Predictive factors of response to mTOR inhibitors in neuroendocrine tumours

Maria Chiara Zatelli1, Giuseppe Fanciulli2, Pasqualino Malandrino2

  • 1Section of Endocrinology and Internal MedicineDepartment of Medical Sciences, University of Ferrara, Via Aldo Moro 8, 44124 Cona - Ferrara, ItalyNeuroendocrine Tumours UnitDepartment of Clinical and Experimental Medicine, University of Sassari - AOU Sassari, Sassari, ItalyEndocrinology UnitGaribaldi Nesima Medical Center, Catania, ItalyDepartment of Clinical Medicine and Surgery"Federico II" University of Naples, Naples, ItalyThyroid and Parathyroid Surgery UnitIstituto Nazionale per lo studio e la cura dei tumori "Fondazione G. Pascale" - IRCCS, Naples, Italy ztlmch@unife.it.

Endocrine-Related Cancer
|December 16, 2015
PubMed

Insights

Identifying biomarkers for mTOR inhibitors (rapalogs) is crucial for effectively treating neuroendocrine tumors (NETs). This review explores tissue, circulating, and imaging markers to predict patient response to rapalog therapy.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Neuroendocrine tumors (NETs) treatment has advanced with drugs like somatostatin analogs, tyrosine kinase inhibitors, and mTOR inhibitors (rapalogs).
  • Rapalogs are approved for advanced pancreatic NETs and show efficacy in various NET types, though treatment resistance can occur.
  • Predicting which patients will benefit from rapalogs is essential for personalized treatment and efficient healthcare resource allocation.

Purpose of the Study:

  • To review current data on predictive markers for rapalog efficacy in neuroendocrine tumors (NETs).
  • To identify potential tissue, circulating, and imaging biomarkers for tailored patient management.

Main Methods:

  • Literature review of studies investigating predictive markers for rapalog treatment in NETs.
  • Analysis of data on tissue-based, blood-based (circulating), and imaging markers.

Main Results:

  • Various markers are under investigation for their potential to predict response to rapalog therapy in NETs.
  • Identifying these markers could help select patients likely to benefit, avoiding ineffective treatments.

Conclusions:

  • Predictive markers are vital for optimizing rapalog treatment selection in NET patients.
  • Further research into tissue, circulating, and imaging markers will enhance personalized medicine approaches for NETs.

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