Université de Paris, Department of Gastroenterology-Pancreatology, ENETS Centre of Excellence, Hôpital Beaujon (APHP), Clichy, France.
Biochemistry and Genetic Laboratory, Federative Institute of Biology, Hôpital Purpan and Université Toulouse III Paul Sabatier, Inserm, Toulouse, France.
J Clin Endocrinol Metab. 2021 Mar 25;106(4):e1673-e1682. doi: 10.1210/clinem/dgaa924.
Although 24-hour urinary 5-hydroxyindolacetic acid (24u5HIAA) is a key biomarker in midgut neuroendocrine tumors (NETs), it may be inaccurate and inconvenient.
We compared the diagnostic performances of 24u5HIAA, overnight urinary 5HIAA (Ou5HIAA), and plasmatic 5HIAA (p5HIAA) in midgut NETs.
This prospective, multicenter study included 80 patients with metastatic midgut NETs and 17 control patients with irritable bowel syndrome. 24u5HIAA, Ou5HIAA, and p5HIAA were measured in urine and plasma collected on 2 consecutive days following a specific recommended diet. Reproducibility of the biomarkers was evaluated by the Spearman test. Diagnostic performance was assessed by the area under the receiver operating characteristic curve (AUROC). Correlations with the main clinical features and declared observance to the specific diet were assessed using AUROC and logistic regression models.
The reproducibility of 24u5HIAA, Ou5HIAA, and p5HIAA were excellent (ρ = 0.916; 0.897; 0.978, respectively, P < .001) with significant discrimination between patients and controls (AUROC = 0.795, P < .001; 0.757, P = .001; 0.717, P = .005, respectively). All 3 markers were correlated with the presence of carcinoid syndrome (AUROC = 0.702, P = .006; 0.701, P = .006; 0.697, P = .007, respectively), carcinoid heart disease (AUROC = 0.896; 0.887; 0.923, P < .001, respectively, P < .001), and liver metastatic involvement greater than 30% (AUROC = 0.827; 0.807; 0.849, P < .001, respectively, P < .001), independent from other traditional prognostic factors. Biomarker levels were similar between patients with optimal or suboptimal diet observance.
Ou5HIAA and p5HIAA could be used as more convenient alternatives to 24u5HIAA in patients with metastatic midgut NETs. Prospective long-term studies with repeated dosages are needed.
24 小时尿 5-羟吲哚乙酸(24u5HIAA)是一种用于诊断类癌的关键生物标志物,但其可能存在不准确性和不便利性。
我们比较了 24u5HIAA、夜间尿 5HIAA(Ou5HIAA)和血浆 5HIAA(p5HIAA)在诊断类癌中的性能。
这是一项前瞻性、多中心研究,共纳入 80 例转移性中肠类癌患者和 17 例对照的肠易激综合征患者。在连续两天遵循特定的推荐饮食后,收集尿液和血浆,以测量 24u5HIAA、Ou5HIAA 和 p5HIAA。通过 Spearman 检验评估生物标志物的可重复性。通过接收者操作特征曲线下的面积(AUROC)评估诊断性能。使用 AUROC 和逻辑回归模型评估与主要临床特征的相关性以及对特定饮食的遵守情况。
24u5HIAA、Ou5HIAA 和 p5HIAA 的可重复性极好(ρ=0.916;0.897;0.978,P<0.001),患者与对照组之间存在显著差异(AUROC=0.795,P<0.001;0.757,P=0.001;0.717,P=0.005)。所有 3 种标志物均与类癌综合征(AUROC=0.702,P=0.006;0.701,P=0.006;0.697,P=0.007)、类癌性心脏病(AUROC=0.896;0.887;0.923,P<0.001)和肝脏转移灶>30%(AUROC=0.827;0.807;0.849,P<0.001)相关,与其他传统预后因素无关。在饮食遵守情况为最佳或次佳的患者中,生物标志物水平相似。
在转移性中肠类癌患者中,Ou5HIAA 和 p5HIAA 可以作为 24u5HIAA 的更方便替代物。需要进行前瞻性、长期、重复剂量的研究。