Positron emission tomography has a high negative predictive value for progression or early relapse for patients with residual disease after first-line chemotherapy in advanced-stage Hodgkin lymphoma.

  • Carsten Kobe
  • Markus Dietlein
  • Jeremy Franklin
  • Jana Markova
  • Andreas Lohri
  • Holger Amthauer
  • Susanne Klutmann
  • Wolfram H Knapp
  • Josee M Zijlstra
  • Andreas Bockisch
  • Matthias Weckesser
  • Reinhard Lorenz
  • Mathias Schreckenberger
  • Roland Bares
  • Hans T Eich
  • Rolf-Peter Mueller
  • Michael Fuchs
  • Peter Borchmann
  • Harald Schicha
  • Volker Diehl
  • Andreas Engert

Abstract

In the HD15 trial of the German Hodgkin Study Group, the negative predictive value (NPV) of positron emission tomography (PET) using [(18)F]-fluorodeoxyglucose in advanced-stage Hodgkin lymphoma (HL) was evaluated. A total of 817 patients were enrolled and randomly assigned to receive BEACOPP-based chemotherapy. After completion of chemotherapy, residual disease measuring more than or equal to 2.5 cm in diameter was assessed by PET in 311 patients. The NPV of PET was defined as the proportion of PET(-) patients without progression, relapse, or irradiation within 12 months after PET review panel. The progression-free survival was 96% for PET(-) patients (95% confidence interval [CI], 94%-99%) and 86% for PET(+) patients (95% CI, 78%-95%, P = .011). The NPV for PET in this analysis was 94% (95% CI, 91%-97%). Thus, consolidation radiotherapy can be omitted in PET(-) patients with residual disease without increasing the risk for progression or early relapse compared with patients in complete remission. The impact of this finding on the overall survival at 5 years must be awaited. Until then, response adapted therapy guided by PET for HL patients seems to be a promising approach that should be further evaluated in clinical trials. This trial is registered at http://isrctn.org study as #ISRCTN32443041.

Bibliographical data

Original languageGerman
Article number10
ISSN0006-4971
Publication statusPublished - 2008
pubmed 18757777