenic or likely pathogenic variants, 13 (19.4%) had pathogenic or likely pathogenic variants and variant of undetermined significance (VUS), and 20 (29.8%) carried only VUS. PGVs were found in RET (n = 18; 38.3%), VHL (n = 10; 21.3%), SDHB and NF1 (n = 8; 17% each), and MAX, SDHD, TMEM127, and TP53 (n = 1; 2.1% each). Direct genetic testing disclosed 91.3% sensitivity, 81.2% specificity, and 76.4% and 93.3% positive predictive value (PPV) and negative predictive values (NPV), respectively. The CJS to identify patients who would not benefit from genetic testing had 75% sensitivity, 96.4% specificity, and 60% and 98.2% PPV and NPV, respectively. In summary, the landscape of PPGL germline gene variants from 115 Brazilian patients resulted in slightly higher prevalent pathogenic and likely pathogenic variants, especially in the RET gene. We suggest a CJS to identify PPGL patients who would not require initial genetic evaluation, improving test specificity and reducing costs.

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嗜铬细胞瘤/副神经节瘤的生殖系遗传变异:单中心经验。
嗜铬细胞瘤和副神经节瘤(PPGLs)是一种罕见的神经内分泌肿瘤,携带25-40%致病性种系基因变异(PGVs)。我们评估了我院115例病理确诊PPGL患者的临床、实验室和种系分子谱(其中14例患者来自8个不同家庭的亲属进行遗传调查)。典型MEN2A/MEN2B表型和高危亲属的患者直接分析RET原癌基因,其余患者将样品提交完成针对23个ppgl相关基因的下一代测序:ATM, ATR, CDKN2A, EGLN1, FH, HRAS, KIF1B, KMT2D, MAX, MDH2, MERTK, MET, NF1, PIK3CA, RET, SDHA, shaf2, SDHB, SDHC, SDHD, TMEM127, TP53和VHL。我们还开发了临床判断评分(CJS)来确定患者患有潜在遗传性疾病的可能性。结果显示,67例(58.3%)患者至少有一个基因变异,34例(50.7%)患者有完全致病或可能致病的变异,13例(19.4%)患者有致病或可能致病的变异和不确定意义的变异(VUS), 20例(29.8%)患者仅携带VUS。在RET中发现了PGVs (n = 18;38.3%), VHL (n = 10;21.3%)、SDHB和NF1 (n = 8;MAX、sddd、TMEM127和TP53 (n = 1;2.1%)。直接基因检测敏感性为91.3%,特异性为81.2%,阳性预测值(PPV)和阴性预测值(NPV)分别为76.4%和93.3%。CJS识别不能从基因检测中获益的患者的敏感性为75%,特异性为96.4%,PPV和NPV分别为60%和98.2%。综上所述,来自115名巴西患者的PPGL种系基因变异导致流行致病性和可能致病性变异略高,尤其是RET基因。我们建议使用CJS来识别不需要初始遗传评估的PPGL患者,从而提高检测特异性并降低成本。
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