Clinical Application of New Pheochromocytoma Markers: INSERM Pilot Study of the Specificity of Elevated Plasma EM66 Concentrations in Patients With Pheochromocytoma or Paraganglioma Compared to Patients With Essential Hypertension
Neuroendocrine tumors (NT) correspond to neoplasms that develop from endocrine and
neuroendocrine cells scattered throughout the body. They are characterized by the
occurrence, in their cytoplasm, of dense-core secretory vesicles containing hormones,
neuropeptides and acidic proteins such as granins. The diversity of NT (from hypophysis,
pancreas, adrenal, gastrointestinal tract) makes very difficult the identification and
evaluation of the different types of tumors by the diagnostic and prognostic tools currently
available. We have thus established a research program aimed at identifying new biological
markers for the detection, the prognosis and the follow-up of NT by seeking in tumor and
plasma samples of patients, granin-derived peptides. Our program was initiated on one type
of NT : pheochromocytoma. These neoplasms correspond to tumoral chromaffin cells mainly
originating from the adrenal medulla. It is considered that 10 % of pheochromocytoma
patients will develop metastases and, currently, except in the presence of metastases, there
are no means to predict malignancy of the tumor. We setup a radioimmunoassay of EM66 (a
secretogranin II-derived peptide) that allowed us to demonstrate that (i) plasma
concentrations of the peptide are significantly elevated in pheochromocytoma patients, (ii)
combined with other biological tests EM66 measurement increase the diagnostic sensitivity
for these neoplasms, (iii) after surgical removal of the tumor, plasma EM66 concentrations
rapidly return to basal level and, (iv) intra-tumoral EM66 concentrations are higher in
benign than in malignant pheochromocytomas (Yon et al., 2003, Guillemot et al., 2006). These
results reveal that EM66 constitutes a novel tool for the diagnosis, prognosis and follow-up
of pheochromocytoma. In the frame of a clinical use of an EM66 measurement test, it is
necessary to evaluate the specificity of this marker. For instance, renal deficiency,
hypergastrinemia, reduction of renal clearance, type A gastritis, Crohns disease, or
proton-pump inhibitory treatment, lead to increase plasma chromogranin A (CgA)
concentrations (false-positive cases). In addition, while hypertension account for one of
the symptoms of pheochromocytoma patients, in essential hypertensive patients, CgA levels
are higher than in normotensive individuals. The main objective of our clinical transfer
research project consists to study the specificity of the measurement of EM66 as a
diagnostic and prognostic marker of pheochromocytoma. This multicentric study will allow us
to compare plasma EM66 levels in pheochromocytoma patients with a cohort of essential
hypertensive patients. At the same time, in a long-range prospect, due to the lack of
malignancy markers for these tumors, we will investigate if plasma or tumor EM66 levels are
correlated to the differentiation status of pheochromocytomas, and if the expression level
of a set of genes that we identified by a transcriptomic approach developed in the
laboratory, is associated with the malignant status of the tumors. The stakes of this
transfer research, involving our laboratory and the Center for Clinical Investigations (CIC)
of Rouen and Lille, are to provide an easy and simple novel tool to practitioners and
anatomo-pathologists for the screening, the evaluation and the follow-up of patients with
neuroendocrine tumors.
Observational
Observational Model: Case Control, Time Perspective: Prospective
Plasma EM66
two years
No
Anne F Cailleux, MD
Principal Investigator
Rouen University Hospital
France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
2007/081/HP
NCT01022515
November 2008
December 2013
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