Skip to main navigation Skip to search Skip to main content

Imaging Proliferation of Stage IV Cutaneous Melanoma With 18F-FLT PET/CT A Potential Noninvasive Tool for Predicting Treatment Resistance to Targeted Therapy?

  • Bernies van der Hiel*
  • , Wouter V. Vogel
  • , Alfons J. M. van den Eertwegh
  • , Carmen A. Vlahu
  • , Filip Y. F. L. de Vos
  • , Marye J. Boers-Sonderen
  • , Marcel P. M. Stokkel
  • , Else A. Aalbersberg
  • , John B. A. G. Haanen
  • *Corresponding author for this work
  • Netherlands Cancer Institute
  • Amsterdam UMC - University of Amsterdam
  • Utrecht University
  • Radboud University Nijmegen

Research output: Contribution to journalArticleAcademicpeer-review

23 Downloads (Pure)

Abstract

Background: 18F-FLT PET/CT visualizes cellular proliferation and may correlate more directly with tumor aggressiveness and treatment response than 18F-FDG PET/CT in melanoma patients treated with BRAF/MEK inhibitors. We aimed to assess whether 18F-FLT PET/CT can predict early resistance to BRAF/MEK inhibitors in addition to current clinical tools in patients with BRAF-mutated metastatic melanoma. Patients and Methods: This explorative side study of the phase II multicenter REPOSIT trial included 19 patients with stage IV BRAF V600E/K-mutated cutaneous melanoma who underwent optional 18F-FLT PET/CT. 18F-FLT PET/CT was performed at baseline and after 2 weeks of treatment to evaluate baseline uptake and early changes in metabolic activity. 18F-FDG PET/CT was performed at baseline for comparison. Ki67 expression was assessed in metastatic tissue samples. Analyses included: (1) visual comparison of baseline 18F-FLT and 18F-FDG uptake, (2) correlation of 18F-FLT uptake with Ki-67, (3) semiquantitative analysis of baseline 18F-FLT uptake, and (4) evaluation of percentage change in 18F-FLT uptake after 2 weeks. Results: Patients with consistently lower 18F-FLT than 18F-FDG uptake in metastases had longer progression-free survival (PFS; median 9.6 months, range: 3.4 to 32.3) compared with those with equal/higher or heterogeneous 18F-FLT uptake (3.5 to 5.3 mo). Baseline 18F-FLT SULpeak did not correlate with Ki67 expression (P = 0.601), nor was Ki67 associated with PFS (P = 0.39). No significant PFS difference was observed between patients with baseline 18F-FLT SULpeak below or above the median (P = 0.601). However, a greater percentage decrease in 18F-FLT uptake at 2 weeks was associated with longer PFS (median: 13.9 vs 4.3 mo, P = 0.005). Conclusions: Baseline 18F-FLT uptake patterns relative to 18F-FDG, and early changes in 18F-FLT uptake, were associated with PFS in patients treated with BRAF/MEK inhibitors. These explorative findings suggest that 18F-FLT PET/CT may have predictive value, warranting confirmation in larger prospective studies.
Original languageEnglish
Article number10.1097/RLU.0000000000005999
Pages (from-to)e469-e476
JournalClinical nuclear medicine
Volume50
Issue number8
Early online date2025
DOIs
Publication statusPublished - 1 Aug 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • F-FLT
  • Ki67 expression
  • PET/CT
  • melanoma
  • targeted therapy

Fingerprint

Dive into the research topics of 'Imaging Proliferation of Stage IV Cutaneous Melanoma With 18F-FLT PET/CT A Potential Noninvasive Tool for Predicting Treatment Resistance to Targeted Therapy?'. Together they form a unique fingerprint.

Cite this