Management and follow-up strategies for patients with head and neck paraganglioma.

IF 5.3 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM European Journal of Endocrinology Pub Date : 2024-09-20 DOI:10.1093/ejendo/lvae113
Susan Richter, Karel Pacak, Henricus Kunst, Andrzej Januszewicz, Svenja Nölting, Hanna Remde, Mercedes Robledo, Graeme Eisenhofer, Henri J Timmers, Christina Pamporaki
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Abstract

Objective: Head-neck paragangliomas (HNPGLs) are rare tumors with approximately half arising due to germline pathogenic variants (PVs) in succinate dehydrogenase genes (SDHx). Patients with HNPGL have heterogenous propensity to recur and metastasize. Thus, we aim to assess prevalence and predictors of recurrent (RD) and/or metastatic disease in patients with and without SDHx-related HNPGLs.

Design and methods: This cross-sectional study used retrospective data of 214 patients enrolled in six referral centers. Data included sex, age, primary tumor treatment, location, and size, biochemical phenotype, germline PVs, presence of RD (locoregional or new tumor), and/or metastasis.

Results: Patients with and without SDHx-related HNPGLs showed 74% and 40% prevalence of RD, respectively. Patients without SDHx-related HNPGLs presented with recurrent tumors only in head-neck regions. The only independent predictor for RD in the entire cohort was presence of SDHx PVs. Metastatic prevalence reached 9-13%. For patients with SDHx-related HNPGLs, large tumor size (>2.3cm, OR:50.0, CI:2.6-977.6), young age at initial diagnosis (<42years, OR:27.3, CI:1.8-407.2), and presence of SDHB PV (OR:15.6; CI:1.5-164.8) were independent predictors of metastasis. For patients without SDHx-related HNPGLs, only carotid-body location was an independent predictor of metastasis (OR:18.9, CI:2.0-182.5).

Conclusions: Patients without SDHx-related HNPGLs require long-term follow-up due to high prevalence of RD with imaging largely restricted to head-neck regions. As carotid-body HNPGLs have the highest metastatic risk among sporadic tumors, radical treatment with frequent follow-up is suggested until population-based data are available. Importantly, patients with SDHx-related HNPGLs might benefit from early radical treatment when tumors are still small to reduce metastatic risk.

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头颈部副神经节瘤患者的管理和随访策略。
目的:头颈部副神经节瘤(HNPGL)是一种罕见肿瘤,约有一半是由于琥珀酸脱氢酶基因(SDHx)的种系致病变体(PVs)引起的。HNPGL 患者具有不同的复发和转移倾向。因此,我们旨在评估与SDHx相关和不相关的HNPGL患者中复发(RD)和/或转移性疾病的患病率和预测因素:这项横断面研究使用了六个转诊中心登记的 214 例患者的回顾性数据。数据包括性别、年龄、原发肿瘤的治疗、位置和大小、生化表型、种系PV、是否存在RD(局部或新发肿瘤)和/或转移:结果:有SDHx相关HNPGLs和无SDHx相关HNPGLs患者的RD发生率分别为74%和40%。无SDHx相关HNPGLs的患者仅在头颈部出现复发性肿瘤。在整个队列中,存在SDHx PV是RD的唯一独立预测因素。转移率达到 9-13%。无SDHx相关HNPGLs的患者需要长期随访,因为RD的发病率很高,且成像主要局限于头颈部。由于颈动脉体部 HNPGL 在散发性肿瘤中具有最高的转移风险,因此在获得基于人群的数据之前,建议进行根治性治疗并经常随访。重要的是,与SDHx相关的HNPGL患者可在肿瘤尚小时接受早期根治性治疗,以降低转移风险。
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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来源期刊
European Journal of Endocrinology
European Journal of Endocrinology 医学-内分泌学与代谢
CiteScore
9.80
自引率
3.40%
发文量
354
审稿时长
1 months
期刊介绍: European Journal of Endocrinology is the official journal of the European Society of Endocrinology. Its predecessor journal is Acta Endocrinologica. The journal publishes high-quality original clinical and translational research papers and reviews in paediatric and adult endocrinology, as well as clinical practice guidelines, position statements and debates. Case reports will only be considered if they represent exceptional insights or advances in clinical endocrinology. Topics covered include, but are not limited to, Adrenal and Steroid, Bone and Mineral Metabolism, Hormones and Cancer, Pituitary and Hypothalamus, Thyroid and Reproduction. In the field of Diabetes, Obesity and Metabolism we welcome manuscripts addressing endocrine mechanisms of disease and its complications, management of obesity/diabetes in the context of other endocrine conditions, or aspects of complex disease management. Reports may encompass natural history studies, mechanistic studies, or clinical trials. Equal consideration is given to all manuscripts in English from any country.
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