Progastrin-Releasing Peptide and Procalcitonin as Additional Markers in the Diagnostic Workup for Medullary Thyroid Carcinoma.

IF 6.7 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Thyroid Pub Date : 2025-06-27 DOI:10.1089/thy.2024.0293
Leonoor E Schonebaum, Sjoerd A A van den Berg, Mathé van Balkum, W Edward Visser, Luca Giovanella, Robin P Peeters
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引用次数: 0

Abstract

Background: Calcitonin (CT), a well-established tumor marker for medullary thyroid carcinoma (MTC), is limited by a high rate of false positives in the diagnostic phase. Potential new markers for MTC are procalcitonin (PCT) and progastrin-releasing peptide (proGRP). Where literature has proven noninferiority for PCT, evidence is lacking for proGRP. Therefore, the present study prospectively evaluated the clinical performance of proGRP and PCT in a multicohort study of patients with MTC compared with other thyroid diseases. Methods: Adult patients undergoing thyroid surgery for thyroid nodular disease diagnosed in a tertiary center from the Netherlands (discovery cohort) between 2013 and 2025 were prospectively included. Serum samples were collected preoperatively. Diagnostic performance of CT, PCT, proGRP, and carcinoembryonic antigen was calculated separately. A two-step approach, combining different markers, was investigated. Analyses were repeated in a validation cohort from Switzerland. Results: The discovery and validation cohorts consisted of 335 and 61 patients, respectively. Patients had benign disease (n = 166), other thyroid carcinomas (non-MTC, n = 186), or MTC (n = 44). Median proGRP and PCT levels were significantly higher in MTC compared with benign disease and non-MTC. ProGRP had a low sensitivity (69.2% [CI 48.2-85.7]), while PCT performed similarly to CT (100.0% [CI 89.1-100.0] and 100.0% [CI 88.8-100.0], respectively). The combination of CT and PCT, both in the individual cohorts and when combining the two cohorts, showed the best diagnostic performance with a sensitivity of 100% [CI 91.8-100.0] and negative predictive value of 100% [CI 98.9-100.0] and specificity and positive predictive value of 99.7% [CI 98.4-100.0] and 97.7% [CI 88.0-99.9], respectively. Conclusions: ProGRP alone or with CT does not have additional value as a diagnostic marker for MTC. A two-step approach combining the use of CT and PCT measurement, in the CT concentration range between 10 and 100 pg/mL, is a promising method to diagnose MTC in patients with thyroid nodules with high diagnostic accuracy.

原胃泌素释放肽和降钙素原作为甲状腺髓样癌诊断检查的附加标志物。
背景:降钙素(CT)是一种公认的甲状腺髓样癌(MTC)的肿瘤标志物,但在诊断阶段被高假阳性率所限制。潜在的MTC新标志物是降钙素原(PCT)和原胃泌素释放肽(proGRP)。文献已证明PCT无劣效性,但缺乏关于proGRP的证据。因此,本研究前瞻性地评价了proGRP和PCT在MTC患者与其他甲状腺疾病患者的多队列研究中的临床表现。方法:前瞻性纳入2013年至2025年间在荷兰三级中心诊断的甲状腺结节性疾病接受甲状腺手术的成年患者(发现队列)。术前采集血清样本。分别计算CT、PCT、proGRP、癌胚抗原的诊断效能。研究了一种两步法,结合不同的标记物。在瑞士的验证队列中重复分析。结果:发现组和验证组分别包括335例和61例患者。患者有良性疾病(n = 166)、其他甲状腺癌(n = 186)或甲状腺癌(n = 44)。与良性疾病和非MTC相比,MTC的中位proGRP和PCT水平显著升高。ProGRP的敏感性较低(69.2% [CI 48.2-85.7]),而PCT的敏感性与CT相似(分别为100.0% [CI 89.1-100.0]和100.0% [CI 88.8-100.0])。CT与PCT联合使用,无论是在个体队列中还是在两组联合使用时,均表现出最佳的诊断效果,其敏感性为100% [CI 91.8-100.0],阴性预测值为100% [CI 98.9-100.0],特异性和阳性预测值分别为99.7% [CI 98.4-100.0]和97.7% [CI 88.0-99.9]。结论:ProGRP单独或与CT联合作为MTC的诊断指标没有额外的价值。两步法结合CT和PCT测量,在CT浓度范围在10 ~ 100 pg/mL之间,是诊断甲状腺结节患者MTC的一种有前景的方法,诊断准确率高。
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来源期刊
Thyroid
Thyroid 医学-内分泌学与代谢
CiteScore
12.30
自引率
6.10%
发文量
195
审稿时长
6 months
期刊介绍: This authoritative journal program, including the monthly flagship journal Thyroid, Clinical Thyroidology® (monthly), and VideoEndocrinology™ (quarterly), delivers in-depth coverage on topics from clinical application and primary care, to the latest advances in diagnostic imaging and surgical techniques and technologies, designed to optimize patient care and outcomes. Thyroid is the leading, peer-reviewed resource for original articles, patient-focused reports, and translational research on thyroid cancer and all thyroid related diseases. The Journal delivers the latest findings on topics from primary care to clinical application, and is the exclusive source for the authoritative and updated American Thyroid Association (ATA) Guidelines for Managing Thyroid Disease.
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