Department of Endocrinology and Metabolism, the Affiliated Hospital of Qingdao University, Qingdao, China.
Laboratory for Cellular and Molecular Thyroid Research, Division of Endocrinology, Diabetes & Metabolism, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Clin Endocrinol Metab. 2021 Oct 21;106(11):3228-3238. doi: 10.1210/clinem/dgab286.
How lymph node metastasis (LNM)-associated mortality risk is affected by BRAF V600E in papillary thyroid cancer (PTC) remains undefined.
To study whether BRAF V600E affected LNM-associated mortality in PTC.
DESIGN, SETTING, AND PARTICIPANTS: We retrospectively analyzed the effect of LNM on PTC-specific mortality with respect to BRAF status in 2638 patients (2015 females and 623 males) from 11 centers in 6 countries, with median age of 46 [interquartile range (IQR) 35-58] years and median follow-up time of 58 (IQR 26-107) months.
Overall, LNM showed a modest mortality risk in wild-type BRAF patients but a strong one in BRAF V600E patients. In conventional PTC (CPTC), LNM showed no increased mortality risk in wild-type BRAF patients but a robustly increased one in BRAF V600E patients; mortality rates were 2/659 (0.3%) vs 4/321 (1.2%) in non-LNM vs LNM patients (P = 0.094) with wild-type BRAF, corresponding to a hazard ratio (HR) (95% CI) of 4.37 (0.80-23.89), which remained insignificant at 3.32 (0.52-21.14) after multivariate adjustment. In BRAF V600E CPTC, morality rates were 7/515 (1.4%) vs 28/363 (7.7%) in non-LNM vs LNM patients (P < 0.001), corresponding to an HR of 4.90 (2.12-11.29) or, after multivariate adjustment, 5.76 (2.19-15.11). Adjusted mortality HR of coexisting LNM and BRAF V600E vs absence of both was 27.39 (5.15-145.80), with Kaplan-Meier analyses showing a similar synergism.
LNM-associated mortality risk is sharply differentiated by the BRAF status in PTC; in CPTC, LNM showed no increased mortality risk with wild-type BRAF but a robust one with BRAF mutation. These results have strong clinical relevance.
BRAF V600E 在甲状腺乳头状癌(PTC)中对淋巴结转移(LNM)相关死亡风险的影响仍未明确。
研究 BRAF V600E 是否会影响 PTC 中的 LNM 相关死亡率。
设计、地点和参与者:我们回顾性分析了 11 个中心来自 6 个国家的 2638 例患者(2015 例女性和 623 例男性)的 LNM 对 PTC 特异性死亡率的影响,中位年龄为 46 岁(四分位距 35-58 岁),中位随访时间为 58 个月(四分位距 26-107 个月)。
总体而言,LNM 在野生型 BRAF 患者中显示出适度的死亡率风险,但在 BRAF V600E 患者中显示出强烈的死亡率风险。在经典型甲状腺乳头状癌(CPTC)中,LNM 在野生型 BRAF 患者中未显示出增加的死亡率风险,但在 BRAF V600E 患者中显示出显著增加的死亡率风险;非 LNM 患者的死亡率为 2/659(0.3%),LNM 患者的死亡率为 4/321(1.2%)(P=0.094),野生型 BRAF 患者的风险比(HR)(95%CI)为 4.37(0.80-23.89),经多变量调整后仍无显著性差异(HR 为 3.32(0.52-21.14))。在 BRAF V600E CPTC 中,非 LNM 患者的死亡率为 7/515(1.4%),LNM 患者的死亡率为 28/363(7.7%)(P<0.001),HR 为 4.90(2.12-11.29)或经多变量调整后为 5.76(2.19-15.11)。共存 LNM 和 BRAF V600E 与两者均不存在的调整死亡率 HR 为 27.39(5.15-145.80),Kaplan-Meier 分析显示出类似的协同作用。
LNM 相关死亡风险在 PTC 中因 BRAF 状态而明显分化;在 CPTC 中,野生型 BRAF 时 LNM 不增加死亡率风险,而 BRAF 突变时则显著增加。这些结果具有很强的临床相关性。