Gastroenteropancreatic Neuroendocrine Tumors: Hormonal Treatment Updates

  • Simon Khagi Tufts Medical Center, Tufts University School of Medicine. Boston, MA, USA
  • Muhammad Wasif Saif Tufts Medical Center, Tufts University School of Medicine. Boston, MA, USA
Keywords: Carcinoid Tumor, everolimus, lanreotide, Neuroendocrine Tumors, Octreotide, pasireotide, Somatostatin

Abstract

Gastroenteropancreatic neuroendocrine tumors are a heterogeneous group of carcinomas that remain difficult to treat with conventional cytotoxic regimens. The 2014 American Society of Clinical Oncology (ASCO) Gastrointestinal Cancers Symposium brought us new insights into the management of gastroenteropancreatic neuroendocrine tumors. The focus of this review will serve to highlight specific Abstracts (#268 and #273) that help shed light on a novel, targeted means of treating gastroenteropancreatic neuroendocrine tumors.

Image: Carcinoid tumor of the small bowel (credit: Ed Uthman)

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References

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Carcinoid tumor of the small bowel (credit: Ed Uthman)
Published
2014-03-10
How to Cite
KhagiS., & SaifM. (2014). Gastroenteropancreatic Neuroendocrine Tumors: Hormonal Treatment Updates. JOP. Journal of the Pancreas, 15(2), 135-137. https://doi.org/10.6092/1590-8577/2287
Section
Highlights from the “2014 ASCO Gastrointestinal Cancers Symposium”. San Francisco, CA, USA. January 16-18, 2014