Differentiation between rebound thymic hyperplasia and thymic relapse after chemotherapy in pediatric Hodgkin lymphoma

Author:

Franke Friedrich Christian1,Damek Adrian2,Steglich Jonas2,Kurch Lars3ORCID,Hasenclever Dirk4,Georgi Thomas W3,Wohlgemuth Walther Alexander2,Mauz‐Körholz Christine5,Körholz Dieter5,Kluge Regine3,Landman‐Parker Judith6,Wallace William Hamish7,Fosså Alexander8,Vordermark Dirk9,Karlen Jonas10,Fernández‐Teijeiro Ana11,Cepelova Michaela12ORCID,Klekawka Tomasz13,Attarbaschi Andishe14ORCID,Ceppi Francesco15,Hraskova Andrea16,Uyttebroeck Anne17,Beishuizen Auke1819,Dieckmann Karin20,Leblanc Thierry21,Moellers Martin22,Buerke Boris23,Stoevesandt Dietrich2ORCID

Affiliation:

1. Department of Radiology Diakoniekrankenhaus Halle Halle (Saale) Germany

2. Department of Radiology University Hospital Halle (Saale) Halle (Saale) Germany

3. Department of Nuclear Medicine University of Leipzig Leipzig Germany

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

5. Department of Pediatric Hematology and Oncology Justus‐Liebig University Gießen Germany

6. Sorbonne Université/APHP hôpital Trousseau Paris France

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

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

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

10. Karolinska University Hospital Astrid Lindgrens Childrens Hospital Stockholm Sweden

11. Pediatric Onco‐Hematology Unit Hospital Universitario Virgen Macarena Sevilla Spain

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

13. Pediatric Oncology and Hematology Department University Children's Hospital of Krakow Krakow Poland

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

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

16. Department of Pediatric Hematology and Oncology National Institute of Paediatric Diseases Bratislava Slovakia

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

18. Erasmus MC Sophia Children's Hospital Rotterdam The Netherlands

19. Princess Màxima Center for Pediatric Oncology Utrecht The Netherlands

20. Department of Radiation Oncology University Hospital Vienna Vienna Austria

21. Service d'Hématologie Pédiatrique Hôpital Robert‐Debré Paris France

22. Department Department of Pediatric Radiology University Bielefeld, Campus Bielefeld‐Bethel Bielefeld Germany

23. Department of Clinical Radiology University Hospital of Münster Münster Germany

Abstract

AbstractBackgroundRebound thymic hyperplasia (RTH) is a common phenomenon caused by stress factors such as chemotherapy (CTX) or radiotherapy, with an incidence between 44% and 67.7% in pediatric lymphoma. Misinterpretation of RTH and thymic lymphoma relapse (LR) may lead to unnecessary diagnostic procedures including invasive biopsies or treatment intensification. The aim of this study was to identify parameters that differentiate between RTH and thymic LR in the anterior mediastinum.MethodsAfter completion of CTX, we analyzed computed tomographies (CTs) and magnetic resonance images (MRIs) of 291 patients with classical Hodgkin lymphoma (CHL) and adequate imaging available from the European Network for Pediatric Hodgkin lymphoma C1 trial. In all patients with biopsy‐proven LR, an additional fluorodeoxyglucose (FDG)‐positron emission tomography (PET)‐CT was assessed. Structure and morphologic configuration in addition to calcifications and presence of multiple masses in the thymic region and signs of extrathymic LR were evaluated.ResultsAfter CTX, a significant volume increase of new or growing masses in the thymic space occurred in 133 of 291 patients. Without biopsy, only 98 patients could be identified as RTH or LR. No single finding related to thymic regrowth allowed differentiation between RTH and LR. However, the vast majority of cases with thymic LR presented with additional increasing tumor masses (33/34). All RTH patients (64/64) presented with isolated thymic growth.ConclusionIsolated thymic LR is very uncommon. CHL relapse should be suspected when increasing tumor masses are present in distant sites outside of the thymic area. Conversely, if regrowth of lymphoma in other sites can be excluded, isolated thymic mass after CTX likely represents RTH.

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

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