Iron-based biomarkers for personalizing pharmacological ascorbate therapy in glioblastoma: insights from a phase 2 clinical trial.

V A Magnotta, B J Smith, C Y Lee, M S Petronek, K L Bodeker, J M Buatti, B G Allen, N Teferi, K L Eschbacher, K A Jones, B T Loeffler

Journal: Journal of neuro-oncology 2024;166(3):493-501

PMID: 38285244

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.

© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

Address: Department of Radiation Oncology, Division of Free Radical and Radiation Biology, University of Iowa, Iowa City, IA, USA. [email protected].; Department of Radiation Oncology, Division of Free Radical and Radiation Biology, University of Iowa, Iowa City, IA, USA.; Department of Radiology, University of Iowa, Iowa City, IA, USA.; Department of Pathology, University of Iowa, Iowa City, IA, USA.; Department of Pathology, Division of Neuropathology, Duke University, Durham, NC, USA.; Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, USA.; Department of Biostatistics, University of Iowa, Iowa City, IA, USA.

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