Evaluation of dose, volume, and outcome in children with localized, intracranial ependymoma treated with proton therapy within the prospective KiProReg Study

Author:

Peters Sarah12ORCID,Merta Julien12,Schmidt Laura2,Jazmati Danny12,Kramer Paul-Heinz2,Blase Cristoph3,Tippelt Stephan4,Fleischhack Gudrun4,Stock Annika5,Bison Brigitte6,Rutkowski Stefan7,Pietsch Torsten8ORCID,Kortmann Rolf-Dieter9ORCID,Timmermann Beate1011

Affiliation:

1. West German Proton Therapy Center Essen (WPE), University Hospital Essen, Essen, Germany

2. Clinic for Particle Therapy, University Hospital Essen, Essen, Germany

3. AnästhesieNetz Rhein-Ruhr, Bochum, Germany

4. Department of Pediatrics III, University Hospital Essen, Essen, Germany

5. Department of Neuroradiology, University Hospital Wuerzburg, Wuerzburg, Germany

6. Department of Diagnostic and Interventional Neuroradiology, University Hospital Augsburg, Augsburg, Germany

7. Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

8. Institute of Neuropathology, DGNN Brain Tumor Reference Center, University of Bonn Medical Center, Bonn, Germany

9. Department of Radiotherapy and Radio-oncology, University Hospital Leipzig, Leipzig, Germany

10. West German Cancer Center (WTZ), University Hospital Essen, Essen, Germany

11. German Cancer Consortium (DKTK), Essen, Germany

Abstract

Abstract Background Radiotherapy (RT) of ependymoma in children is an important part of the interdisciplinary treatment concept. However, feasibility and dose concepts are still under investigation, particularly in very young children. The aim of this study was to evaluate the standard dose and volume of proton therapy (PT) in children with ependymoma. Methods In this analysis, 105 patients with localized, intracranial ependymoma under the age of 18 years treated with PT between 2013 and 2018 were included. Patient characteristics, treatment, outcome, and follow-up data were analyzed using descriptive statistics, Kaplan-Meier, and Cox regression analysis. Results The median age of patients at PT was 2.8 years (0.9-17.0 years). The molecular subgroup analysis was performed in a subset of 50 patients (37 EP-PFA, 2 EP-PFB, 7 EP-RELA, 2 EP-YAP, 2 NEC [not elsewhere classified]). The median total dose was 59.4 Gy (54.0-62.0 Gy). The median follow-up time was 1.9 years. The estimated 3-year overall survival (OS), local control (LC), and progression-free survival (PFS) rates were 93.7%, 74.1%, and 55.6%, respectively. Within univariable analysis, female gender and lower dose had a positive impact on OS, whereas age ≥4 years had a negative impact on OS and PT given after progression had a negative impact on PFS. In the multivariable analysis, multiple tumor surgeries were associated with lower PFS. New ≥3° late toxicities occurred in 11 patients. Conclusion For children with localized ependymoma, PT was effective and well tolerable. Multiple surgeries showed a negative impact on PFS.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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