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Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas.

Publication ,  Journal Article
Tang, LH; Untch, BR; Reidy, DL; O'Reilly, E; Dhall, D; Jih, L; Basturk, O; Allen, PJ; Klimstra, DS
Published in: Clin Cancer Res
February 15, 2016

PURPOSE: Most well-differentiated neuroendocrine tumors (WD-NET) of the enteropancreatic system are low-intermediate grade (G1, G2). Elevated proliferation demonstrated by either a brisk mitotic rate (>20/10 high power fields) or high Ki-67 index (>20%) defines a group of aggressive neoplasms designated as high-grade (G3) neuroendocrine carcinoma (NEC). High-grade NEC is equated with poorly differentiated NEC (PD-NEC) and is associated with a dismal outcome. Progression of WD-NETs to a high-grade neuroendocrine neoplasm very rarely occurs and their clinicopathologic and molecular features need to be characterized. EXPERIMENTAL DESIGN: We investigated 31 cases of WD-NETs with evidence of a component of a high-grade neoplasm. The primary sites included pancreas, small bowel, bile duct, and rectum. Histopathology of the cases was retrospectively reviewed and selected IHC and gene mutation analyses performed. RESULTS: The high-grade component occurred either within the primary tumor (48%) or at metastatic sites (52%). The clinical presentation, radiographic features, biomarkers, and the genotype of these WD-NETs with high-grade component remained akin to those of G1-G2 WD-NETs. The median disease-specific survival (DSS) was 55 months (16-119 months), and 2-year and 5-year DSS was 88% and 49%, respectively-significantly better than that of a comparison group of true PD-NEC (DSS 11 months). CONCLUSIONS: Mixed grades can occur in WD-NETs, which are distinguished from PD-NECs by their unique phenotype, proliferative indices, and the genotype. This phenomenon of mixed grade in WD-NET provides additional evidence to the growing recognition that the current WHO G3 category contains both WD-NETs as well as PD-NECs.

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Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

February 15, 2016

Volume

22

Issue

4

Start / End Page

1011 / 1017

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Retrospective Studies
  • Proportional Hazards Models
  • Pancreatic Neoplasms
  • Oncology & Carcinogenesis
  • Neuroendocrine Tumors
  • Middle Aged
  • Male
  • Humans
  • Follow-Up Studies
 

Citation

APA
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MLA
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Tang, L. H., Untch, B. R., Reidy, D. L., O’Reilly, E., Dhall, D., Jih, L., … Klimstra, D. S. (2016). Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas. Clin Cancer Res, 22(4), 1011–1017. https://doi.org/10.1158/1078-0432.CCR-15-0548
Tang, Laura H., Brian R. Untch, Diane L. Reidy, Eileen O’Reilly, Deepti Dhall, Lily Jih, Olca Basturk, Peter J. Allen, and David S. Klimstra. “Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas.Clin Cancer Res 22, no. 4 (February 15, 2016): 1011–17. https://doi.org/10.1158/1078-0432.CCR-15-0548.
Tang, Laura H., et al. “Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas.Clin Cancer Res, vol. 22, no. 4, Feb. 2016, pp. 1011–17. Pubmed, doi:10.1158/1078-0432.CCR-15-0548.
Tang LH, Untch BR, Reidy DL, O’Reilly E, Dhall D, Jih L, Basturk O, Allen PJ, Klimstra DS. Well-Differentiated Neuroendocrine Tumors with a Morphologically Apparent High-Grade Component: A Pathway Distinct from Poorly Differentiated Neuroendocrine Carcinomas. Clin Cancer Res. 2016 Feb 15;22(4):1011–1017.

Published In

Clin Cancer Res

DOI

EISSN

1557-3265

Publication Date

February 15, 2016

Volume

22

Issue

4

Start / End Page

1011 / 1017

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Retrospective Studies
  • Proportional Hazards Models
  • Pancreatic Neoplasms
  • Oncology & Carcinogenesis
  • Neuroendocrine Tumors
  • Middle Aged
  • Male
  • Humans
  • Follow-Up Studies