Can we rely on PET in the follow-up of advanced seminoma patients?

Urol Int. 2012;88(4):405-9. doi: 10.1159/000337056. Epub 2012 Apr 12.

Abstract

The management of residuals after completion of chemotherapy in advanced seminoma is controversial. It has been proposed that fluorodeoxyglucose-positron emission tomography (FDG-PET) can be used as a follow-up. In this study we investigated FDG-PET as a follow-up tool in advanced seminoma patients treated previously with chemotherapy or radiotherapy. Thirty-seven patients assigned to an advanced seminoma group based on CT and/or FDG-PET/CT and then treated with chemotherapy were included in the study. All these patients underwent FDG-PET/CT examination as a part of the follow-up scheme. Patients underwent retroperitoneal lymph node dissection (RPLND), radiotherapy, or were followed clinically by CT and/or PET/CT every 6 months. In 8 cases FDG-PET was positive: 5 of them underwent RPLND and 3 radiotherapy. Two patients with negative FDG-PET but positive CT also underwent RPLND. The remaining patients with negative FDG-PET results were followed up. FDG-PET/CT was false positive in one case >3 cm and one <3 cm, in 6 cases >3 cm it was true negative. While FDG-PET can find a viable tumor, there also is an important question of false positive results. It was clinically proven that a negative FDG-PET was correlated with stable disease, but we were unable to examine specimens in these cases.

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • False Positive Reactions
  • Fluorodeoxyglucose F18
  • Humans
  • Lymph Node Excision
  • Lymphatic Metastasis
  • Male
  • Multimodal Imaging*
  • Neoplasm, Residual
  • Poland
  • Positron-Emission Tomography*
  • Predictive Value of Tests
  • Radiopharmaceuticals
  • Reproducibility of Results
  • Retrospective Studies
  • Seminoma / diagnostic imaging*
  • Seminoma / drug therapy
  • Seminoma / radiotherapy
  • Seminoma / secondary
  • Seminoma / surgery
  • Seminoma / therapy*
  • Testicular Neoplasms / diagnostic imaging*
  • Testicular Neoplasms / drug therapy
  • Testicular Neoplasms / pathology
  • Testicular Neoplasms / radiotherapy
  • Testicular Neoplasms / surgery
  • Testicular Neoplasms / therapy*
  • Time Factors
  • Tomography, X-Ray Computed*
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18