AI Article Synopsis

  • Neuroendocrine neoplasms (NENs) are complex cancers with increasing prevalence, requiring a multidisciplinary approach to treatment due to diverse outcomes based on factors like tumor grade and location.
  • Large clinical trials have established important therapies for advanced small bowel neuroendocrine tumors (SBNETs), including somatostatin analogues and peptide receptor radionuclide therapy (PRRT), which have improved management strategies over the past decade.
  • The review covers the current systemic treatment options for advanced SBNETs, highlights new therapies like tyrosine kinase inhibitors, and addresses ongoing questions and guideline recommendations for palliative care.

Article Abstract

Neuroendocrine neoplasms (NENs) are a heterogeneous group of malignancies with rising incidence and prevalence. Outcome and therapy of small bowel neuroendocrine tumours (SBNETs) is variable, depending on the grade, differentiation, tumour burden, as well as the site of the tumour origin. Because of this, multidisciplinary approach is essential. Large randomized clinical trials, with somatostatin analogues (PROMID, CLARINET) or with peptide receptor radionuclide therapy (PRRT) with 177-lutetium (NETTER-1 trial) as well as the mammalian target of rapamycin inhibitor (mTOR) everolimus (RADIANT trials), represent milestones for the medical management of unresectable grade 1 and 2 SBNETS over the last decade. Novel therapies, such as tyrosine kinase inhibitors (TKI), are on the cutting edge. However, multiple unsolved questions remain. This review provides a comprehensive review of the main systemic therapeutic options for advanced SBNETs and discusses the latest guideline recommendations for palliative treatment.

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Source
http://dx.doi.org/10.1007/s11864-021-00863-yDOI Listing

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