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肿瘤大小和分子风险分组与分化型甲状腺癌复发相关。

Tumor size and molecular risk group are associated with differentiated thyroid cancer recurrence.

作者信息

Kurtom Saba, Liu Jason B, Doerfler William R, Calcaterra Michael, McCoy Kelly L, Sada Alaa, Ramonell Kimberly M, Carty Sally E, Nikiforova Marina N, Nikiforov Yuri E, Yip Linwah

机构信息

Division of Endocrine Surgery, Department of Surgery, University of Pittsburgh, PA.

Division of Surgical Oncology, Department of Surgery, Harvard Medical School, Boston, MA.

出版信息

Surgery. 2025 Jan;177:108838. doi: 10.1016/j.surg.2024.06.066. Epub 2024 Oct 9.

Abstract

BACKGROUND

The threshold at which active surveillance can be considered is variable, with some algorithms proposing nonoperative treatment for differentiated thyroid carcinomas ≤2 cm and lobectomy alone for lesions 2.1-4 cm. To inform both decision for and extent of initial surgery, we aim to evaluate whether molecular results can complement tumor size to identify differentiated thyroid carcinomas associated with disease recurrence.

METHODS

Patients from 2007-2013 and 2017-2021 who had initial thyroidectomy (differentiated thyroid carcinoma size 1-4 cm, clinical N0M0) were included. When available, molecular testing results were categorized into 3 previously described molecular risk groups (low, intermediate, and high). Primary outcome was structural recurrence.

RESULTS

Recurrence was diagnosed in 3.8% of 1,739 patients with differentiated thyroid carcinomas. Preoperative variables including size (1-2 cm vs 2.1-4 cm, P = .43), age >55 years (P = .92), and male sex (P = .31) were not associated with recurrence. Molecular testing results were available for 1,020, and after excluding molecular risk group high-risk differentiated thyroid carcinoma, structural recurrences were associated with molecular risk group intermediate risk (7.2% vs molecular risk group low, 0.7%, P < .001), and most likely in differentiated thyroid carcinoma, which were both 2.1-4 cm and molecular risk group intermediate risk (11.3% vs size 1-2 cm 5.8%, P = .04).

CONCLUSION

Overall, structural recurrences for differentiated thyroid carcinomas ≤4 cm were low (<5%) and molecuar testing was the only preoperative variable associated with recurrence. However, when molecular risk group intermediate risk was present, larger tumor size (2.1-4 cm) had a 2-fold greater risk of recurrence compared with tumors 1-2 cm, and size may still be helpful to guide management. When considering de-escalated treatment for the proposed guidelines with a cutoff of 2 cm, initial decision-making may be further optimized with identification of preoperative molecular risk groups.

摘要

背景

可考虑进行主动监测的阈值存在差异,一些算法建议对直径≤2 cm的分化型甲状腺癌采取非手术治疗,对直径2.1 - 4 cm的病灶仅行肺叶切除术。为了为初始手术的决策及其范围提供依据,我们旨在评估分子检测结果是否能补充肿瘤大小,以识别与疾病复发相关的分化型甲状腺癌。

方法

纳入2007 - 2013年以及2017 - 2021年接受初次甲状腺切除术的患者(分化型甲状腺癌大小为1 - 4 cm,临床分期为N0M0)。如有可用的分子检测结果,则将其分为3个先前描述的分子风险组(低、中、高)。主要结局为结构复发。

结果

在1739例分化型甲状腺癌患者中,3.8%被诊断为复发。术前变量包括大小(1 - 2 cm与2.1 - 4 cm,P = 0.43)、年龄>55岁(P = 0.92)和男性(P = 0.31),均与复发无关。1020例患者有分子检测结果,在排除分子风险组高危分化型甲状腺癌后,结构复发与分子风险组中危相关(7.2% vs分子风险组低危,0.7%,P < 0.001),且最可能发生在直径2.1 - 4 cm且分子风险组为中危的分化型甲状腺癌中(11.3% vs大小为1 - 2 cm的5.8%,P = 0.04)。

结论

总体而言,直径≤4 cm的分化型甲状腺癌的结构复发率较低(<5%),分子检测是与复发相关的唯一术前变量。然而,当存在分子风险组中危时,与1 - 2 cm的肿瘤相比,较大肿瘤大小(2.1 - 4 cm)的复发风险高2倍,肿瘤大小可能仍有助于指导治疗。在考虑对拟议的指南采用2 cm的临界值进行降阶梯治疗时,通过识别术前分子风险组,初始决策可能会进一步优化。

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