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启动子突变与第八版TNM分类在预测甲状腺癌患者生存中的作用

Promoter Mutations and the 8th Edition TNM Classification in Predicting the Survival of Thyroid Cancer Patients.

作者信息

Park Jun, Lee Sungjoo, Kim Kyunga, Park Hyunju, Ki Chang-Seok, Oh Young Lyun, Shin Jung Hee, Kim Jee Soo, Kim Sun Wook, Chung Jae Hoon, Kim Tae Hyuk

机构信息

Division of Endocrinology & Metabolism, Department of Medicine, Thyroid Center, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul 06351, Korea.

Department of Digital Health, Samsung Advanced Institute for Health Sciences & Technology, School of Medicine, Sungkyunkwan University, Seoul 06351, Korea.

出版信息

Cancers (Basel). 2021 Feb 5;13(4):648. doi: 10.3390/cancers13040648.

Abstract

Our research group has previously shown that the presence of promoter mutations is an independent prognostic factor, by applying the mutation status to the variables of the AJCC 7th edition. This study aimed to determine if mutations could be independent predictors of thyroid cancer-specific mortality based on the AJCC TNM 8th edition, with long-term follow-up. This was a retrospective study of 393 patients with pathologically confirmed differentiated thyroid carcinoma (DTC) after thyroidectomy at a tertiary Korean hospital from 1994 to 2004. The thyroid cancer-specific mortality rate was 6.9% (5.2% for papillary and 15.2% for follicular cancers). promoter mutations were identified in 10.9% (43/393) of DTC cases (9.8% of papillary and 16.7% of follicular cancer) and were associated with older age ( < 0.001), the presence of extrathyroidal invasion ( < 0.001), distant metastasis ( = 0.001), and advanced stage at diagnosis ( < 0.001). The 10-year survival rate in mutant was 67.4% for DTC patients (vs. 98% for wild-type; adjusted hazard ratio (HR) of 9.93, (95% CI: 3.67-26.90)) and 75% for patients with papillary cancer (vs. 99%; 18.55 (4.83-71.18)). In addition, promoter mutations were related to poor prognosis regardless of histologic type ( < 0.001 for both papillary and follicular cancer) or initial stage ( < 0.001, = 0.004, and = 0.086 for stages I, II, and III and IV, respectively). promoter mutations comprise an independent poor prognostic factor after adjusting for the clinicopathological risk factors of the AJCC TNM 8th edition, histologic type, and each stage at diagnosis, which could increase prognostic predictability for patients with DTC.

摘要

我们的研究小组先前通过将启动子突变状态应用于美国癌症联合委员会(AJCC)第7版的变量,表明启动子突变的存在是一个独立的预后因素。本研究旨在基于AJCC TNM第8版并进行长期随访,确定启动子突变是否可能是甲状腺癌特异性死亡的独立预测因素。这是一项对1994年至2004年在韩国一家三级医院接受甲状腺切除术后病理确诊为分化型甲状腺癌(DTC)的393例患者的回顾性研究。甲状腺癌特异性死亡率为6.9%(乳头状癌为5.2%,滤泡状癌为15.2%)。在10.9%(43/393)的DTC病例中发现了启动子突变(乳头状癌为9.8%,滤泡状癌为16.7%),且与年龄较大(<0.001)、甲状腺外侵犯的存在(<0.001)、远处转移(=0.001)以及诊断时的晚期阶段(<0.001)相关。对于DTC患者,启动子突变型的10年生存率为67.4%(野生型为98%;调整后的风险比(HR)为9.93,(95%可信区间:3.67 - 26.90)),对于乳头状癌患者为75%(野生型为99%;18.55(4.83 - 71.18))。此外,无论组织学类型(乳头状癌和滤泡状癌均<0.001)或初始阶段(I、II、III和IV期分别为<0.001、=0.004和=0.086)如何,启动子突变均与预后不良相关。在调整了AJCC TNM第8版的临床病理危险因素、组织学类型以及诊断时的各个阶段后,启动子突变构成了一个独立的不良预后因素,这可以提高DTC患者的预后预测能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abb7/7915040/150ad6d385e4/cancers-13-00648-g001.jpg

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