Skip to main content
Top
Published in: Endocrine Pathology 3/2007

01-09-2007

Prognostic Factors in Gastrointestinal Endocrine Tumors

Authors: Guido Rindi, Tiziana D’Adda, Elisabetta Froio, Giovanni Fellegara, Cesare Bordi

Published in: Endocrine Pathology | Issue 3/2007

Login to get access

Abstract

The gastrointestinal endocrine tumors are neoplastic lesions with often elusive malignant clinical behavior. The current WHO classification attempted to define a more effective approach by introducing the concepts of cell differentiation and site-specific malignancy, as well as specific criteria for carcinoma definition. WHO clinicopathological correlations embed the prognostic features: degree of cell differentiation, angioinvasion, proliferation fraction as assessed by mitotic index and Ki67, size, and functional activity. Other prognostic variables have been recognized, most of which related to specific biological features of neuroendocrine cancer cells. Nonetheless, the presence of liver or distant metastases are the prognostic variables ultimately determining the patients’ fate in terms of survival and/or therapy response. A recent proposal of tumor grading and tumor, nodes, and metastases (TNM) staging aims at a simple and practical system for patients stratification. Application of such proposal should be implemented in routine clinical practice.
Literature
1.
go back to reference Hanahan D. Heritable formation of pancreatic beta-cell tumours in transgenic mice expressing recombinant insulin/simian virus 40 oncogenes. Nature 315:115–22, 1985.PubMedCrossRef Hanahan D. Heritable formation of pancreatic beta-cell tumours in transgenic mice expressing recombinant insulin/simian virus 40 oncogenes. Nature 315:115–22, 1985.PubMedCrossRef
2.
go back to reference Murphy D, Bishop A, Rindi G, Murphy MN, Stamp GW, Hanson J, et al. Mice transgenic for a vasopressin-SV40 hybrid oncogene develop tumors of the endocrine pancreas and the anterior pituitary. A possible model for human multiple endocrine neoplasia type 1. Am J Pathol 129:552–66, 1987.PubMed Murphy D, Bishop A, Rindi G, Murphy MN, Stamp GW, Hanson J, et al. Mice transgenic for a vasopressin-SV40 hybrid oncogene develop tumors of the endocrine pancreas and the anterior pituitary. A possible model for human multiple endocrine neoplasia type 1. Am J Pathol 129:552–66, 1987.PubMed
3.
go back to reference Efrat S, Teitelman G, Anwar M, Ruggiero D, Hanahan D. Glucagon gene regulatory region directs oncoprotein expression to neurons and pancreatic alpha cells. Neuron 1:605–13, 1988.PubMedCrossRef Efrat S, Teitelman G, Anwar M, Ruggiero D, Hanahan D. Glucagon gene regulatory region directs oncoprotein expression to neurons and pancreatic alpha cells. Neuron 1:605–13, 1988.PubMedCrossRef
4.
go back to reference Rindi G, Bishop AE, Murphy D, Solcia E, Hogan B, Polak JM. A morphological analysis endocrine tumour genesis in pancreas and anterior pituitary of AVP/SV40 transgenic mice. Virchows Arch A Pathol Anat Histopathol 412:255–66, 1988.PubMedCrossRef Rindi G, Bishop AE, Murphy D, Solcia E, Hogan B, Polak JM. A morphological analysis endocrine tumour genesis in pancreas and anterior pituitary of AVP/SV40 transgenic mice. Virchows Arch A Pathol Anat Histopathol 412:255–66, 1988.PubMedCrossRef
5.
go back to reference Rindi G, Grant SG, Yiangou Y, Ghatei MA, Bloom SR, Bautch VL, et al. Development of neuroendocrine tumors in the gastrointestinal tract of transgenic mice. Heterogeneity of hormone expression. Am J Pathol 136:1349–63, 1990.PubMed Rindi G, Grant SG, Yiangou Y, Ghatei MA, Bloom SR, Bautch VL, et al. Development of neuroendocrine tumors in the gastrointestinal tract of transgenic mice. Heterogeneity of hormone expression. Am J Pathol 136:1349–63, 1990.PubMed
6.
go back to reference Rindi G, Efrat S, Ghatei MA, Bloom SR, Solcia E, Polak JM. Glucagonomas of transgenic mice express a wide range of general neuroendocrine markers and bioactive peptides. Virchows Arch A Pathol Anat Histopathol 419:115–29, 1991.PubMedCrossRef Rindi G, Efrat S, Ghatei MA, Bloom SR, Solcia E, Polak JM. Glucagonomas of transgenic mice express a wide range of general neuroendocrine markers and bioactive peptides. Virchows Arch A Pathol Anat Histopathol 419:115–29, 1991.PubMedCrossRef
7.
go back to reference Rindi G, Ratineau C, Ronco A, Candusso ME, Tsai M, Leiter AB. Targeted ablation of secretin-producing cells in transgenic mice reveals a common differentiation pathway with multiple enteroendocrine cell lineages in the small intestine. Development 126:4149–56, 1999.PubMed Rindi G, Ratineau C, Ronco A, Candusso ME, Tsai M, Leiter AB. Targeted ablation of secretin-producing cells in transgenic mice reveals a common differentiation pathway with multiple enteroendocrine cell lineages in the small intestine. Development 126:4149–56, 1999.PubMed
8.
go back to reference Crabtree JS, Scacheri PC, Ward JM, Garrett-Beal L, Emmert-Buck MR, Edgemon KA, et al. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci USA 98:1118–23, 2001.PubMedCrossRef Crabtree JS, Scacheri PC, Ward JM, Garrett-Beal L, Emmert-Buck MR, Edgemon KA, et al. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors. Proc Natl Acad Sci USA 98:1118–23, 2001.PubMedCrossRef
9.
go back to reference Crabtree JS, Scacheri PC, Ward JM, McNally SR, Swain GP, Montagna C, et al. Of mice and MEN1: insulinomas in a conditional mouse knockout. Mol Cell Biol 23:6075–85, 2003.PubMedCrossRef Crabtree JS, Scacheri PC, Ward JM, McNally SR, Swain GP, Montagna C, et al. Of mice and MEN1: insulinomas in a conditional mouse knockout. Mol Cell Biol 23:6075–85, 2003.PubMedCrossRef
10.
go back to reference Bertolino P, Tong WM, Galendo D, Wang ZQ, Zhang CX. Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1. Mol Endocrinol 17:1880–92, 2003.PubMedCrossRef Bertolino P, Tong WM, Galendo D, Wang ZQ, Zhang CX. Heterozygous Men1 mutant mice develop a range of endocrine tumors mimicking multiple endocrine neoplasia type 1. Mol Endocrinol 17:1880–92, 2003.PubMedCrossRef
11.
go back to reference Biondi CA, Gartside MG, Waring P, Loffler KA, Stark MS, Magnuson MA, et al. Conditional inactivation of the MEN1 gene leads to pancreatic and pituitary tumorigenesis but does not affect normal development of these tissues. Mol Cell Biol 24:3125–31, 2004.PubMedCrossRef Biondi CA, Gartside MG, Waring P, Loffler KA, Stark MS, Magnuson MA, et al. Conditional inactivation of the MEN1 gene leads to pancreatic and pituitary tumorigenesis but does not affect normal development of these tissues. Mol Cell Biol 24:3125–31, 2004.PubMedCrossRef
12.
go back to reference Pellegata NS, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Hofler H, et al. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci USA 103:15558–63, 2006.PubMedCrossRef Pellegata NS, Quintanilla-Martinez L, Siggelkow H, Samson E, Bink K, Hofler H, et al. Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans. Proc Natl Acad Sci USA 103:15558–63, 2006.PubMedCrossRef
13.
go back to reference Solcia E, Capella C, Fiocca R, Rindi G, Rosai J. Gastric argyrophil carcinoidosis in patients with Zollinger-Ellison syndrome due to type 1 multiple endocrine neoplasia. A newly recognized association. Am J Surg Pathol 14:503–13, 1990.PubMedCrossRef Solcia E, Capella C, Fiocca R, Rindi G, Rosai J. Gastric argyrophil carcinoidosis in patients with Zollinger-Ellison syndrome due to type 1 multiple endocrine neoplasia. A newly recognized association. Am J Surg Pathol 14:503–13, 1990.PubMedCrossRef
14.
go back to reference Vortmeyer AO, Huang S, Lubensky I, Zhuang Z. Non-islet origin of pancreatic islet cell tumors. J Clin Endocrinol Metab 89:1934–8, 2004.PubMedCrossRef Vortmeyer AO, Huang S, Lubensky I, Zhuang Z. Non-islet origin of pancreatic islet cell tumors. J Clin Endocrinol Metab 89:1934–8, 2004.PubMedCrossRef
15.
go back to reference Anlauf M, Perren A, Henopp T, Rudolph T, Garbrecht N, Schmitt A, et al. Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions. Gut 56:637–44, 2006.PubMedCrossRef Anlauf M, Perren A, Henopp T, Rudolph T, Garbrecht N, Schmitt A, et al. Allelic deletion of the MEN1 gene in duodenal gastrin and somatostatin cell neoplasms and their precursor lesions. Gut 56:637–44, 2006.PubMedCrossRef
16.
go back to reference Anlauf M, Schlenger R, Perren A, Bauersfeld J, Koch CA, Dralle H, et al. Microadenomatosis of the endocrine pancreas in patients with and without the multiple endocrine neoplasia type 1 syndrome. Am J Surg Pathol 30:560–74, 2006.PubMedCrossRef Anlauf M, Schlenger R, Perren A, Bauersfeld J, Koch CA, Dralle H, et al. Microadenomatosis of the endocrine pancreas in patients with and without the multiple endocrine neoplasia type 1 syndrome. Am J Surg Pathol 30:560–74, 2006.PubMedCrossRef
17.
go back to reference Perren A, Anlauf M, Henopp T, Rudolph T, Schmitt A, Raffel A, et al. Multiple endocrine neoplasia type 1 (MEN1): loss of one MEN1 allele in tumors and monohormonal endocrine cell clusters but not in islet hyperplasia of the pancreas. J Clin Endocrinol Metab 92:1118–28, 2007.PubMedCrossRef Perren A, Anlauf M, Henopp T, Rudolph T, Schmitt A, Raffel A, et al. Multiple endocrine neoplasia type 1 (MEN1): loss of one MEN1 allele in tumors and monohormonal endocrine cell clusters but not in islet hyperplasia of the pancreas. J Clin Endocrinol Metab 92:1118–28, 2007.PubMedCrossRef
18.
go back to reference Rindi G, Leiter AB, Kopin AS, Bordi C, Solcia E. The “normal” endocrine cell of the gut: changing concepts and new evidences. Ann N Y Acad Sci 1014:1–12, 2004.PubMedCrossRef Rindi G, Leiter AB, Kopin AS, Bordi C, Solcia E. The “normal” endocrine cell of the gut: changing concepts and new evidences. Ann N Y Acad Sci 1014:1–12, 2004.PubMedCrossRef
19.
go back to reference Lloyd RV, Wilson BS. Specific endocrine tissue marker defined by a monoclonal antibody. Science 222:628–30, 1983.PubMedCrossRef Lloyd RV, Wilson BS. Specific endocrine tissue marker defined by a monoclonal antibody. Science 222:628–30, 1983.PubMedCrossRef
20.
go back to reference Wiedenmann B, Franke WW. Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles. Cell 41:1017–28, 1985.PubMedCrossRef Wiedenmann B, Franke WW. Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles. Cell 41:1017–28, 1985.PubMedCrossRef
21.
go back to reference Bishop AE, Polak JM, Facer P, Ferri GL, Marangos PJ, Pearse AG. Neuron specific enolase: a common marker for the endocrine cells and innervation of the gut and pancreas. Gastroenterology 83:902–15, 1982.PubMed Bishop AE, Polak JM, Facer P, Ferri GL, Marangos PJ, Pearse AG. Neuron specific enolase: a common marker for the endocrine cells and innervation of the gut and pancreas. Gastroenterology 83:902–15, 1982.PubMed
22.
go back to reference Thompson RJ, Doran JF, Jackson P, Dhillon AP, Rode J. PGP9.5 a new marker for vertebrate neurons and neuroendocrine differentiation. Brain Res 278:224–8, 1983.PubMedCrossRef Thompson RJ, Doran JF, Jackson P, Dhillon AP, Rode J. PGP9.5 a new marker for vertebrate neurons and neuroendocrine differentiation. Brain Res 278:224–8, 1983.PubMedCrossRef
23.
go back to reference Lantuejoul S, Moro D, Michalides RJ, Brambilla C, Brambilla E. Neural cell adhesion molecules (NCAM) and NCAM-PSA expression in neuroendocrine lung tumors. Am J Surg Pathol 22:1267–76, 1998.PubMedCrossRef Lantuejoul S, Moro D, Michalides RJ, Brambilla C, Brambilla E. Neural cell adhesion molecules (NCAM) and NCAM-PSA expression in neuroendocrine lung tumors. Am J Surg Pathol 22:1267–76, 1998.PubMedCrossRef
24.
go back to reference Solcia E, Klöppel G, Sobin LH. Histological typing of endocrine tumours. New York: Springer-Verlag, 2000. Solcia E, Klöppel G, Sobin LH. Histological typing of endocrine tumours. New York: Springer-Verlag, 2000.
25.
go back to reference Hamilton SR, Aaltonen LA. World Health Organization classification of tumours, pathology and genetics of tumours of the digestive system. Lyon: IARC Press, 2000. Hamilton SR, Aaltonen LA. World Health Organization classification of tumours, pathology and genetics of tumours of the digestive system. Lyon: IARC Press, 2000.
26.
go back to reference DeLellis RA, Lloyd RV, Heitz PU, Eng C. World Health Organization classification of tumours, pathology and genetics of tumours of endocrine organs. Lyon: IARC Press, 2004. DeLellis RA, Lloyd RV, Heitz PU, Eng C. World Health Organization classification of tumours, pathology and genetics of tumours of endocrine organs. Lyon: IARC Press, 2004.
27.
go back to reference Rigaud G, Missiaglia E, Moore PS, Zamboni G, Falconi M, Talamini G, et al. High resolution allelotype of nonfunctional pancreatic endocrine tumors: identification of two molecular subgroups with clinical implications. Cancer Res 61:285–92, 2001.PubMed Rigaud G, Missiaglia E, Moore PS, Zamboni G, Falconi M, Talamini G, et al. High resolution allelotype of nonfunctional pancreatic endocrine tumors: identification of two molecular subgroups with clinical implications. Cancer Res 61:285–92, 2001.PubMed
28.
go back to reference Zhao JM, Moch H, Scheidweiler AF, Baer A, Schaffer AA, Speel EJM, et al. Genomic imbalances in the progression of endocrine pancreatic tumors. Genes Chromosomes Cancer 32:364–72, 2001.PubMedCrossRef Zhao JM, Moch H, Scheidweiler AF, Baer A, Schaffer AA, Speel EJM, et al. Genomic imbalances in the progression of endocrine pancreatic tumors. Genes Chromosomes Cancer 32:364–72, 2001.PubMedCrossRef
29.
go back to reference Jonkers YM, Claessen SM, Perren A, Schmid S, Komminoth P, Verhofstad AA, et al. Chromosomal instability predicts metastatic disease in patients with insulinomas. Endocr-Relat Cancer 12:435–47, 2005.PubMedCrossRef Jonkers YM, Claessen SM, Perren A, Schmid S, Komminoth P, Verhofstad AA, et al. Chromosomal instability predicts metastatic disease in patients with insulinomas. Endocr-Relat Cancer 12:435–47, 2005.PubMedCrossRef
30.
go back to reference Floridia G, Grilli G, Salvatore M, Pescucci C, Moore PS, Scarpa A, et al. Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumors. Cancer Genet Cytogenet 156:23–30, 2005.PubMedCrossRef Floridia G, Grilli G, Salvatore M, Pescucci C, Moore PS, Scarpa A, et al. Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumors. Cancer Genet Cytogenet 156:23–30, 2005.PubMedCrossRef
31.
go back to reference Pizzi S, Azzoni C, Bassi D, Bottarelli L, Milione M, Bordi C. Genetic alterations in poorly differentiated endocrine carcinomas of the gastrointestinal tract. Cancer 98:1273–82, 2003.PubMedCrossRef Pizzi S, Azzoni C, Bassi D, Bottarelli L, Milione M, Bordi C. Genetic alterations in poorly differentiated endocrine carcinomas of the gastrointestinal tract. Cancer 98:1273–82, 2003.PubMedCrossRef
32.
go back to reference Furlan D, Cerutti R, Uccella S, La Rosa S, Rigoli E, Genasetti A, et al. Different molecular profiles characterize well-differentiated endocrine tumors and poorly differentiated endocrine carcinomas of the gastroenteropancreatic tract. Clin Cancer Res 10:947–57, 2004.PubMedCrossRef Furlan D, Cerutti R, Uccella S, La Rosa S, Rigoli E, Genasetti A, et al. Different molecular profiles characterize well-differentiated endocrine tumors and poorly differentiated endocrine carcinomas of the gastroenteropancreatic tract. Clin Cancer Res 10:947–57, 2004.PubMedCrossRef
33.
go back to reference Rindi G, Azzoni C, La Rosa S, Klersy C, Paolotti D, Rappel S, et al. ECL cell tumor and poorly differentiated endocrine carcinoma of the stomach: prognostic evaluation by pathological analysis. Gastroenterology 116:532–42, 1999.PubMedCrossRef Rindi G, Azzoni C, La Rosa S, Klersy C, Paolotti D, Rappel S, et al. ECL cell tumor and poorly differentiated endocrine carcinoma of the stomach: prognostic evaluation by pathological analysis. Gastroenterology 116:532–42, 1999.PubMedCrossRef
34.
go back to reference Artale S, Giannetta L, Cerea G, Pedrazzoli P, Schiavetto I, Napolitano M, et al. Treatment of metastatic neuroendocrine carcinomas based on WHO classification. Anticancer Res 25:4463–9, 2005.PubMed Artale S, Giannetta L, Cerea G, Pedrazzoli P, Schiavetto I, Napolitano M, et al. Treatment of metastatic neuroendocrine carcinomas based on WHO classification. Anticancer Res 25:4463–9, 2005.PubMed
35.
go back to reference Bajetta E, Catena L, Procopio G, Bichisao E, Ferrari L, Della Torre S, et al. Is the new WHO classification of neuroendocrine tumours useful for selecting an appropriate treatment? Ann Oncol 16:1374–80, 2005.PubMedCrossRef Bajetta E, Catena L, Procopio G, Bichisao E, Ferrari L, Della Torre S, et al. Is the new WHO classification of neuroendocrine tumours useful for selecting an appropriate treatment? Ann Oncol 16:1374–80, 2005.PubMedCrossRef
36.
go back to reference Panzuto F, Nasoni S, Falconi M, Corleto VD, Capurso G, Cassetta S, et al. Prognostic factors and survival in endocrine tumor patients: comparison between gastrointestinal and pancreatic localization. Endocr-Relat Cancer 12:1083–92, 2005.PubMedCrossRef Panzuto F, Nasoni S, Falconi M, Corleto VD, Capurso G, Cassetta S, et al. Prognostic factors and survival in endocrine tumor patients: comparison between gastrointestinal and pancreatic localization. Endocr-Relat Cancer 12:1083–92, 2005.PubMedCrossRef
37.
go back to reference Ruszniewski P, Ish-Shalom S, Wymenga M, O’Toole D, Arnold R, Tomassetti P, et al. Rapid and sustained relief from the symptoms of carcinoid syndrome: results from an open 6-month study of the 28-day prolonged-release formulation of lanreotide. Neuroendocrinology 80:244–51, 2004.PubMedCrossRef Ruszniewski P, Ish-Shalom S, Wymenga M, O’Toole D, Arnold R, Tomassetti P, et al. Rapid and sustained relief from the symptoms of carcinoid syndrome: results from an open 6-month study of the 28-day prolonged-release formulation of lanreotide. Neuroendocrinology 80:244–51, 2004.PubMedCrossRef
38.
go back to reference Tomassetti P, Campana D, Piscitelli L, Casadei R, Nori F, Brocchi E, et al. Endocrine tumors of the ileum: factors correlated with survival. Neuroendocrinology 83:380–6, 2006.PubMedCrossRef Tomassetti P, Campana D, Piscitelli L, Casadei R, Nori F, Brocchi E, et al. Endocrine tumors of the ileum: factors correlated with survival. Neuroendocrinology 83:380–6, 2006.PubMedCrossRef
39.
go back to reference D’Adda T, Candidus S, Denk H, Bordi C, Hofler H. Gastric neuroendocrine neoplasms: tumour clonality and malignancy-associated large X-chromosomal deletions. J Pathol 189:394–401, 1999.PubMedCrossRef D’Adda T, Candidus S, Denk H, Bordi C, Hofler H. Gastric neuroendocrine neoplasms: tumour clonality and malignancy-associated large X-chromosomal deletions. J Pathol 189:394–401, 1999.PubMedCrossRef
40.
go back to reference Pizzi S, D’Adda T, Azzoni C, Rindi G, Grigolato P, Pasquali C, et al. Malignancy-associated allelic losses on the X-chromosome in foregut but not in midgut endocrine tumours. J Pathol 196:401–7, 2002.PubMedCrossRef Pizzi S, D’Adda T, Azzoni C, Rindi G, Grigolato P, Pasquali C, et al. Malignancy-associated allelic losses on the X-chromosome in foregut but not in midgut endocrine tumours. J Pathol 196:401–7, 2002.PubMedCrossRef
41.
go back to reference Missiaglia E, Moore PS, Williamson J, Lemoine NR, Falconi M, Zamboni G, et al. Sex chromosome anomalies in pancreatic endocrine tumors. Int J Cancer 98:532–8, 2002.PubMedCrossRef Missiaglia E, Moore PS, Williamson J, Lemoine NR, Falconi M, Zamboni G, et al. Sex chromosome anomalies in pancreatic endocrine tumors. Int J Cancer 98:532–8, 2002.PubMedCrossRef
42.
go back to reference Chen YJ, Vortmeyer A, Zhuang Z, Gibril F, Jensen RT. X-chromosome loss of heterozygosity frequently occurs in gastrinomas and is correlated with aggressive tumor growth. Cancer 100:1379–87, 2004.PubMedCrossRef Chen YJ, Vortmeyer A, Zhuang Z, Gibril F, Jensen RT. X-chromosome loss of heterozygosity frequently occurs in gastrinomas and is correlated with aggressive tumor growth. Cancer 100:1379–87, 2004.PubMedCrossRef
43.
go back to reference Couvelard A, Hu J, Steers G, O’Toole D, Sauvanet A, Belghiti J, et al. Identification of potential therapeutic targets by gene-expression profiling in pancreatic endocrine tumors. Gastroenterology 131:1597–610, 2006.PubMedCrossRef Couvelard A, Hu J, Steers G, O’Toole D, Sauvanet A, Belghiti J, et al. Identification of potential therapeutic targets by gene-expression profiling in pancreatic endocrine tumors. Gastroenterology 131:1597–610, 2006.PubMedCrossRef
44.
go back to reference Roldo C, Missiaglia E, Hagan JP, Falconi M, Capelli P, Bersani S, et al. MicroRNA expression abnormalities in pancreatic endocrine and acinar tumors are associated with distinctive pathologic features and clinical behavior. J Clin Oncol 24:4677–84, 2006.PubMedCrossRef Roldo C, Missiaglia E, Hagan JP, Falconi M, Capelli P, Bersani S, et al. MicroRNA expression abnormalities in pancreatic endocrine and acinar tumors are associated with distinctive pathologic features and clinical behavior. J Clin Oncol 24:4677–84, 2006.PubMedCrossRef
45.
go back to reference Butturini G, Bettini R, Missiaglia E, Mantovani W, Dalai I, Capelli P, et al. Predictive factors of efficacy of the somatostatin analogue octreotide as first line therapy for advanced pancreatic endocrine carcinoma. Endocr-Relat Cancer 13:1213–21, 2006.PubMedCrossRef Butturini G, Bettini R, Missiaglia E, Mantovani W, Dalai I, Capelli P, et al. Predictive factors of efficacy of the somatostatin analogue octreotide as first line therapy for advanced pancreatic endocrine carcinoma. Endocr-Relat Cancer 13:1213–21, 2006.PubMedCrossRef
46.
go back to reference Hochwald SN, Zee S, Conlon KC, Colleoni R, Louie O, Brennan MF, et al. Prognostic factors in pancreatic endocrine neoplasms: an analysis of 136 cases with a proposal for low-grade and intermediate-grade groups. J Clin Oncol 20:2633–42, 2002.PubMedCrossRef Hochwald SN, Zee S, Conlon KC, Colleoni R, Louie O, Brennan MF, et al. Prognostic factors in pancreatic endocrine neoplasms: an analysis of 136 cases with a proposal for low-grade and intermediate-grade groups. J Clin Oncol 20:2633–42, 2002.PubMedCrossRef
47.
go back to reference Van Eeden S, Quaedvlieg PF, Taal BG, Offerhaus GJ, Lamers CB, Van Velthuysen ML. Classification of low-grade neuroendocrine tumors of midgut and unknown origin. Hum Pathol 33:1126–32, 2002.PubMedCrossRef Van Eeden S, Quaedvlieg PF, Taal BG, Offerhaus GJ, Lamers CB, Van Velthuysen ML. Classification of low-grade neuroendocrine tumors of midgut and unknown origin. Hum Pathol 33:1126–32, 2002.PubMedCrossRef
48.
go back to reference Rindi G, Klöppel G, Ahlman H, Caplin M, Couvelard A, de Herder WW, et al. TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system. Virchows Arch 449:395–401, 2006.PubMedCrossRef Rindi G, Klöppel G, Ahlman H, Caplin M, Couvelard A, de Herder WW, et al. TNM staging of foregut (neuro)endocrine tumors: a consensus proposal including a grading system. Virchows Arch 449:395–401, 2006.PubMedCrossRef
49.
go back to reference Rindi G, de Herder WW, O’Toole D, Wiedenmann B. Consensus guidelines for the management of patients with digestive neuroendocrine tumors: why such guidelines and how we went about It. Neuroendocrinology 84:155–7, 2006.PubMedCrossRef Rindi G, de Herder WW, O’Toole D, Wiedenmann B. Consensus guidelines for the management of patients with digestive neuroendocrine tumors: why such guidelines and how we went about It. Neuroendocrinology 84:155–7, 2006.PubMedCrossRef
50.
go back to reference Panzuto F, Di Fonzo M, Iannicelli E, Sciuto R, Maini CL, Capurso G, et al. Long-term clinical outcome of somatostatin analogues for treatment of progressive, metastatic, well-differentiated entero-pancreatic endocrine carcinoma. Ann Oncol 17:461–6, 2006.PubMedCrossRef Panzuto F, Di Fonzo M, Iannicelli E, Sciuto R, Maini CL, Capurso G, et al. Long-term clinical outcome of somatostatin analogues for treatment of progressive, metastatic, well-differentiated entero-pancreatic endocrine carcinoma. Ann Oncol 17:461–6, 2006.PubMedCrossRef
51.
go back to reference Rossi G, Valli R, Bertolini F, Sighinolfi P, Losi L, Cavazza A, et al. Does mesoappendix infiltration predict a worse prognosis in incidental neuroendocrine tumors of the appendix? A clinicopathologic and immunohistochemical study of 15 cases. Am J Clin Pathol 120:706–11, 2003.PubMedCrossRef Rossi G, Valli R, Bertolini F, Sighinolfi P, Losi L, Cavazza A, et al. Does mesoappendix infiltration predict a worse prognosis in incidental neuroendocrine tumors of the appendix? A clinicopathologic and immunohistochemical study of 15 cases. Am J Clin Pathol 120:706–11, 2003.PubMedCrossRef
52.
go back to reference Stinner B, Rothmund M. Neuroendocrine tumours (carcinoids) of the appendix. Best Pract Res Clin Gastroenterol 19:729–38, 2005.PubMedCrossRef Stinner B, Rothmund M. Neuroendocrine tumours (carcinoids) of the appendix. Best Pract Res Clin Gastroenterol 19:729–38, 2005.PubMedCrossRef
53.
go back to reference Koura AN, Giacco GG, Curley SA, Skibber JM, Feig BW, Ellis LM. Carcinoid tumors of the rectum: effect of size, histopathology, and surgical treatment on metastasis free survival. Cancer 79:1294–8, 1997.PubMedCrossRef Koura AN, Giacco GG, Curley SA, Skibber JM, Feig BW, Ellis LM. Carcinoid tumors of the rectum: effect of size, histopathology, and surgical treatment on metastasis free survival. Cancer 79:1294–8, 1997.PubMedCrossRef
54.
go back to reference Schindl M, Niederle B, Hafner M, Teleky B, Langle F, Kaserer K, et al. Stage-dependent therapy of rectal carcinoid tumors. World J Surg 22:628–33; discussion 634, 1998.PubMedCrossRef Schindl M, Niederle B, Hafner M, Teleky B, Langle F, Kaserer K, et al. Stage-dependent therapy of rectal carcinoid tumors. World J Surg 22:628–33; discussion 634, 1998.PubMedCrossRef
55.
go back to reference Fahy BN, Tang LH, Klimstra D, Wong WD, Guillem JG, Paty PB, et al. Carcinoid of the Rectum Risk Stratification (CaRRS): a strategy for preoperative outcome assessment. Ann Surg Oncol 14:396–404, 2007.PubMedCrossRef Fahy BN, Tang LH, Klimstra D, Wong WD, Guillem JG, Paty PB, et al. Carcinoid of the Rectum Risk Stratification (CaRRS): a strategy for preoperative outcome assessment. Ann Surg Oncol 14:396–404, 2007.PubMedCrossRef
Metadata
Title
Prognostic Factors in Gastrointestinal Endocrine Tumors
Authors
Guido Rindi
Tiziana D’Adda
Elisabetta Froio
Giovanni Fellegara
Cesare Bordi
Publication date
01-09-2007
Publisher
Humana Press Inc
Published in
Endocrine Pathology / Issue 3/2007
Print ISSN: 1046-3976
Electronic ISSN: 1559-0097
DOI
https://doi.org/10.1007/s12022-007-0020-x

Other articles of this Issue 3/2007

Endocrine Pathology 3/2007 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine