A distinct four-value blood signature of pyrexia under combination therapy of malignant melanoma with dabrafenib and trametinib evidenced by an algorithm-defined pyrexia score

PLoS One. 2022 Aug 25;17(8):e0273478. doi: 10.1371/journal.pone.0273478. eCollection 2022.

Abstract

Pyrexia is a frequent adverse event of BRAF/MEK-inhibitor combination therapy in patients with metastasized malignant melanoma (MM). The study's objective was to identify laboratory changes which might correlate with the appearance of pyrexia. Initially, data of 38 MM patients treated with dabrafenib plus trametinib, of which 14 patients developed pyrexia, were analysed retrospectively. Graphical visualization of time series of laboratory values suggested that a rise in C-reactive-protein, in parallel with a fall of leukocytes and thrombocytes, were indicative of pyrexia. Additionally, statistical analysis showed a significant correlation between lactate dehydrogenase (LDH) and pyrexia. An algorithm based on these observations was designed using a deductive and heuristic approach in order to calculate a pyrexia score (PS) for each laboratory assessment in treated patients. A second independent data set of 28 MM patients, 8 with pyrexia, was used for the validation of the algorithm. PS based on the four parameters CRP, LDH, leukocyte and thrombocyte numbers, were statistically significantly higher in pyrexia patients, differentiated between groups (F = 20.8; p = <0.0001) and showed a significant predictive value for the diagnosis of pyrexia (F = 6.24; p = 0.013). We provide first evidence that pyrexia in patients treated with BRAF/MEK-blockade can be identified by an algorithm that calculates a score.

MeSH terms

  • Algorithms
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Fever / chemically induced
  • Humans
  • Imidazoles
  • L-Lactate Dehydrogenase
  • Melanoma* / complications
  • Melanoma* / drug therapy
  • Melanoma* / pathology
  • Melanoma, Cutaneous Malignant
  • Mitogen-Activated Protein Kinase Kinases
  • Mutation
  • Oximes / adverse effects
  • Proto-Oncogene Proteins B-raf / genetics
  • Pyridones / adverse effects
  • Pyrimidinones / adverse effects
  • Retrospective Studies
  • Skin Neoplasms* / pathology

Substances

  • Imidazoles
  • Oximes
  • Pyridones
  • Pyrimidinones
  • trametinib
  • L-Lactate Dehydrogenase
  • Proto-Oncogene Proteins B-raf
  • Mitogen-Activated Protein Kinase Kinases
  • dabrafenib

Associated data

  • Dryad/10.5061/dryad.xpnvx0kjj

Grants and funding

The author received no specific funding for this work.