Department of Nuclear Medicine, Institut Curie, Saint-Cloud, France.
Department of Pathology, Gustave Roussy and Paris Saclay University, Villejuif, France.
Endocr Relat Cancer. 2022 Sep 30;29(11):625-634. doi: 10.1530/ERC-22-0151. Print 2022 Nov 1.
The prognosis of poorly differentiated thyroid carcinomas (PDTC) defined by the Turin criteria is variable. The aim of this study on 51 PDTC patients was to determine clinical, histological and molecular prognostic factors associated with recurrence in patients with localized disease at initial treatment and with overall survival in patients with distant metastases. Of 40 patients for whom next-generation sequencing (NGS) by ThyroSeq v3 was able to be performed on historical samples, we identified high-risk molecular signature (TERT, TP53 mutations) in 24 (60%) cases, intermediate risk signature in 9 (22.5%) cases and low-risk signature in 7 (17.5%) cases. Potentially actionable mutations were identified in 10% of cases. After a median follow-up of 57.5 months, recurrence occurred in 11 (39%) of the 28 patients with localized disease. The American Thyroid Association (ATA) high risk of relapse, high mitotic count, high molecular risk signature and CD163 expression were associated with recurrence (P = 0.009, 0.01, 0.049, 0.03 respectively). After a median follow-up of 49.5 months, thyroid cancer-related death occurred in 53% of the patients with distant metastases. There was no significant prognostic factor associated with death in univariate analysis. However, none of the patients with intermediate ATA risk of recurrence and none of the patients with low-risk molecular signature died from the disease. In addition, high molecular-risk signature was associated with the presence of synchronous or metachronous distant metastasis (P = 0.007) and with poor overall survival (P = 0.01). In conclusion, ATA risk of relapse and high mitotic count was associated with higher rate of recurrence in localized PDTC. High molecular-risk signature was associated with the presence of distant metastasis and poor overall survival. Further studies are needed to determine if molecular testing adds to ATA risk stratification or response to therapy in predicting outcomes.
根据都灵标准定义的低分化甲状腺癌(PDTC)的预后是可变的。本研究对 51 例 PDTC 患者进行了研究,目的是确定与局部疾病患者的复发和远处转移患者的总体生存率相关的临床、组织学和分子预后因素。在能够对 40 例患者的历史样本进行下一代测序(NGS)的 ThyroSeq v3 中,我们在 24 例(60%)病例中鉴定出高风险分子特征(TERT、TP53 突变),在 9 例(22.5%)病例中鉴定出中风险特征,在 7 例(17.5%)病例中鉴定出低风险特征。在 10%的病例中发现了潜在的可操作突变。在中位随访 57.5 个月后,28 例局部疾病患者中有 11 例(39%)复发。美国甲状腺协会(ATA)的复发高风险、高有丝分裂计数、高分子风险特征和 CD163 表达与复发相关(P = 0.009、0.01、0.049、0.03)。在中位随访 49.5 个月后,远处转移患者中有 53%死于甲状腺癌相关原因。在单因素分析中,没有与死亡相关的显著预后因素。然而,中间 ATA 复发风险和低分子风险特征的患者均未死于疾病。此外,高分子风险特征与同步或异时性远处转移的存在相关(P = 0.007),并且与总体生存不良相关(P = 0.01)。总之,ATA 复发风险和高有丝分裂计数与局部 PDTC 的更高复发率相关。高分子风险特征与远处转移的存在和总体生存不良相关。需要进一步的研究来确定分子检测是否在预测结果方面增加了 ATA 风险分层或对治疗的反应。