Alternative use of BRAF inhibitors in patients with metastatic melanoma unable to swallow pills

J Oncol Pharm Pract. 2021 Jun;27(4):996-999. doi: 10.1177/1078155220953877. Epub 2020 Sep 2.

Abstract

Introduction: BRAF and MEK inhibitors have been approved for use in metastatic melanoma therapies. All of them are administered as oral capsules or pills. We report two cases treated applying an alternative method of vemurafenib or debrafenib-trametinib administration in patients unable to swallow.

Case report: The first case involved a 38-year-old man who was referred to a dermatologist for dysphagia and anorexia. After a computerized tomography (CT) scan it was concluded that the dysphagia was due to compression by mediastinal metastasis in a context of metastatic BRAF mutant melanoma. The second case involved a 35-year-old man who was diagnosed in March 2017 with melanoma of the back of the hand. Several months later a positron emission tomography (PET)/CT scan was performed. It revealed multiple disseminated metastasis.Management & Outcome: The first patient presented total dysphagia and was unable to swallow pills. It was decided to dissolve vemurafenib in order to facilitate administration. Dysphagia was improved 48 hours later, and oral feeding was reintroduced. Due to severe tablet phobia, the second patient was unable to swallow pills. Dabrafenib capsules were emptied and trametinib pills were grinded. One month later, we noted improved health associated with reduction of the metastases.

Discussion: Our study highlights the possibility of crushing or dissolving BRAF and MEK inhibitors in metastatic melanoma patients for whom it is impossible to swallow pills, eliciting a response and achieving significant if temporary clinical benefit.

Keywords: Melanoma; anti-BRAF therapy; anti-MEK therapy; benefit.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / metabolism
  • Deglutition Disorders / diagnostic imaging
  • Deglutition Disorders / drug therapy*
  • Humans
  • Imidazoles / administration & dosage
  • Imidazoles / metabolism
  • Male
  • Melanoma / diagnostic imaging
  • Melanoma / drug therapy*
  • Oximes / administration & dosage
  • Oximes / metabolism
  • Protein Kinase Inhibitors / administration & dosage*
  • Protein Kinase Inhibitors / metabolism
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors*
  • Proto-Oncogene Proteins B-raf / metabolism
  • Pyridones / administration & dosage
  • Pyridones / metabolism
  • Pyrimidinones / administration & dosage
  • Pyrimidinones / metabolism
  • Skin Neoplasms / diagnostic imaging
  • Skin Neoplasms / drug therapy*
  • Vemurafenib / administration & dosage
  • Vemurafenib / metabolism

Substances

  • Antineoplastic Agents
  • Imidazoles
  • Oximes
  • Protein Kinase Inhibitors
  • Pyridones
  • Pyrimidinones
  • Vemurafenib
  • trametinib
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • dabrafenib