Aatur D Singhi 1 , Ta-Chiang Liu 2 , Justin L Roncaioli 3 , Dengfeng Cao 2 , Herbert J Zeh 4 , Amer H Zureikat 4 , Allan Tsung 4 , J Wallis Marsh 4 , Kenneth K Lee 4 , Melissa E Hogg 4 , Nathan Bahary 5 , Randall E Brand 5 , Kevin M McGrath 5 , Adam Slivka 5 , Kristi L Cressman 6 , Kimberly Fuhrer 6 , Roderick J O'Sullivan 3 . Show Affiliations »
Abstract
PURPOSE: Pancreatic neuroendocrine tumors (PanNET) are a heterogeneous group of neoplasms with increasing incidence and unpredictable behavior. Whole-exome sequencing has identified recurrent mutations in the genes DAXX and ATRX, which correlate with loss of protein expression and alternative lengthening of telomeres (ALT). Both ALT and DAXX/ATRX loss were initially reported to be associated with a favorable prognosis; however, recent studies suggest the contrary. Our aims were to assess the prevalence and prognostic significance of ALT and DAXX/ATRX in both primary and metastatic PanNETs. EXPERIMENTAL DESIGN: Telomere-specific FISH and DAXX/ATRX IHC was performed on a multi-institutional cohort of 321 patients with resected PanNET and 191 distant metastases from 52 patients. These results were correlated with clinicopathologic features, including disease-free survival (DFS) and disease-specific survival (DSS). RESULTS: The prevalence of ALT and DAXX/ATRX loss in resected PanNETs was 31% and 26%, respectively, and associated with larger tumor size, higher WHO grade, lymph node metastasis, and distant metastasis (P < 0.001). The 5-year DFS and 10-year DSS of patients with ALT-positive and DAXX/ATRX-negative PanNETs were 40% and 50%, respectively, as compared with 96% and 89%, respectively, for wild-type PanNETs. Among distant metastases, ALT and DAXX/ATRX loss was 67% and 52%, respectively, and only occurred in the setting of an ALT-positive and DAXX/ATRX-negative primary PanNET. By multivariate analysis, both ALT and DAXX/ATRX loss were negative, independent prognostic factors for DFS. CONCLUSIONS: ALT and DAXX/ATRX loss in PanNETs was associated with shorter DFS and DSS and likely plays a significant role in driving metastatic disease. Clin Cancer Res; 23(2); 600-9. ©2016 AACR. ©2016 American Association for Cancer Research.
PURPOSE: Pancreatic neuroendocrine tumors (PanNET) are a heterogeneous group of neoplasms with increasing incidence and unpredictable behavior. Whole-exome sequencing has identified recurrent mutations in the genes DAXX and ATRX , which correlate with loss of protein expression and alternative lengthening of telomeres (ALT). Both ALT and DAXX /ATRX loss were initially reported to be associated with a favorable prognosis; however, recent studies suggest the contrary. Our aims were to assess the prevalence and prognostic significance of ALT and DAXX /ATRX in both primary and metastatic PanNETs. EXPERIMENTAL DESIGN: Telomere-specific FISH and DAXX /ATRX IHC was performed on a multi-institutional cohort of 321 patients with resected PanNET and 191 distant metastases from 52 patients . These results were correlated with clinicopathologic features, including disease-free survival (DFS) and disease-specific survival (DSS ). RESULTS: The prevalence of ALT and DAXX /ATRX loss in resected PanNETs was 31% and 26%, respectively, and associated with larger tumor size, higher WHO grade, lymph node metastasis, and distant metastasis (P < 0.001). The 5-year DFS and 10-year DSS of patients with ALT-positive and DAXX /ATRX -negative PanNETs were 40% and 50%, respectively, as compared with 96% and 89%, respectively, for wild-type PanNETs. Among distant metastases , ALT and DAXX /ATRX loss was 67% and 52%, respectively, and only occurred in the setting of an ALT-positive and DAXX /ATRX -negative primary PanNET. By multivariate analysis, both ALT and DAXX /ATRX loss were negative, independent prognostic factors for DFS. CONCLUSIONS: ALT and DAXX /ATRX loss in PanNETs was associated with shorter DFS and DSS and likely plays a significant role in driving metastatic disease. Clin Cancer Res; 23(2); 600-9. ©2016 AACR. ©2016 American Association for Cancer Research.
Entities: Chemical
Disease
Gene
Species
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Year: 2016
PMID: 27407094 PMCID: PMC6560642 DOI: 10.1158/1078-0432.CCR-16-1113
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531