Clinical Trial · NCT05889312

Assessing Cancer Treatment Response to Therapy Using 18F-FSPG PET

Overview

Prospective single centre non-randomised exploratory observational study to measure changes in tumour cellular redox status with 18F-FSPG PET in stage 3 non-small cell lung cancer (NSCLC) and stage 3 and 4 head and neck squamous cell cancer (HNSCC) at baseline and during standard of care treatment, and to compare this with 18F-FDG PET/CT and RECIST 1.1 response at 12 weeks.

Sponsor

The Christie NHS Foundation Trust

Contacts

Gark Cook (CONTACT)

gary.cook@kcl.ac.uk

0207 188 8364

ClinicalTrials.gov

NCT05889312

Drug / Compound

FSPG

Isotope(s):
Target(s):
  • Cystine/glutamate antiporter
Ligand Class: Small Molecules

FDG

Isotope(s):
Target(s):
  • Glucose Transport
Ligand Class: Small Molecules

Eligibility

Inclusion

  • Willingness and ability to comply with scheduled study visits and tests
  • Confirmation of adequate function of all major organs and systems
  • Histologically confirmed HNSCC or NSCLC, who are treatment naïve and scheduled to commence standard of care treatment ((chemo)radiotherapy)

Exclusion

  • Pregnant or lactating women
  • Participants likely to require palliative radiotherapy within the first 12 weeks of treatment
  • Concomitant uncontrolled medical conditions
  • Prognosis less than 3 months
  • Previous anti-cancer treatment (only treatment naïve patients eligible for inclusion)