2017 GPOH Guidelines for Diagnosis and Treatment of Patients with Neuroblastic Tumors

Klin Padiatr. 2017 May;229(3):147-167. doi: 10.1055/s-0043-103086. Epub 2017 May 30.

Abstract

The clinical course of neuroblastoma is more heterogeneous than any other malignant disease. Most low-risk patients experience regression after limited or even no chemotherapy. However, more than half of high-risk patients die from disease despite intensive multimodal treatment. Precise patient characterization at diagnosis is key for risk-adapted treatment. The guidelines presented here incorporate results from national and international clinical trials to produce recommendations for diagnosing and treating neuroblastoma patients in German hospitals outside of clinical trials.

Publication types

  • Practice Guideline

MeSH terms

  • Child
  • Clinical Trials as Topic
  • Combined Modality Therapy
  • Ganglioneuroma / diagnosis*
  • Ganglioneuroma / mortality
  • Ganglioneuroma / therapy*
  • Germany
  • Hospitals, Pediatric
  • Humans
  • Neuroblastoma / diagnosis*
  • Neuroblastoma / mortality
  • Neuroblastoma / therapy*
  • Prognosis
  • Risk Adjustment
  • Survival Rate