Haematotoxicity of craniospinal radiochemotherapy for metastatic paediatric high-grade glioma
Aims - Paediatric high-grade gliomas (pedHGGs) have a dismal prognosis, often characterised by early and diffuse disease progression. Novel treatment approaches are urgently needed to improve outcomes. The upcoming SIOPE-HGG (High Grade Glioma)-01 trial will investigate upfront craniospinal radioche...
Saved in:
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
December 2025
|
| In: |
Clinical oncology
Year: 2025, Volume: 48, Pages: 1-8 |
| ISSN: | 1433-2981 |
| DOI: | 10.1016/j.clon.2025.103956 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.clon.2025.103956 Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0936655525002110 |
| Author Notes: | C. Valentini, T. Perwein, B. Bison, G.H. Gielen, F. Knerlich-Lukoschus, H.C. Bock, C. Seidel, R.D. Kortmann, D. Sturm, M. Benesch, G. Nussbaumer, J.M. Krischer, A.O. von Bueren, M. Eyrich, L.L. Friker, M. Hoffmann, E. Gkika, A. Wittig-Sauerwein, J. Hörner-Rieber, R. Schwarz, K. Jablonska, W. Hoffmann, D. Vordermark, S. Rieken, L. Höng, C. Rödel, B. Timmermann, J.T. Fennell, A. Claviez, M. Karremann, C.M. Kramm, M. Krause |
| Summary: | Aims - Paediatric high-grade gliomas (pedHGGs) have a dismal prognosis, often characterised by early and diffuse disease progression. Novel treatment approaches are urgently needed to improve outcomes. The upcoming SIOPE-HGG (High Grade Glioma)-01 trial will investigate upfront craniospinal radiochemotherapy (CSI-RCT) for newly diagnosed, nonmetastatic diffuse midline glioma/diffuse intrinsic pontine glioma (DMG/DIPG). As CSI-RCT is frequently avoided due to concerns over haematotoxicity, real-world feasibility data are critically needed. - Materials and methods - We retrospectively assessed haematological toxicity in 19 patients (aged 3-21 years) with metastatic pedHGG treated with CSI-RCT within the hirn tumor glioblastoma trial (HIT-HGG) and hospital in trial-glioblastoma (HIT-GBM) trial programmes (2002-2024). All patients received craniospinal irradiation (median dose: 35.2 Gy) using photon- or proton-based techniques, with concurrent chemotherapy: temozolomide (TMZ; n = 14) or PEI (cisplatin, etoposide, ifosfamide; n = 5). Haematological toxicities were graded according to Common Terminology Criteria for Adverse Events (CTCAE) v4.0. - Results - Grade 3 to 4 haematotoxicity was observed in 7 of 19 patients (36.8%). Chemotherapy was discontinued in two cases—one due to TMZ-induced aplastic anaemia (TIAA) and another due to thrombocytopaenia. The remaining patients tolerated full-dose CSI-RCT with manageable side effects, and no unplanned radiotherapy interruptions occurred. The haematotoxicity rate was comparable to or lower than previous reports, indicating that CSI-RCT is feasible with appropriate monitoring and management. - Conclusion - This is the largest cohort to date assessing haematological toxicity of upfront CSI-RCT in metastatic pedHGG. Despite notable haematotoxicity, treatment was largely feasible and well-tolerated. These findings support the integration of CSI-RCT into future clinical trials for newly diagnosed DMG/DIPG and provide a foundation for the upcoming SIOPE HGG-01 trial. Proton therapy may further reduce toxicity and warrants prospective evaluation. |
|---|---|
| Item Description: | Gesehen am 20.01.2026 |
| Physical Description: | Online Resource |
| ISSN: | 1433-2981 |
| DOI: | 10.1016/j.clon.2025.103956 |