Erschienen in:
29.01.2024 | Research
Iron-based biomarkers for personalizing pharmacological ascorbate therapy in glioblastoma: insights from a phase 2 clinical trial
verfasst von:
M. S. Petronek, K. L. Bodeker, C. Y. Lee, N. Teferi, K. L. Eschbacher, K. A. Jones, B. T. Loeffler, B. J. Smith, J. M. Buatti, V. A. Magnotta, B. G. Allen
Erschienen in:
Journal of Neuro-Oncology
|
Ausgabe 3/2024
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Abstract
Background
Pharmacological ascorbate (intravenous delivery reaching plasma concentrations ≈ 20 mM; P-AscH−) has emerged as a promising therapeutic strategy for glioblastoma. Recently, a single-arm phase 2 clinical trial demonstrated a significant increase in overall survival when P-AscH− was combined with temozolomide and radiotherapy. As P-AscH− relies on iron-dependent mechanisms, this study aimed to assess the predictive potential of both molecular and imaging-based iron-related markers to enhance the personalization of P-AscH− therapy in glioblastoma participants.
Methods
Participants (n = 55) with newly diagnosed glioblastoma were enrolled in a phase 2 clinical trial conducted at the University of Iowa (NCT02344355). Tumor samples obtained during surgical resection were processed and stained for transferrin receptor and ferritin heavy chain expression. A blinded pathologist performed pathological assessment. Quantitative susceptibility mapping (QSM) measures were obtained from pre-radiotherapy MRI scans following maximal safe surgical resection. Circulating blood iron panels were evaluated prior to therapy through the University of Iowa Diagnostic Laboratory.
Results
Through univariate analysis, a significant inverse association was observed between tumor transferrin receptor expression and overall and progression-free survival. QSM measures exhibited a significant, positive association with progression-free survival. Subjects were actively followed until disease progression and then were followed through chart review or clinical visits for overall survival.
Conclusions
This study analyzes iron-related biomarkers in the context of P-AscH− therapy for glioblastoma. Integrating molecular, systemic, and imaging-based markers offers a multifaceted approach to tailoring treatment strategies, thereby contributing to improved patient outcomes and advancing the field of glioblastoma therapy.