Prolonged Response to Dabrafenib/Trametinib in Grade 3 Metastatic Pancreatic Neuroendocrine Tumor (NET G3) with BRAF

Benjamin E Ueberroth1, Christopher H Lieu2, Robert W Lentz2

  • 1Division of Medical Oncology, Department of Medicine, University of Colorado School of Medicine, 12801 E 17th Ave, MS 8117, Aurora, CO, 80045, USA. benjamin.ueberroth@cuanschutz.edu.

Abstract

Insights

BRAF-targeted therapy with dabrafenib/trametinib offers a new treatment option for metastatic pancreatic neuroendocrine tumors (pancNETs) with BRAF V600E mutations. This targeted approach shows promise, particularly for grade 3 pancNETs.

Area of Science:

  • Oncology
  • Molecular Diagnostics
  • Pharmacology

Background:

  • Metastatic pancreatic neuroendocrine tumors (pancNETs), especially grade 2 and 3, present treatment challenges due to multiple similar therapy options.
  • Limited data exists on targeted therapies for these rare tumors.

Purpose of the Study:

  • To present BRAF-targeted therapy as a viable treatment option for metastatic pancreatic neuroendocrine tumors grade 3 (pancNET G3).

Main Methods:

  • A case report detailing a patient with metastatic G3 pancNET (liver, lung, lymph node, scalp) harboring a BRAF V600E mutation.
  • Treatment administered was dabrafenib/trametinib (D/T).

Main Results:

  • The patient achieved an ongoing partial response across all metastatic sites for nearly 15 months.
  • Minimal side effects were observed with the D/T therapy.

Conclusions:

  • Dabrafenib/trametinib therapy is a novel treatment option for BRAF-mutated metastatic pancNETs.
  • This therapy should be considered a first-line option for G3 pancNETs.
  • Testing for actionable mutations at diagnosis or progression is crucial for identifying new therapeutic strategies.