Abstract

ObjectiveRadiotherapy (RT) is an integral part of the interdisciplinary treatment of patients with high-risk neuroblastoma (NB). With the continuous improvements of outcome, the interest in local treatment strategies that reduce treatment-related side effects while achieving optimal oncological results is growing. Proton beam therapy (PBT) represents a promising alternative to conventional photon irradiation with regard to the reduction of treatment burden.MethodRetrospective analysis of children with high or intermediate risk NB receiving PBT of the primary tumor site during first-line therapy between 2015 and 2020 was performed. Data from the prospective in-house registry Standard Protonentherapie WPE – Kinder- (KiProReg) with respect to tumor control and treatment toxicity were analyzed. Adverse events were classified according to CTCAE Version 4 (V4.0) before, during, and after PBT.ResultsIn total, 44 patients (24 male, 20 female) with high (n = 39) or intermediate risk NB (n = 5) were included in the analysis. Median age was 3.4 years (range, 1.4–9.9 years). PBT doses ranged from 21.0 to 39.6 Gray (Gy) (median 36.0 Gy). Five patients received PBT to the MIBG-avid residual at the primary tumor site at time of PBT according to the NB-2004 protocol. In 39 patients radiation was given to the pre-operative tumor bed with or without an additional boost in case of residual tumor. After a median follow-up (FU) of 27.6 months, eight patients developed progression, either local recurrence (n = 1) or distant metastases (n = 7). Four patients died due to tumor progression. At three years, the estimated local control, distant metastatic free survival, progression free survival, and overall survival was 97.7, 84.1, 81.8, and 90.9%, respectively. During radiation, seven patients experienced higher-grade (CTCAE ≥ °3) hematologic toxicity. No other higher grade acute toxicity occurred. After PBT, one patient developed transient myelitis while receiving immunotherapy. No higher grade long-term toxicity was observed up to date.ConclusionPBT was a well tolerated and effective local treatment in children with high and intermediate risk NB. The role of RT in an intensive multidisciplinary treatment regimen remains to be studied in the future in order to better define timing, doses, target volumes, and general need for RT in a particularly sensitive cohort of patients.

Highlights

  • Neuroblastoma (NB) is the most common extracranial solid tumor of childhood

  • Our original data displays excellent safety, feasibility and high tumor control gathered from a prospective monoinstitutional registry

  • Local control and survival rates were similar to other studies, which demonstrated a 3- to 5-year local control (LC)

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Summary

Introduction

Neuroblastoma (NB) is the most common extracranial solid tumor of childhood. It has been identified as a neuroectodermal embryonal malignant tumor affecting the sympathetic nervous tissue. The age of >18 months at diagnosis, the detection of amplification of the oncogene MYCN and the presence of distant metastases are well known risk factors for worse disease control and survival [2]. The 5year survival rate of patients with high-risk NB is below 50% [7]. Considering the very young age of the affected children, the position of the tumor close to the radiation sensitive organs, such as kidneys and spinal medulla, and the intensive multi-agent chemotherapy applied prior to radiation, proton beam therapy (PBT) represents a promising alternative to conventional photon irradiation. The current study reports on our experiences when treating patients with NB with special consideration of PBT in an intensive multimodal therapy concept

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