Interdisciplinary evidence-based recommendations for the follow-up of early stage seminomatous testicular germ cell cancer patients

Strahlenther Onkol. 2011 Mar;187(3):158-66. doi: 10.1007/s00066-010-2227-x. Epub 2011 Feb 21.

Abstract

Purpose: To provide guidance regarding follow-up procedures after initial treatment of early stage testicular seminoma (clinical stages (CS) I-II A/B) based on current published evidence complemented by expert opinion.

Methods and material: An interdisciplinary, multinational working group consisting of urologists, medical oncologists, and radiation oncologists analyzed the published evidence regarding follow-up procedures in various stages of seminomatous and nonseminomatous testicular cancers. Focusing on radiooncological aspects, the recommendations contained herein are restricted to early stage seminoma (with radiotherapy being a standard treatment option). In particular, extent, frequency, and duration of imaging at follow-up were analyzed concerning relapse patterns, risk factors, and mode of relapse detection.

Results: Active surveillance, adjuvant carboplatin or radiotherapy are equally accepted options for CS I seminoma but they result in different relapse rates and patterns. Usually relapses occur within the first 2(-6) years. Routinely performed follow-up using computerized tomography (CT) after adjuvant treatment yield only low detection rates of recurrences. Therefore, there is no evidence to maintain routine examinations every 3-4 months. After treatment of stage IIA/B, detection rates of relapses or progression identified solely by routinely performed CT during follow-up are low.

Conclusion: Considering lifelong cure rates of up to 99% for patients treated for seminoma CS I-IIA/B, the negative impact of unnecessary ionizing radiation exposure has to be considered. The presented recommendations for various follow-up scenarios for early stage seminoma strongly promote the restrictive use of imaging procedures that utilize ionizing radiation (especially CT), due to its potential to induce secondary malignancies.

Publication types

  • Consensus Development Conference

MeSH terms

  • Antineoplastic Agents / administration & dosage
  • Carboplatin / administration & dosage
  • Chemotherapy, Adjuvant
  • Combined Modality Therapy
  • Cooperative Behavior*
  • Critical Pathways*
  • Disease Progression
  • Evidence-Based Medicine*
  • Follow-Up Studies
  • Humans
  • Image Processing, Computer-Assisted
  • Interdisciplinary Communication*
  • Male
  • Neoplasm Recurrence, Local / diagnosis*
  • Neoplasm Staging
  • Neoplasms, Radiation-Induced / etiology
  • Neoplasms, Second Primary / etiology
  • Patient Care Team*
  • Positron-Emission Tomography / adverse effects
  • Radiotherapy, Adjuvant
  • Seminoma / diagnosis
  • Seminoma / drug therapy
  • Seminoma / pathology*
  • Seminoma / radiotherapy*
  • Sensitivity and Specificity
  • Testicular Neoplasms / diagnosis
  • Testicular Neoplasms / drug therapy
  • Testicular Neoplasms / pathology*
  • Testicular Neoplasms / radiotherapy*
  • Tomography, X-Ray Computed / adverse effects
  • Ultrasonography

Substances

  • Antineoplastic Agents
  • Carboplatin