Assessment of Waldeyer's ring in pediatric and adolescent Hodgkin lymphoma patients-Importance of multimodality imaging: Results from the EuroNet-PHL-C1 trial.


Journal

Pediatric blood & cancer
ISSN: 1545-5017
Titre abrégé: Pediatr Blood Cancer
Pays: United States
ID NLM: 101186624

Informations de publication

Date de publication:
04 2021
Historique:
received: 24 11 2020
revised: 29 12 2020
accepted: 30 12 2020
pubmed: 5 2 2021
medline: 10 8 2021
entrez: 4 2 2021
Statut: ppublish

Résumé

In the EuroNet Pediatric Hodgkin Lymphoma (EuroNet-PHL) trials, decision on Waldeyer's ring (WR) involvement is usually based on clinical assessment, that is, physical examination and/or nasopharyngoscopy. However, clinical assessment only evaluates mucosal surface and is prone to interobserver variability. Modern cross-sectional imaging technology may provide valuable information beyond mucosal surface, which may lead to a more accurate WR staging. The EuroNet-PHL-C1 trial recruited 2102 patients, of which 1752 underwent central review including reference reading of their cross-sectional imaging data. In 14 of 1752 patients, WR was considered involved according to clinical assessment. In these 14 patients, the WR was re-assessed by applying an imaging-based algorithm considering information from The imaging-based algorithm confirmed WR involvement only in four of the 14 patients. Of the remaining 10 patients, four had retropharyngeal lymph node involvement and six an inconspicuous WR. Applying the imaging-based algorithm to 100 consecutive patients with physiological appearance of their WR on clinical assessment, absence of WR involvement could be confirmed in 99. However, suspicion of WR involvement was raised in one patient. The imaging-based algorithm was feasible and easily applicable at initial staging of young patients with Hodgkin lymphoma. It increased the accuracy of WR staging, which may contribute to a more individualized treatment in the future.

Sections du résumé

BACKGROUND
In the EuroNet Pediatric Hodgkin Lymphoma (EuroNet-PHL) trials, decision on Waldeyer's ring (WR) involvement is usually based on clinical assessment, that is, physical examination and/or nasopharyngoscopy. However, clinical assessment only evaluates mucosal surface and is prone to interobserver variability. Modern cross-sectional imaging technology may provide valuable information beyond mucosal surface, which may lead to a more accurate WR staging.
PATIENTS, MATERIALS, AND METHODS
The EuroNet-PHL-C1 trial recruited 2102 patients, of which 1752 underwent central review including reference reading of their cross-sectional imaging data. In 14 of 1752 patients, WR was considered involved according to clinical assessment. In these 14 patients, the WR was re-assessed by applying an imaging-based algorithm considering information from
RESULTS
The imaging-based algorithm confirmed WR involvement only in four of the 14 patients. Of the remaining 10 patients, four had retropharyngeal lymph node involvement and six an inconspicuous WR. Applying the imaging-based algorithm to 100 consecutive patients with physiological appearance of their WR on clinical assessment, absence of WR involvement could be confirmed in 99. However, suspicion of WR involvement was raised in one patient.
CONCLUSIONS
The imaging-based algorithm was feasible and easily applicable at initial staging of young patients with Hodgkin lymphoma. It increased the accuracy of WR staging, which may contribute to a more individualized treatment in the future.

Identifiants

pubmed: 33538093
doi: 10.1002/pbc.28903
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e28903

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 The Authors. Pediatric Blood & Cancer published by Wiley Periodicals LLC.

Références

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Auteurs

Lars Kurch (L)

Department of Nuclear Medicine, University of Leipzig, Leipzig, Germany.

Christine Mauz-Körholz (C)

Department of Pediatric Hematology and Oncology, Justus-Liebig University, Gießen, Germany.
Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Alexander Fosså (A)

Department of Medical Oncology and Radiotherapy, Oslo University Hospital, Oslo, Norway.

Thomas Walther Georgi (TW)

Department of Nuclear Medicine, University of Leipzig, Leipzig, Germany.

Regine Kluge (R)

Department of Nuclear Medicine, University of Leipzig, Leipzig, Germany.

Jörg Martin Bartelt (JM)

Department of Radiology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Christian Kunze (C)

Department of Radiology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Walter Alexander Wohlgemuth (WA)

Department of Radiology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Tanja Pelz (T)

Department of Radiation Oncology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Dirk Vordermark (D)

Department of Radiation Oncology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

Sebastian Plößl (S)

Department of Ear, Nose and Throat Medicine, Hospital Martha-Maria Halle, Halle (Saale), Germany.

Dirk Hasenclever (D)

Institute for Medical Informatics, Statistics and Epidemiology (IMISE), University of Leipzig, Leipzig, Germany.

Osama Sabri (O)

Department of Nuclear Medicine, University of Leipzig, Leipzig, Germany.

Judith Landman-Parker (J)

Hôpital Armand-Trousseau Sorbonne Universitè, Paris, France.

William Hamish Wallace (WH)

Department of Paediatric Oncology, Royal Hospital for Sick Children, University of Edinburgh, Edinburgh, UK.

Jonas Karlen (J)

Karolinska University Hospital, Astrid Lindgrens Childrens Hospital, Stockholm, Sweden.

Ana Fernández-Teijeiro (A)

Pediatric Onco-Hematology Unit, Hospital Universitario Virgen Macarena, Sevilla, Spain.

Michaela Cepelova (M)

Department of Pediatric Hematology and Oncology, University Hospital Motol and, Second Medical Faculty of Charles University, Prague, Czech Republic.

Tomasz Klekawka (T)

Institute of Pediatrics, Jagiellonian University Medical College, Krakow, Poland.

Ayca Muftuler Løndalen (AM)

Department of Radiology and Nuclear Medicine, Oslo University Hospital, Oslo, Norway.

Dagmar Steiner (D)

Department of Nuclear Medicine, Justus-Liebig University Giessen, Giessen, Germany.

Gabriele Krombach (G)

Department of Radiology, Justus-Liebig University Giessen, Giessen, Germany.

Andishe Attarbaschi (A)

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.

Martha Hoffmann (M)

Wiener Privatklinik, Radiology Centre, Vienna, Austria.

Francesco Ceppi (F)

Division of Pediatrics, Department of Woman-, Mother-Child, Pediatric Hematology-Oncology Unit, University Hospital of Lausanne, Lausanne, Switzerland.

Jane Pears (J)

Department of Pediatric Hematology and Oncology, Our Lady's Children's Hospital, Dublin, Ireland.

Andrea Hraskova (A)

Department of Pediatric Hematology and Oncology, University Children's Hospital, Bratislava, Slovakia.

Anne Uyttebroeck (A)

Department of Pediatric Hematology and Oncology, University Hospitals Leuven, Leuven, Belgium.

Auke Beishuizen (A)

Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
Princess Màxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Karin Dieckmann (K)

Department of Radiation Oncology, University Hospital Vienna, Vienna, Austria.

Thierry Leblanc (T)

Service d'Hématologie Pédiatrique, Hôpital Robert-Debré, Paris, France.

Stephen Daw (S)

Department of Pediatric Hematology and Oncology, University College London Hospitals, London, UK.

Dieter Körholz (D)

Department of Pediatric Hematology and Oncology, Justus-Liebig University, Gießen, Germany.

Dietrich Stoevesandt (D)

Department of Radiology, Medical Faculty of the Martin-Luther-University, Halle (Saale), Germany.

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