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Baseline and on Treatment Biodistribution Variability of 18F-FLT Uptake in Patients With Advanced Melanoma: Brief Communication

  • Bernies van der Hiel*
  • , Else A Aalbersberg
  • , Alfons J M van den Eertwegh
  • , Jitha Fischer
  • , Ronald Boellaard
  • , Filip Y F L de Vos
  • , Marye J Boers-Sonderen
  • , Marcel P M Stokkel
  • , Linda J de Wit-van der Veen
  • , John B A G Haanen
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Purpose This prospective study evaluates the biodistribution of 18F-FLT PET in patients with advanced melanoma before and after treatment with BRAF/MEK inhibitors. Patients and Methods Eighteen BRAF-positive unresectable stage IIIc or IV melanoma patients referred for 18F-FLT PET/CT before (BL) and during (D14) BRAF/MEK inhibition were included. 18F-FLT accumulation in the liver, bone marrow, blood, and muscle was quantified. Results Baseline interpatient 18F-FLT uptake had a coefficient-of-variation between 17.5% and 21.5%. During treatment, liver uptake increased (SUVmeanBL = 4.86 ± 0.98, SUVmeanD14 = 6.31 ± 1.36, P < 0.001) and bone marrow uptake decreased (SUVmeanBL = 7.67 ± 1.65, SUVmeanD14 = 6.78 ± 1.19, P < 0.025). Both changes were unrelated to baseline metabolic tumor volume or tumor response. Conclusions To assess 18F-FLT PET, both liver and bone marrow uptake may be used as normal tissue references at baseline, but 18F-FLT biodistribution significantly changes in longitudinal response studies when treated with BRAF/MEK inhibitors.

Original languageEnglish
Pages (from-to)722-726
Number of pages5
JournalClinical Nuclear Medicine
Volume49
Issue number8
Early online date15 May 2024
DOIs
Publication statusPublished - 1 Aug 2024

Keywords

  • F-FLT
  • biodistribution
  • BRAF mutation
  • melanoma
  • targeted therapy

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