Recent chemotherapy reduces the maximum-standardized uptake value of 18F-fluoro-deoxyglucose positron emission tomography in colorectal cancer

Gut Liver. 2014 May;8(3):254-64. doi: 10.5009/gnl.2014.8.3.254.

Abstract

Background/aims: The aim of this study was to evaluate the influence of recent chemotherapy on the patterns of the maximum-standardized uptake value (M-SUV) and sensitivity of (18)F-fluoro-deoxyglucose positron emission tomography/computed tomography ((18)F-FDG-PET/CT) in colorectal cancer.

Methods: We retrospectively analyzed the FDG-PET/CT of 509 patients who underwent surgery for colorectal cancer. Subgroup analysis was performed according to chemotherapy status; 401 patients were not treated with chemotherapy and 108 patients were treated with chemotherapy within 6 months prior to surgery. Pathologic analysis of the surgical specimen was used as the gold standard.

Results: The M-SUV was significantly lower in patients treated with chemotherapy than in those not treated with chemotherapy in pathologically confirmed same stages of disease. The difference in the sensitivity of the M-SUV according to chemotherapy status was greatest using a cutoff M-SUV value of 6.4 (p<0.001). The longest diameter of the primary tumor was the most important factor that correlated with M-SUV of the primary tumor irrespective of the chemotherapy effect (p<0.001). The M-SUV of the primary tumor was not an independent predictor of lymph node metastasis in colorectal cancer.

Conclusions: The results indicate that the M-SUV of FDG-PET/CT should be interpreted in the context of concurrent chemotherapy.

Keywords: Colorectal neoplasms; Drug therapy; FDG-PET/CT.

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects*
  • Chemoradiotherapy, Adjuvant / adverse effects
  • Chemotherapy, Adjuvant / adverse effects
  • Colorectal Neoplasms / diagnostic imaging*
  • Colorectal Neoplasms / drug therapy
  • Colorectal Neoplasms / pathology
  • Female
  • Fluorodeoxyglucose F18 / pharmacology*
  • Humans
  • Male
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Positron-Emission Tomography / methods
  • Radiopharmaceuticals / pharmacology*
  • Retrospective Studies

Substances

  • Antineoplastic Agents
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18