TY - JOUR
T1 - Low microvessel density is an unfavorable histoprognostic factor in pancreatic endocrine tumors
AU - Marion-Audibert, Anne Marie
AU - Barel, Cécile
AU - Gouysse, Géraldine
AU - Dumortier, Jérôme
AU - Pilleul, Frank
AU - Pourreyron, Céline
AU - Hervieu, Valérie
AU - Poncet, Gilles
AU - Lombard-Bohas, Catherine
AU - Chayvialle, Jean Alain
AU - Partensky, Christian
AU - Scoazec, Jean Yves
N1 - Funding Information:
Supported by grants from Ligue contre le Cancer (Comité de Saône et Loire), Région Rhône-Alpes (Programme Emergence), Société Nationale Française de Gastro-Entérologie (Fonds de Recherche), and Fondation pour la Recherche Médicale. Anne-Marie Marion-Audibert is a recipient of a grant from Fondation de France. Géraldine Gouysse was supported by a grant from Hospices Civils de Lyon (Appel d’Offres Recherche Clinique 1997).
PY - 2003/10/1
Y1 - 2003/10/1
N2 - Background & Aims: In many malignant tumors, intratumoral microvascular density (MVD) has been suggested to be a prognostic parameter. We aimed to provide a quantitative evaluation of intratumoral microvascular density in a large series of resected endocrine tumors of the pancreas and to evaluate the potential prognostic significance of this parameter. Methods: Eighty-two tumors from 77 patients have been studied. MVD was evaluated by 2 observers after CD34 immunostaining and correlated with the following parameters: WHO classification, hormonal profile, tumor size, vascular endothelial growth factor expression, occurrence of metastasis, duration of survival. Results: MVD ranged from 5 to 92 vessels/field. MVD was significantly higher in well-differentiated benign endocrine tumors than in tumors of uncertain behavior and in carcinomas. No close correlation was found between MVD and the hormonal profile. MVD was significantly higher in tumors characterized by the following histoprognostic parameters: size <2 cm, proliferation index <2%, no evidence of metastasis. No close correlation was observed between MVD and VEGF expression. Finally, a MVD <30 vessels/field was associated with the occurrence of metastasis in tumors <2 cm and/or with a proliferation index <2% and with a significantly shorter survival after surgery. Conclusions: The quantitative analysis of microvessel density in pancreatic endocrine tumors may identify patients who, despite favorable conventional histoprognostic factors, are at risk of unfavorable evolution.
AB - Background & Aims: In many malignant tumors, intratumoral microvascular density (MVD) has been suggested to be a prognostic parameter. We aimed to provide a quantitative evaluation of intratumoral microvascular density in a large series of resected endocrine tumors of the pancreas and to evaluate the potential prognostic significance of this parameter. Methods: Eighty-two tumors from 77 patients have been studied. MVD was evaluated by 2 observers after CD34 immunostaining and correlated with the following parameters: WHO classification, hormonal profile, tumor size, vascular endothelial growth factor expression, occurrence of metastasis, duration of survival. Results: MVD ranged from 5 to 92 vessels/field. MVD was significantly higher in well-differentiated benign endocrine tumors than in tumors of uncertain behavior and in carcinomas. No close correlation was found between MVD and the hormonal profile. MVD was significantly higher in tumors characterized by the following histoprognostic parameters: size <2 cm, proliferation index <2%, no evidence of metastasis. No close correlation was observed between MVD and VEGF expression. Finally, a MVD <30 vessels/field was associated with the occurrence of metastasis in tumors <2 cm and/or with a proliferation index <2% and with a significantly shorter survival after surgery. Conclusions: The quantitative analysis of microvessel density in pancreatic endocrine tumors may identify patients who, despite favorable conventional histoprognostic factors, are at risk of unfavorable evolution.
UR - http://www.scopus.com/inward/record.url?scp=0141594629&partnerID=8YFLogxK
U2 - 10.1016/S0016-5085(03)01198-3
DO - 10.1016/S0016-5085(03)01198-3
M3 - Article
C2 - 14517793
AN - SCOPUS:0141594629
SN - 0016-5085
VL - 125
SP - 1094
EP - 1104
JO - Gastroenterology
JF - Gastroenterology
IS - 4
ER -