Clinical characteristics and prognosis of histological subtypes of papillary thyroid carcinoma in pediatric patients.

Endocrine oncology (Bristol, England) Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.1530/EO-24-0078
Junko Akaishi, Kiminori Sugino, Tetsuo Kondo, Wataru Kitagawa, Kenichi Matsuzu, Akifumi Suzuki, Chisato Tomoda, Ritsuko Okamura, Kiyomi Y Hames, Chie Masaki, Yoshiyuki Saito, Kana Yoshioka, Kosuke Inoue, Ryohei Katoh, Koichi Ito
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Abstract

The purpose of this study was to clarify the clinicopathological features and prognosis of histological subtypes of papillary thyroid carcinoma (PTC) in the pediatric population treated at a single institution. A total of 153 PTC patients ≤18 years of age who underwent initial surgery between 1979 and 2019 were investigated. There were 135 female and 18 male patients, with a mean age at the time of surgery of 16 (range, 8-18) years. The most common subtypes included classic PTC in 124 (81%), solid variant in 16 (10%), diffuse sclerosing variant in 7 (5%) and follicular variant in six (4%) according to the 5th edition of the WHO classification. At initial surgery, 49 patients (32%) had clinical lymph node metastases (cN1), 137 patients (90%) had pathological lymph node metastases (pN1), 73 patients (48%) had number of lymph node metastases (NLNMs) ≥10, 16 (10%) had gross extrathyroidal extension (ETE) and 18 (12%) had lung metastases. During a mean follow-up of 16 years, three (2%) patients died of their disease and 34 (25%) patients had recurrent disease. The 30-year cause-specific survival rate was 97.2%, and the 30-year disease-free survival (DFS) rate was 65.0%. On multivariate analysis, gross ETE, cN1 and NLNMs ≥10 identified as significant factors related to DFS (hazard ratio (HR) 4.13, confidence interval (CI) 1.48-9.96, P = 0.009; HR 2.34, CI 1.09-4.95, P = 0.0293; HR 2.81, CI 1.30-6.59, P = 0.008), but not histological subtype, were associated with disease recurrence. Histological subtypes were not associated with disease recurrence, but long-term follow-up of pediatric patients is necessary to investigate the biological characteristics.

Synopsis: This retrospective study investigated the clinicopathological features and clinical outcomes of histological subtypes of PTC in a large series of pediatric patients treated at a single institution. It found that the prognosis of pediatric patients with PTC was excellent, but recurrence was common. In pediatric PTC, histological subtype did not affect survival and recurrence.

小儿甲状腺乳头状癌组织学亚型的临床特点及预后。
本研究的目的是阐明在单一机构治疗的儿科人群中甲状腺乳头状癌(PTC)的组织学亚型的临床病理特征和预后。本研究共调查了1979年至2019年间接受首次手术的153例≤18岁的PTC患者。女性135例,男性18例,手术时平均年龄16岁(范围8-18岁)。根据世卫组织第五版分类,最常见的亚型包括124例(81%)的经典PTC, 16例(10%)的实型变异,7例(5%)的弥漫性硬化型和6例(4%)的滤泡型变异。手术初期,49例(32%)患者有临床淋巴结转移(cN1), 137例(90%)患者有病理性淋巴结转移(pN1), 73例(48%)患者淋巴结转移数(NLNMs)≥10个,16例(10%)患者有甲状腺外展(ETE), 18例(12%)患者有肺转移。在平均16年的随访期间,3例(2%)患者死于疾病,34例(25%)患者复发。30年病因特异性生存率为97.2%,30年无病生存率(DFS)为65.0%。在多因素分析中,gross ETE、cN1和NLNMs≥10被确定为与DFS相关的显著因素(风险比(HR) 4.13,置信区间(CI) 1.48 ~ 9.96, P = 0.009;Hr 2.34, ci 1.09-4.95, p = 0.0293;HR 2.81, CI 1.30-6.59, P = 0.008),但组织学亚型与疾病复发无关。组织学亚型与疾病复发无相关性,但对患儿的生物学特征进行长期随访是必要的。摘要:本回顾性研究调查了在同一医院接受治疗的大量儿科患者的PTC组织学亚型的临床病理特征和临床结果。发现小儿PTC患者预后良好,但复发率较高。在儿童PTC中,组织学亚型不影响生存和复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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