Is FDG-PET suitable for evaluating neoadjuvant therapy in non-small cell lung cancer? Evidence with systematic review of the literature

J Surg Oncol. 2010 May 1;101(6):486-94. doi: 10.1002/jso.21525.

Abstract

Background: Neoadjuvant therapy response assessment is crucial in patients with non-small cell lung cancer (NSCLC). FDG-PET has emerged as a valuable tool for defining therapy response assessment in other tumours.

Aim: To systematically review publications appearing in the literature describing induction therapy response assessment with FDG-PET in NSCLC.

Methods: We performed a bibliographic search and selected only prospective studies in order to include the highest levels of evidence.

Results: Nine of 497 potentially relevant publications were selected. The ranges of sensitivity, specificity, positive predictive value and negative predictive value for primary tumour response assessment were 80-100%, 0-100%, 42.9-100%, and 66.7-100%, respectively. Pooling data for N2 restaging after neoadjuvant response the overall sensitivity was 63.8% (95% CI, 53.3-73.7%) and overall specificity was 85.3% (95% CI, 80.4-89.4%).

Conclusion: The results of the analysis do not support the use of FDG-PET as the only re-assessment tool for mediastinal lymph node evaluation for routine clinical use. FDG-PET seems to predict primary tumour response to induction therapy but it could not be shown by pooling analysis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Carcinoma, Non-Small-Cell Lung / diagnostic imaging*
  • Carcinoma, Non-Small-Cell Lung / therapy*
  • Fluorodeoxyglucose F18*
  • Lung Neoplasms / diagnostic imaging*
  • Lung Neoplasms / therapy*
  • Lymphatic Metastasis / diagnostic imaging
  • Neoadjuvant Therapy*
  • Positron-Emission Tomography*
  • Prospective Studies

Substances

  • Fluorodeoxyglucose F18