晚期甲状腺髓样癌患者胆囊收缩素-2/胃泌素受体激动剂刺激后降钙素和降钙素原的测定:来自grant - mtc研究的结果

Małgorzata Trofimiuk-Müldner, Katica Bajuk Studen, Paola Anna Erba, Luka Lezaic, Clemens Decristoforo, Katja Zaletel, Petra Kolenc, Elwira Przybylik-Mazurek, Irene Virgolini, Alide C Fröberg, Anna Skalniak, Renata Mikołajczak, Marion de Jong, Bogdan Solnica, Danuta Fedak, Paulina Gaweda, Christine Rangger, Konrad Skórkiewicz, Alicja Hubalewska-Dydejczyk
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引用次数: 0

摘要

简介:甲状腺髓样癌(MTC)以胆囊收缩素-2/胃泌素受体(CCK2R)过表达为特征。降钙素作为MTC的肿瘤标志物在诊断和预后方面存在局限性。降钙素原正逐渐成为一种补充性的肿瘤标志物。本研究旨在评估MTC患者CCK2R激动剂刺激后降钙素原测量的可行性。材料和方法:该评估是grant -MTC转化研究的一部分,该研究通过一项针对局部晚期和/或弥散性MTC患者的I期多中心临床试验进行。患者静脉给予含有铟-111([¹¹¹In]In-CP04)标记的CCK2R激动剂CP04;前4例患者均为低质量量10 μg,后全组均为高质量量50 μg。在[¹¹¹In]In- cp04给药前和开始后2、5、10和20分钟采集降钙素和降钙素原的血液样本。结果:16例患者纳入研究。注射高质量的[¹¹¹In]In- cp04后,刺激降钙素的中位数最大比值为2.97(四分位间距[IQR] 2.35) pg/mL,降钙素原的中位数最大比值为2.01 (IQR 2.07) pg/mL。低、高质量组最大刺激降钙素/基线比值分别为5.2±4.0和4.1±3.8,低、高质量组最大刺激降钙素/基线比值分别为4.6±5.1和2.9±3.1。各试验时间点降钙素与降钙素原浓度呈显著线性相关(p < 0.001),降钙素原最大值与降钙素最大增量比呈显著线性相关(r = 0.94, p < 0.0001)。1例患者在注射低剂量[¹¹¹in] in - cp04时观察到轻微的、短期的副作用(短暂性心动过速、潮红),2例患者在注射大剂量[¹¹¹in] in - cp04时观察到轻微的、短暂的副作用。副作用与基线降钙素或原降钙素浓度无关。结论:CP04刺激后降钙素原浓度与降钙素浓度高度相关。未标记的CP04,如果可以在市场上买到,可能被认为是MTC患者的一种替代刺激剂,即使是低质量的。需要进一步的研究,包括健康对照,来证明这一概念并计算诊断阈值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calcitonin and procalcitonin measurement after cholecystokinin-2/gastrin receptor agonist stimulation in patients with advanced medullary thyroid cancer: results from the GRAN-T-MTC study.

Introduction: Medullary thyroid cancer (MTC) is characterized by overexpression of cholecystokinin-2/gastrin receptors (CCK2R). There are limitations of calcitonin as a tumor marker in MTC diagnosis and prognosis. Procalcitonin is gaining a role as a complementary tumor marker. This study aimed to assess the feasibility of procalcitonin measurements on top of the calcitonin measurements after CCK2R agonist stimulation in patients with MTC.

Material and methods: The assessment was part of the GRAN-T-MTC translational study conducted through a Phase I multicenter clinical trial in patients with locally advanced and/or disseminated MTC. Patients were administered intravenously the CCK2R agonist CP04 labelled with indium-111 ([¹¹¹In]In-CP04); the first four patients at a lower mass amount of 10 μg, and afterwards the whole group at a higher mass amount of 50 μg. Blood samples for calcitonin and procalcitonin measurements were obtained shortly before and 2, 5, 10, and 20 minutes after start of [¹¹¹In]In-CP04 administration.

Results: Sixteen patients were included in the study. After injection of the higher mass amount of [¹¹¹In]In-CP04, the median maximum ratio for stimulated calcitonin was 2.97 (interquartile range [IQR] 2.35) pg/mL and procalcitonin 2.01 (IQR 2.07) pg/mL. The maximum stimulated/baseline calcitonin ratio was 5.2 ± 4.0 and 4.1 ± 3.8 in the low and high mass amount groups, respectively, and the maximum stimulated/baseline procalcitonin ratio was 4.6 ± 5.1 and 2.9 ± 3.1 in the low and high mass amount groups, respectively. There was a significant linear correlation between calcitonin and procalcitonin concentrations (p < 0.001) at each test time point and between the maximum procalcitonin and maximum calcitonin increment ratio (r = 0.94, p < 0.0001). Mild, short-lasting side effects (transient tachycardia, flushing) were observed in one patient during the injection of low and in two patients during the injection of high mass amount of [¹¹¹In] In-CP04. The side effects were not related to the baseline calcitonin or procalcitonin concentrations.

Conclusion: Procalcitonin concentrations after CP04 stimulation were highly correlated with calcitonin concentrations. Unlabeled CP04, if available commercially, may be considered an alternative stimulating agent in MTC patients, even in lower mass amounts. Further studies, including healthy controls, are required to prove this concept and calculate the diagnostic thresholds.

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