Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Division of Endocrinology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Histopathology. 2021 Sep;79(3):427-436. doi: 10.1111/his.14370. Epub 2021 Jun 15.
Tumour grade and RET mutation status, especially the presence of high-risk exon 15 and 16 RET mutations, have been reported to be prognostic in patients with sporadic medullary thyroid carcinoma (MTC). The aims of our study were to evaluate the performance of two recently proposed grading systems and to assess the association between grade and genotype in a cohort of sporadic MTCs.
We identified 44 sporadic MTCs. All available tumour slides were examined, and cases were assigned a grade on the basis of either mitotic count and tumour necrosis, or mitotic count, tumour necrosis, and Ki-67 proliferative index, as described in two recent studies. Additional clinicopathological features and outcome information were obtained from the pathology reports and electronic medical records. The presence of RET and RAS mutations was determined either with direct sequencing or with massively parallel sequencing. Both grading systems were prognostic for progression-free survival and disease-specific survival on univariate analysis. There was no correlation between grade and mutation status. Specifically, neither RET nor high-risk RET mutations were enriched in high-grade tumours, as assessed by either grading scheme.
Our findings suggest that grade is not correlated with RET/RAS mutation status, indicating that grade and genotype may give independent prognostic information.
肿瘤分级和 RET 突变状态,特别是存在高风险的外显子 15 和 16 RET 突变,已被报道在散发性甲状腺髓样癌(MTC)患者中具有预后意义。我们的研究目的是评估两种最近提出的分级系统的性能,并在散发性 MTC 队列中评估分级与基因型之间的关联。
我们确定了 44 例散发性 MTC。根据最近两项研究中描述的有丝分裂计数和肿瘤坏死或有丝分裂计数、肿瘤坏死和 Ki-67 增殖指数,对所有可用的肿瘤切片进行了检查,并对病例进行了分级。从病理报告和电子病历中获得了其他临床病理特征和结局信息。通过直接测序或大规模平行测序确定了 RET 和 RAS 突变的存在。两种分级系统在单因素分析中均对无进展生存期和疾病特异性生存期具有预后意义。分级与突变状态之间没有相关性。具体来说,两种分级方案均未显示高分级肿瘤中富集 RET 或高风险 RET 突变。
我们的发现表明,分级与 RET/RAS 突变状态无关,表明分级和基因型可能提供独立的预后信息。