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伴有可触及侧颈部淋巴结转移的甲状腺微小乳头状癌的结局。

Outcomes of Papillary Thyroid Microcarcinoma Presenting with Palpable Lateral Lymphadenopathy.

机构信息

Endocrine Surgical Unit, Royal North Shore Hospital, St Leonards, New South Wales, Australia.

Northern Clinical School, Sydney Medical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Thyroid. 2022 Sep;32(9):1086-1093. doi: 10.1089/thy.2022.0109. Epub 2022 Jul 21.

Abstract

Papillary thyroid microcarcinoma (PTMC) is typically indolent in nature, allowing management with active surveillance protocols. Occasionally, a more aggressive phenotype can present and may lead to poor outcomes such as patients presenting with clinically significant lateral lymphadenopathy (cN1b). Prior analysis of the outcomes of this cohort is largely from papillary thyroid cancer (PTC) (>1 cm) or from institutions where use of radioactive iodine (RAI) is limited. Hence, we aim to describe the outcomes of patients with PTMC who presented with palpable cN1b disease, treated with total thyroidectomy and RAI. We performed a retrospective cohort study. Outcomes of patients with PTMC who presented with palpable lateral lymph node (LN) metastases (microPTC cN1b) treated between 1997 and 2020 at Royal North Shore Hospital were compared with two control groups' outcomes: patients with clinically detected PTMC without evidence of involved LNs (microPTC cN0) and with larger PTC (>10 mm) who presented with palpable lateral lymphadenopathy (larger PTC cN1b). We assessed clinicopathological variables, postoperative risk stratification, rates of disease recurrence, reoperative surgery, and structural disease-free survival (DFS). In total, 1534 PTMCs were diagnosed following thyroid surgery in the study period; of these, 157 (10%) were clinically detected microPTC cN0 and 26 microPTC cN1b (1.7%). There were 138 patients in the larger PTC cN1b control group. All cN1b patients were treated with total thyroidectomy and adjuvant RAI. Mean size of the largest LN deposit was similar between the microPTC cN1b and larger PTC cN1b groups (23 vs. 27 mm,  = 0.11). Patients with microPTC cN1b were more likely to have biochemical or structural persistence or recurrence compared with microPTC cN0 (19%, 5/26 vs. 3.8%, 6/157,  = 0.002) but less likely than larger PTC cN1b patients (19%, 5/26 vs. 42%, 58/138,  = 0.04). All patients in the microPTC cN1b group who had an excellent response to initial therapy (85%, 22/26) were disease free at last follow-up. The rate of reoperation was similar for the microPTC cN1b and microPTC cN0 groups (4%, 1/26 vs. 2%, 3/157,  = 0.461) and significantly lower than the larger PTC cN1b group (4%, 1/26 vs. 26%, 36/138,  = 0.002). Five-year DFS estimates were significantly better for microPTC cN1b patients than for larger PTC cN1b patients (94% vs. 59%,  = 0.001). MicroPTC cN1b patients treated with thyroidectomy and adjuvant RAI have inferior clinical outcomes compared with microPTC cN0 patients but have better outcomes than their larger PTC cN1b counterparts with respect to disease persistence and recurrence. Response to initial therapy provides valuable prognostication in microPTC cN1b patients: if these patients had an excellent response to initial treatment, they achieved long-term DFS in this series.

摘要

甲状腺微小乳头状癌(PTMC)通常为惰性,可通过主动监测方案进行管理。偶尔,更具侵袭性的表型可能会出现,并可能导致不良结局,例如患者出现临床显著的侧方淋巴结转移(cN1b)。先前对该队列的结局分析主要来自甲状腺乳头状癌(PTC)(>1cm)或放射性碘(RAI)使用受限的机构。因此,我们旨在描述经总甲状腺切除术和 RAI 治疗的出现可触及 cN1b 疾病的 PTMC 患者的结局。我们进行了一项回顾性队列研究。比较了 1997 年至 2020 年期间在皇家北岸医院接受治疗的出现可触及侧方淋巴结(LN)转移(微 PTMC cN1b)的 PTMC 患者与两个对照组的结局:临床发现的无受累 LNs 的微 PTMC cN0 患者(微 PTMC cN0)和出现可触及侧方淋巴结病的较大 PTC(>10mm)患者(较大 PTC cN1b)。我们评估了临床病理变量、术后风险分层、疾病复发率、再次手术和结构无病生存率(DFS)。研究期间,在甲状腺手术后共诊断出 1534 例 PTMC;其中,157 例(10%)为临床发现的微 PTMC cN0,26 例为微 PTMC cN1b(1.7%)。较大 PTC cN1b 对照组有 138 例患者。所有 cN1b 患者均接受了全甲状腺切除术和辅助 RAI。微 PTMC cN1b 和较大 PTC cN1b 组最大 LN 沉积的平均大小相似(23 与 27mm,=0.11)。与微 PTMC cN0 相比,微 PTMC cN1b 患者更有可能出现生化或结构持续存在或复发(19%,5/26 与 3.8%,6/157,=0.002),但低于较大 PTC cN1b 患者(19%,5/26 与 42%,58/138,=0.04)。初始治疗有良好反应的微 PTMC cN1b 组所有患者(85%,22/26)在最后一次随访时均无疾病。微 PTMC cN1b 组和微 PTMC cN0 组的再次手术率相似(4%,1/26 与 2%,3/157,=0.461),明显低于较大 PTC cN1b 组(4%,1/26 与 26%,36/138,=0.002)。微 PTMC cN1b 患者的 5 年 DFS 估计明显优于较大 PTC cN1b 患者(94%与 59%,=0.001)。经甲状腺切除术和辅助 RAI 治疗的微 PTMC cN1b 患者与微 PTMC cN0 患者相比临床结局较差,但与较大 PTC cN1b 患者相比,其疾病持续存在和复发的结局较好。初始治疗的反应为微 PTMC cN1b 患者提供了有价值的预后:如果这些患者对初始治疗有良好的反应,他们在本系列中实现了长期 DFS。

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