Durable complete response in a patient with leptomeningeal melanoma after treatment with dabrafenib, trametinib, and nivolumab

Pigment Cell Melanoma Res. 2024 Nov;37(6):801-807. doi: 10.1111/pcmr.13179. Epub 2024 Jul 3.

Abstract

Leptomeningeal disease (LMD) is a devastating complication of melanoma with a dismal prognosis. We present the case of a young man with stage IV BRAF V600E mutant melanoma with lung, lymph node, and brain metastases initially treated with ipilimumab and nivolumab, who subsequently developed LMD. Upon change to BRAF/MEK targeted therapy with nivolumab, a durable complete response was achieved and remains ongoing, off treatment, 7 years from diagnosis. Management of symptomatic LMD remains a critical unmet clinical challenge, with limited clinical trial data. This exceptional case is instructive, as the first published case of the use of the triplet, and the first durable response with therapy discontinuation, in melanoma LMD. The triple-drug regimen may be considered a viable option in fit patients. This case highlights the potential for long-term disease control and the critical and urgent need to develop clinical trials inclusive of patients with LMD to define the best treatment strategies.

Keywords: brain metastases; immunotherapy; leptomeningeal disease; melanoma; targeted therapy.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • Humans
  • Imidazoles* / pharmacology
  • Imidazoles* / therapeutic use
  • Male
  • Melanoma* / drug therapy
  • Melanoma* / pathology
  • Meningeal Neoplasms* / diagnostic imaging
  • Meningeal Neoplasms* / drug therapy
  • Meningeal Neoplasms* / pathology
  • Meningeal Neoplasms* / secondary
  • Nivolumab* / therapeutic use
  • Oximes* / therapeutic use
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf / genetics
  • Pyridones* / therapeutic use
  • Pyrimidinones* / pharmacology
  • Pyrimidinones* / therapeutic use

Substances

  • trametinib
  • Nivolumab
  • Pyrimidinones
  • dabrafenib
  • Oximes
  • Imidazoles
  • Pyridones
  • Proto-Oncogene Proteins B-raf