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Significance of E-lesions in Hodgkin lymphoma and the creation of a new consensus definition: a report from SEARCH

  • Eline A.M. Zijtregtop
  • , Jamie Zeal
  • , Monika L. Metzger
  • , Kara M. Kelly
  • , Christine Mauz-Koerholz
  • , Stephan D. Voss
  • , Kathleen McCarten
  • , Jamie E. Flerlage
  • , Auke Beishuizen
  • Erasmus University Rotterdam
  • University of Tennessee Health Science Center
  • St. Jude Children Research Hospital
  • Justus Liebig University Giessen
  • Martin Luther University Halle-Wittenberg
  • Dana-Farber Cancer Institute
  • Imaging and Radiation Oncology Core Rhode Island
  • Princess Máxima Center for Pediatric Oncology

Research output: Contribution to journalReview articlepeer-review

10 Scopus citations

Abstract

The International Staging Evaluation and Response Criteria Harmonization for Childhood, Adolescent, and Young Adult Hodgkin Lymphoma (SEARCH for CAYAHL) seeks to provide an appropriate, universal differentiation between E-lesions and stage IV extranodal disease in Hodgkin lymphoma (HL). A literature search was performed through the PubMed and Google Scholar databases using the terms “Hodgkin disease,” and “extranodal,” “extralymphatic,” “E lesions,” “E stage,” or “E disease.” Publications were reviewed for the number of participants; median age and age range; diagnostic modalities used for staging; and the definition, incidence, and prognostic significance of E-lesions. Thirty-six articles describing 12 640 patients met the inclusion criteria. Most articles reported staging per the Ann Arbor (72%, 26/36) or Cotswolds modification of the Ann Arbor staging criteria (25%, 9/36), and articles rarely defined E-lesions or disambiguated “extranodal disease.” The overall incidence of E-lesions for patients with stage I-III HL was 11.5% (1330/11 602 unique patients). Available stage-specific incidence analysis of 3888 patients showed a similar incidence of E-lesions in stage II (21.2%) and stage III (21.9%), with E-lesions rarely seen with stage I disease (1.1%). E-lesions likely remain predictive, but we cannot unequivocally conclude that identifying E-lesions in HL imparts prognostic value in the modern era of the more selective use of targeted radiation therapy. A harmonized E-lesion definition was reached based on the available evidence and the consensus of the SEARCH working group. We recommend that this definition of E-lesion be applied in future clinical trials with explicit reporting to confirm the prognostic value of E-lesions.

Original languageEnglish
Pages (from-to)6303-6319
Number of pages17
JournalBlood Advances
Volume7
Issue number20
DOIs
StatePublished - Oct 24 2023

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