Interference With VIP to Distinguish Between Real and False VIPoma: National Study From the French Endocrine Tumors Group

Author:

Chevalier Benjamin12ORCID,Bonnet Delphine3ORCID,Lepage Come4ORCID,Perrier Marine5ORCID,Borson-Chazot Françoise6ORCID,Abeillon Juliette6ORCID,Delobel Jean Bernard7,Jannin Arnaud289ORCID,Hadoux Julien10ORCID,Haissaguere Magalie11ORCID,Lombard-Bohas Catherine12ORCID,Walter Thomas12ORCID,Chardon Laurence13ORCID

Affiliation:

1. Department of Nuclear Medicine, Lille University Hospital , Lille 59000 , France

2. School of Medicine, University of Lille , Lille 59000 , France

3. Department of Internal Medicine and Digestive Diseases, CHU Toulouse , Toulouse 31059 , France

4. Gastroenterology and Digestive Oncology, Hôpital Universitaire Le Bocage , Dijon 21079 , France

5. Université Reims Champagne-Ardenne, Department of Gastroenterology and Digestive Oncology, Reims University Hospital , 51092 Reims , France

6. Hospices Civils de Lyon, Hôpital Louis Pradel, Fédération d’Endocrinologie , Lyon 69500 , France

7. Hôpital Yves le Foll, Service de Gastroentérologie , Saint Brieuc 22000 , France

8. Department of Endocrinology, Diabetology and Metabolism, Lille University Hospital , Lille 59000 , France

9. CANTHER—Cancer—Heterogeneity Plasticity and Resistance to Therapies, University of Lille, UMR9020-U1277—CNRS, INSERM, CHU Lille , Lille 59000 , France

10. Department of Nuclear Medicine and Endocrine Oncology, Gustave Roussy Cancer Center , Villejuif 94800 , France

11. Endocrinology and Endocrine Oncology Department, Haut Leveque Hospital, University Hospital of Bordeaux , Bordeaux 33600 , France

12. Hospices Civils de Lyon, Hôpital Edouard Herriot, Service d’Oncologie , Lyon 69003 , France

13. Service de Biochimie, Groupement Hospitalier Est, Hospices Civils de Lyon , Bron 69500 , France

Abstract

Abstract Background Vasoactive intestinal peptide (VIP)-secreting tumors (VIPomas) are digestive neuroendocrine tumors in which the hormonal secretion is life-threatening. Biological confirmation is obtained by demonstrating an elevation in plasma VIP, usually using radioimmunoassay (RIA). In some cases, analytical interference is suspected. We developed 3 different techniques to detect interference in VIP RIA. Methods Three techniques were used: RIA after Sephadex column chromatography separation, RIA after polyethylene glycol precipitation, and 125I-labeled VIP binding test. We included patients with suspicion of false positive VIP (FPV) elevation. We then compared results with those of a group of “real,” proven VIPoma (RV). Results A total of 15 patients with FPV elevation and 9 RV patients were included. Interference was detected in all FPV patients vs none in RV. Clinical and biochemical parameters did not differ between FPV and RV patients, but VIP concentration in RIA was significantly higher in FPV patients than in RV patients (228 pmol/L vs 66 pmol/L, P = .038). Using a 125I-labeled VIP binding test, median proportion of radioactivity in the pellet was significantly higher in FPV than in RV patients (53% vs 13%, P < .0001). A 20.5% threshold presented excellent performances (sensitivity 100% [79.6-100], specificity 100% [70.1-100]). Conclusion We developed 3 different laboratory techniques to reveal interference in RIA VIP assays. The diagnostic performance of all 3 was excellent. These techniques must be employed in cases of discordance between VIP elevation and clinical presentation.

Publisher

The Endocrine Society

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