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

Author:

Zijtregtop Eline A. M.1,Zeal Jamie23,Metzger Monika L.24,Kelly Kara M.5,Mauz-Koerholz Christine67,Voss Stephan D.8ORCID,McCarten Kathleen9ORCID,Flerlage Jamie E.24ORCID,Beishuizen Auke110ORCID

Affiliation:

1. 1Department of Pediatric Oncology/Hematology, Erasmus MC-Sophia Children’s Hospital, Rotterdam, The Netherlands

2. 2Department of Pediatrics, University of Tennessee Health Sciences Center, Memphis, TN

3. 3Department of Medicine, University of Tennessee Health Sciences Center, Memphis, TN

4. 4Department of Oncology, St. Jude Children’s Research Hospital, Memphis, TN

5. 5Department of Pediatrics, Roswell Park Comprehensive Cancer Center, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, NY

6. 6Department of Pädiatrische Hämatologie und Onkologie, Zentrum für Kinderheilkunde der Justus-Liebig-Universität Giessen, Giessen, Germany

7. 7Medical Faculty, Martin-Luther-University of Halle-Wittenberg, Halle, Germany

8. 8Department of Radiology, Boston Children’s Hospital Dana-Farber Cancer Institute, Boston, MA

9. 9Imaging and Radiation Oncology Core-Rhode Island, Lincoln, RI

10. 10Department of Hemato-Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands

Abstract

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.

Publisher

American Society of Hematology

Subject

Hematology

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