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An Orthotopic Sciatic Nerve Xenograft for Neurofibromatosis Type 1 Neurofibromas
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443
My burning issues in neuroendocrine tumours (NET)
Barbara Kiesewetter1,2, Markus Raderer1,2
11Department of Internal Medicine I, Division of Oncology, Medical University Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria.
Memo
|January 1, 2019
Summary
New treatments for advanced neuroendocrine tumors (NET) include somatostatin analogues (SSA) as first-line therapy and radionuclide therapy (PRRT) for midgut NET. Research is ongoing for NET G3 and immunotherapy.
Area of Science:
- Oncology
- Nuclear Medicine
- Pharmacology
Background:
- Advanced well-differentiated neuroendocrine tumors (NET) of gastroenteropancreatic (GEP) or lung origin have seen recent therapeutic advancements.
- Somatostatin analogues (SSA) are established as first-line treatment for GEP-NET, offering antiproliferative and symptomatic benefits.
- Everolimus, an mTOR inhibitor, is approved for progressive GEP- and lung-NET.
Purpose of the Study:
- To review current systemic treatment options for advanced neuroendocrine tumors.
- To discuss the role of somatostatin analogues (SSA), everolimus, and peptide receptor radionuclide therapy (PRRT).
- To highlight emerging areas of research including NET G3 and immunotherapy.
Main Methods:
- Review of pivotal clinical trials (PROMID, CLARINET) for SSA efficacy.
- Analysis of recent data on everolimus use in GEP- and lung-NET.
- Evaluation of current evidence and expert opinion on PRRT for midgut and non-midgut NET.
Main Results:
- SSA are the preferred first-line treatment for GEP-NET, providing antiproliferative and symptomatic relief.
- PRRT is a standard treatment for midgut-NET progressing on SSA, with ongoing discussion regarding its use in non-midgut NET.
- Optimal treatment strategies for NET G3 and the potential of immunotherapy are active areas of investigation.
Conclusions:
- Current systemic therapies for advanced NET include SSA, everolimus, and PRRT, with specific indications based on tumor origin and progression.
- PRRT is highly effective for midgut-NET and its application in other NET sites requires individualized multidisciplinary assessment.
- Future research directions focus on refining treatment for NET G3 and exploring the efficacy of immunotherapy in NET.
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