Grading of Neuroendocrine Carcinomas: Correlation of 68Ga-PET/CT Scan with Tissue Biomarkers

被引:10
作者
Liverani, Chiara [1 ]
Bongiovanni, Alberto [1 ]
Mercatali, Laura [1 ]
Foca, Flavia [2 ]
Pieri, Federica [1 ]
De Vita, Alessandro [1 ]
Spadazzi, Chiara [1 ]
Miserocchi, Giacomo [1 ]
Recine, Federica [1 ]
Riva, Nada [1 ]
Nicolini, Silvia [3 ]
Severi, Stefano [3 ]
Martinelli, Giovanni [4 ]
Ibrahim, Toni [1 ]
机构
[1] IRCCS, Ist Sci Romagnolo Studio & Cura Tumori IRST, Osteoncol & Rare Tumors Ctr, Meldola, Italy
[2] IRCCS, Ist Sci Romagnolo Studio & Cura Tumori IRST, Unit Biostat & Clin Trials, Meldola, Italy
[3] IRCCS, Ist Sci Romagnolo Studio & Cura Tumori IRST, Nucl Med Unit, Meldola, Italy
[4] IRCCS, Ist Sci Romagnolo Studio & Cura Tumori IRST, Sci Directorate, Meldola, Italy
关键词
PROGNOSTIC-FACTORS; SMALL-CELL; TUMORS; WELL; NEOPLASMS; PET/CT; G3; CLASSIFICATION; EXPRESSION; MANAGEMENT;
D O I
10.1155/2018/6878409
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
There is a growing need for more accurate biomarkers to facilitate the diagnosis and prognosis of patients with grade (G) 3 neuroendocrine carcinomas (NECs). In particular, the discrimination between well-differentiated neuroendocrine carcinomas (WD-NECs) and poorly differentiated neuroendocrine carcinomas (PD-NECs) is still an unmet need. We previously showed that (68)Gallium-(Ga-68-) PET/CT positivity is a prognostic factor in patients with gastroenteropancreatic (GEP) G3 NECs, correlating with a better outcome in terms of overall survival. Here, we hypothesize that Ga-68-PET/CT could help to discriminate between WD-NECs and PD-NECs, adding complementary information to that obtained from morphologic and biologic factors. A retrospective, single-institution study was performed on 11 patients with histologically confirmed, measurable G3 large- or small-cell GEP-NECs according to the 2017 WHO classification. The staging procedures included a Ga-68-PET/CT scan. Results of Ga-68-PET/CT were correlated in univariate analysis with loss of tissue immunohistochemical expression of DAXX/ATRX or RB1 frequently associated with WD-NECs or PD-NECs, respectively. None of the patients with positive Ga-68-PET/CT showed loss of RB1 expression, whereas among those (n=6) with negative Ga-68-PET/CT, 4 showed loss of expression. A trend towards a correlation between loss of RB1 expression and negative Ga-68-PET/CT was observed. Our preliminary data support the hypothesis that PD-NECs carrying RB1 mutation and loss of its expression may be associated with negative Ga-68-PET/CT. If confirmed in a larger clinical trial, Ga-68-PET/CT would help in the stratification of G3 NECs.
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页数:8
相关论文
共 34 条
[1]  
Adams S, 1998, EUR J NUCL MED, V25, P79
[2]   ISL1 expression is not restricted to pancreatic well-differentiated neuroendocrine neoplasms, but is also commonly found in well and poorly differentiated neuroendocrine neoplasms of extrapancreatic origin [J].
Agaimy, Abbas ;
Erlenbach-Wuensch, Katharina ;
Konukiewitz, Bjoern ;
Schmitt, Anja M. ;
Rieker, Ralf J. ;
Vieth, Michael ;
Kiesewetter, Franklin ;
Hartmann, Arndt ;
Zamboni, Giuseppe ;
Perren, Aurel ;
Kloeppel, Guenter .
MODERN PATHOLOGY, 2013, 26 (07) :995-1003
[3]   Are radiogallium-labelled DOTA-conjugated somatostatin analogues superior to those labelled with other radiometals? [J].
Antunes, P. ;
Ginj, M. ;
Zhang, H. ;
Waser, B. ;
Baum, R. P. ;
Reubi, J. C. ;
Maecke, H. .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2007, 34 (07) :982-993
[4]   The High-grade (WHO G3) Pancreatic Neuroendocrine Tumor Category Is Morphologically and Biologically Heterogenous and Includes Both Well Differentiated and Poorly Differentiated Neoplasms [J].
Basturk, Olca ;
Yang, Zhaohai ;
Tang, Laura H. ;
Hruban, Ralph H. ;
Adsay, Volkan ;
McCall, Chad M. ;
Krasinskas, Alyssa M. ;
Jang, Kee-Taek ;
Frankel, Wendy L. ;
Balci, Serdar ;
Sigel, Carlie ;
Klimstra, David S. .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2015, 39 (05) :683-690
[5]   The Status of Neuroendocrine Tumor Imaging: From Darkness to Light? [J].
Bodei, Lisa ;
Sundin, Anders ;
Kidd, Mark ;
Prasad, Vikas ;
Modlin, Irvin M. .
NEUROENDOCRINOLOGY, 2015, 101 (01) :1-17
[6]   First-line chemotherapy in patients with metastatic gastroenteropancreatic neuroendocrine carcinoma [J].
Bongiovanni, Alberto ;
Riva, Nada ;
Ricci, Marianna ;
Liverani, Chiara ;
La Manna, Federico ;
De Vita, Alessandro ;
Foca, Flavia ;
Mercatali, Laura ;
Severi, Stefano ;
Amadori, Dino ;
Ibrahim, Toni .
ONCOTARGETS AND THERAPY, 2015, 8 :3613-3619
[7]   Somatostatin receptor biology in neuroendocrine and pituitary tumours: part 1-molecular pathways [J].
Cakir, Mehtap ;
Dworakowska, Dorota ;
Grossman, Ashley .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2010, 14 (11) :2570-2584
[8]   Prediction of Pancreatic Neuroendocrine Tumor Grade Based on CT Features and Texture Analysis [J].
Canellas, Rodrigo ;
Burk, Kristine S. ;
Parakh, Anushri ;
Sahani, Dushyant V. .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2018, 210 (02) :341-346
[9]   Role of PD-L1 expression as a biomarker for GEP neuroendocrine neoplasm grading [J].
Cavalcanti, Elisabetta ;
Armentano, Raffaele ;
Valentini, Anna Maria ;
Chieppa, Marcello ;
Caruso, Maria Lucia .
CELL DEATH & DISEASE, 2017, 8 :e3004-e3004
[10]  
Cescato R, 2006, J NUCL MED, V47, P502