Gastroenteropancreatic neuroendocrine tumors: new insights in the diagnosis and therapy

被引:48
作者
Alexandraki, Krystallenia I. [1 ]
Kaltsas, Gregory [1 ]
机构
[1] Natl Univ Athens, Dept Pathophysiol, Athens 11527, Greece
关键词
Somatostatin analogs; Everolimus; Sunitinib; Temozolomide; SOMATOSTATIN RECEPTOR SCINTIGRAPHY; PANCREATIC ENDOCRINE CARCINOMAS; GASTROINTESTINAL STROMAL TUMOR; POSITRON-EMISSION-TOMOGRAPHY; NANETS CONSENSUS GUIDELINES; LUNG-CANCER CELLS; PHASE-II; CLINICAL-TRIALS; GA-68-DOTA-TYR(3)-OCTREOTIDE PET; RESPONSE EVALUATION;
D O I
10.1007/s12020-011-9562-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) are relatively rare and heterogenous malignancies. Recent advances in histopathological classification according to the anatomical site of origin, proliferation rate, and extend of the disease have created a valid and powerful tool for the prognostic stratification of GEP-NETs. Chromogranin A is still the best available marker used for the biochemical confirmation of these tumors, but new more sensitive markers are urgently required. Although scintigraphy with In-111-octreotide has widely been applied for the localization and staging of GEP-NETs, newer imaging modalities based on the functional characteristics of these tumors are evolving aiming not only to facilitate the diagnosis but also prognosis and evaluation of treatment. Somatostatin receptors are the primary therapeutic targets through somatostatin analogs and peptide receptor radionuclide therapy (PRRT) producing symptomatic, biochemical and to a lesser extent antiproliferative effects. Due to the relatively limited and erratic response to chemotherapy, new molecular targeted therapies exploiting some of the biological properties of GEP-NETs such as increased vascularity and inhibition of pathways involved in downstream signal transduction have evolved. Some of these therapies, the mTOR inhibitor everolimus and the tyrosine kinase inhibitor sunitinib, have been recently validated in phase III studies producing practice changing outcomes. In addition, two oral chemotherapeutic agents temozolomide and capecitabine, show promising effects and may replace streptozotocin-based regimens whereas combination therapies with the angiogenesis inhibitor bevacizumab are being investigated. Although progression free survival is used as a feasible primary end point due to the long survival of patients even in the presence of extensive disease prolongation of overall survival following the introduction of new therapies needs to be established.
引用
收藏
页码:40 / 52
页数:13
相关论文
共 107 条
[51]   High-resolution analysis of genetic alterations in small bowel carcinoid tumors reveals areas of recurrent amplification and loss [J].
Kulke, Matthew H. ;
Freed, Ellen ;
Chiang, Derek Y. ;
Philips, Juliet ;
Zahrieh, David ;
Glickman, Jonathan N. ;
Shivdasani, Ramesh A. .
GENES CHROMOSOMES & CANCER, 2008, 47 (07) :591-603
[52]   A prospective phase II study of 2-methoxyestradiol administered in combination with bevacizumab in patients with metastatic carcinoid tumors [J].
Kulke, Matthew H. ;
Chan, Jennifer A. ;
Meyerhardt, Jeffrey A. ;
Zhu, Andrew X. ;
Abrams, Thomas A. ;
Blaszkowsky, Lawrence S. ;
Regan, Eileen ;
Sidor, Carolyn ;
Fuchs, Charles S. .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (02) :293-300
[53]   Evolving Diagnostic and Treatment Strategies for Pancreatic Neuroendocrine Tumors [J].
Kulke, Matthew H. ;
Bendell, Johanna ;
Kvols, Larry ;
Picus, Joel ;
Pommier, Rodney ;
Yao, James .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2011, 4
[54]   Future Directions in the Treatment of Neuroendocrine Tumors: Consensus Report of the National Cancer Institute Neuroendocrine Tumor Clinical Trials Planning Meeting [J].
Kulke, Matthew H. ;
Siu, Lillian L. ;
Tepper, Joel E. ;
Fisher, George ;
Jaffe, Deborah ;
Haller, Daniel G. ;
Ellis, Lee M. ;
Benedetti, Jacqueline K. ;
Bergsland, Emily K. ;
Hobday, Timothy J. ;
Van Cutsem, Eric ;
Pingpank, James ;
Oberg, Kjell ;
Cohen, Steven J. ;
Posner, Mitchell C. ;
Yao, James C. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (07) :934-943
[55]   NANETS Treatment Guidelines Well-Differentiated Neuroendocrine Tumors of the Stomach and Pancreas [J].
Kulke, Matthew H. ;
Anthony, Lowell B. ;
Bushnell, David L. ;
de Herder, Wouter W. ;
Goldsmith, Stanley J. ;
Klimstra, David S. ;
Marx, Stephen J. ;
Pasieka, Janice L. ;
Pommier, Rodney F. ;
Yao, James C. ;
Jensen, Robert T. .
PANCREAS, 2010, 39 (06) :735-752
[56]   O6-Methylguanine DNA Methyltransferase Deficiency and Response to Temozolomide-Based Therapy in Patients with Neuroendocrine Tumors [J].
Kulke, Matthew H. ;
Hornick, Jason L. ;
Frauenhoffer, Christine ;
Hooshmand, Susanne ;
Ryan, David P. ;
Enzinger, Peter C. ;
Meyerhardt, Jeffrey A. ;
Clark, Jeffrey W. ;
Stuart, Keith ;
Fuchs, Charles S. ;
Redston, Mark S. .
CLINICAL CANCER RESEARCH, 2009, 15 (01) :338-345
[57]   Phase II study of temozolomide and thalidomide in patients with metastatic neuroendocrine tumors [J].
Kulke, MH ;
Stuart, K ;
Enzinger, PC ;
Ryan, DP ;
Clark, JW ;
Muzikansky, A ;
Vincitore, M ;
Michelini, A ;
Fuchs, CS .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (03) :401-406
[58]   Treatment with the radiolabeled somatostatin analog [177Lu-DOTA0, Tyr3] octreotate:: Toxicity, efficacy, and survival [J].
Kwekkeboom, Dik J. ;
de Herder, Wouter W. ;
Kam, Boen L. ;
van Eijck, Casper H. ;
van Essen, Martijn ;
Kooij, Peter P. ;
Feelders, Richard A. ;
van Aken, Maarten O. ;
Krenning, Eric P. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (13) :2124-2130
[59]   Somatostatin receptor-based imaging and therapy of gastroenteropancreatic neuroendocrine tumors [J].
Kwekkeboom, Dik J. ;
Kam, Boen L. ;
van Essen, Martijn ;
Teunissen, Jaap J. M. ;
van Eijck, Casper H. J. ;
Valkema, Roelf ;
de Jong, Marion ;
de Herder, Wouter W. ;
Krenning, Eric P. .
ENDOCRINE-RELATED CANCER, 2010, 17 (01) :R53-R73
[60]   Genetics of neuroendocrine and carcinoid tumours [J].
Leotlela, PD ;
Jauch, A ;
Holtgreve-Grez, H ;
Thakker, RV .
ENDOCRINE-RELATED CANCER, 2003, 10 (04) :437-450