Urothelial carcinoma with an NRF1-BRAF rearrangement and response to targeted therapy

Cold Spring Harb Mol Case Stud. 2019 Jun 3;5(3):a003848. doi: 10.1101/mcs.a003848. Print 2019 Jun.

Abstract

Although BRAF mutations are commonly identified in many solid tumors and the response of BRAF p.V600E-positive tumors to targeted therapy is well documented, BRAF rearrangements are less frequent and are predominantly found in low-grade glioma, melanoma, lung, colorectal, and thyroid carcinoma. Preclinical and clinical studies have demonstrated effectiveness of multiple therapies (RAF-targeted, ERK-targeted, or MEK-targeted) targeting BRAF-fusion harboring tumors. We report a rare NRF1-BRAF fusion with novel breakpoints, identified by next-generation sequencing-based assay, from a 69-year-old man with metastatic urothelial carcinoma (UC) of the renal pelvis and his initial clinical response to a second-generation MEK inhibitor, trametinib, before stopping the medication because of adverse side effects. The NRF1-BRAF fusion has only been reported in a single case of anaplastic pleomorphic xanthoastrocytoma, and BRAF rearrangement has never been reported in UC.

Keywords: neoplasm of the ureter; renal pelvic carcinoma.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Carcinoma / diagnostic imaging
  • Carcinoma / genetics*
  • Carcinoma / pathology
  • Humans
  • Kidney Neoplasms / diagnostic imaging
  • Kidney Neoplasms / genetics*
  • Kidney Neoplasms / pathology
  • Kidney Pelvis / diagnostic imaging
  • Kidney Pelvis / pathology
  • Liver / pathology
  • Male
  • Neoplasm Metastasis
  • Nuclear Respiratory Factor 1 / genetics*
  • Proto-Oncogene Proteins B-raf / genetics*

Substances

  • NRF1 protein, human
  • Nuclear Respiratory Factor 1
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf