Extra-thoracic tumor burden but not thoracic tumor burden on 18F-FDG PET/CT is an independent prognostic biomarker for extensive-disease small cell lung cancer

  • Jong Ryool Oh
  • , Ji Hyoung Seo
  • , Chae Moon Hong
  • , Shin Young Jeong
  • , Sang Woo Lee
  • , Jaetae Lee
  • , Jung Joon Min
  • , Ho Chun Song
  • , Hee Seung Bom
  • , Young Chul Kim
  • , Byeong Cheol Ahn

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Purpose: The aim of this study was to evaluate the relationship and difference in prognostic significance between whole-body tumor burden, thoracic tumor burden, and extra-thoracic tumor burden on 18F-FDG PET/CT for patients with extensive-disease small cell lung cancer (ED-SCLC). Materials and methods: We performed a retrospective, two-center analysis for patients with ED-SCLC who underwent pretreatment 18F-FDG PET/CT. Metabolic tumor burden was estimated using whole-body metabolic tumor volume (MTVWB), thoracic metabolic tumor volume (MTVTRX), extra-thoracic metabolic tumor volume (MTVEXT), and the number of extra-thoracic tumor foci. Uni- and multivariate analyses were performed using various clinical factors and the metabolic indices. Results: A total of 91 patients were eligible for this study. MTVWB showed stronger correlation with MTVEXT than MTVTRX (r2=0.804 vs. 0.132, p<0.001, both), whereas no correlation was observed between MTVEXT and MTVTRX (r2=0.007, p=0.428). Patients with smaller MTVWB, MTVEXT, and extra-thoracic tumor foci showed longer survival than patients with larger MTVWB, MTVEXT, and extra-thoracic tumor foci, respectively, whereas the survival difference between patients with smaller MTVTRX and those with larger MTVTRX was not significant. Results of uni- and multivariate analyses showed that ECOG performance status (HR=2.31, p=0.015), initial chemotherapy cycles (HR=0.24, p<0.001), and the number of extra-thoracic tumor foci (HR=2.75, p<0.001) were independent prognostic factors for overall survival, and initial chemotherapy cycles (HR=0.25, p<0.001), and MTVEXT (HR=2.04, p=0.013) were independent prognostic factors for progression-free survival. Conclusion: These data provide evidence indicating that extra-thoracic tumor burden but not thoracic tumor burden is an independent prognostic biomarker for ED-SCLC, and support further exploration of novel treatment strategies targeting extra-thoracic tumor burden in order to improve the clinical outcomes of patients with ED-SCLC.

Original languageEnglish
Pages (from-to)218-225
Number of pages8
JournalLung Cancer
Volume81
Issue number2
DOIs
StatePublished - Aug 2013

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-FDG PET/CT
  • Biomarker
  • Extensive disease small cell lung cancer
  • Metabolic tumor volume
  • Oligometastases
  • Prognosis

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