Pediatric Papillary Thyroid Carcinoma: Outcomes After Surgery Without Adjuvant Radioactive Iodine.

IF 5 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Clinical Endocrinology & Metabolism Pub Date : 2025-01-21 DOI:10.1210/clinem/dgae576
Luz E Castellanos, Mark E Zafereo, Erich M Sturgis, Jennifer R Wang, Anita K Ying, Steven G Waguespack
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Abstract

Context: Pediatric papillary thyroid carcinoma (PTC) is usually treated with total thyroidectomy followed by radioactive iodine (RAI). Recently, RAI has been used more selectively based on surgical pathology and postoperative dynamic risk stratification (DRS).

Objective: To describe patients with pediatric PTC not initially treated with RAI and their disease outcomes.

Methods: This was an ambispective study at a tertiary cancer center of patients < 19 years diagnosed from January 1, 1990, to December 31, 2021, with stage 1 PTC who intentionally were not treated with RAI within a year of diagnosis. We assessed clinical characteristics, management, and disease outcomes using DRS.

Results: Of 490 PTC patients, we identified 93 eligible patients (median age at diagnosis 16 years; 87% female), including 46 (49%) with cervical lymph node metastases. Initial management included total thyroidectomy ± neck dissection (n = 69, 75%), lobectomy ± neck dissection (n = 20, 21%), or a Sistrunk procedure for ectopic PTC (n = 4, 4%). After a median follow-up of 5.5 years (range 1-26), most patients (85/93; 91%) remained disease-free with no further therapy. Persistent (n = 5) or recurrent (n = 3) disease was found in 9% of the entire cohort. Four patients ultimately received RAI, of which only 1 clearly benefitted, and additional surgery was performed or planned in 4 patients, 2 of whom had an excellent response at last follow-up.

Conclusion: Selected pediatric PTC patients, even those with lymph node metastases, may not require therapeutic 131I and can avoid the unnecessary risks of RAI while still benefitting from the excellent long-term outcomes that are well described for this disease.

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小儿甲状腺乳头状癌:无辅助放射性碘手术后的疗效
背景:小儿甲状腺乳头状癌(PTC)通常采用甲状腺全切除术,然后使用放射性碘(RAI)治疗。最近,根据手术病理和术后动态风险分层(DRS),RAI的使用更具选择性:描述最初未接受 RAI 治疗的儿科 PTC 患者及其疾病预后:这是在一家三级癌症中心进行的一项前瞻性研究,研究对象是1990年1月1日至2021年12月31日期间确诊的小于19岁的I期PTC患者,这些患者在确诊后一年内故意未接受RAI治疗。我们使用 DRS 评估了这些患者的临床特征、管理和疾病预后:在 490 例 PTC 患者中,我们确定了 93 例符合条件的患者(诊断时的中位年龄为 16 岁;87% 为女性),其中 46 例(49%)有颈淋巴结转移。初始治疗包括:甲状腺全切除术±颈部清扫术(69例,75%)、甲状腺叶切除术±颈部清扫术(20例,21%)或针对异位PTC的Sistrunk手术(4例,4%)。中位随访 5.5 年(1-26 年不等)后,大多数患者(85/93;91%)仍未发病,且未接受进一步治疗。整个组群中有 9% 的患者病情持续(5 人)或复发(3 人)。四名患者最终接受了 RAI 治疗,其中只有一人明显获益,另有四名患者接受或计划接受手术治疗,其中两人在最后一次随访时反应极佳:结论:经过选择的儿科 PTC 患者,即使是有淋巴结转移的患者,也可能不需要 131I 治疗,并且可以避免 RAI 带来的不必要风险,同时还能从该疾病的良好长期疗效中获益。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
期刊最新文献
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