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Dodecafluoropentane Emulsion as a Radiosensitizer in Glioblastoma Multiforme.

Authors :
Lickliter JD
Ruben J
Kichenadasse G
Jennens R
Gzell C
Mason RP
Zhou H
Becker J
Unger E
Stea B
Source :
Cancer research communications [Cancer Res Commun] 2023 Aug 21; Vol. 3 (8), pp. 1607-1614. Date of Electronic Publication: 2023 Aug 21 (Print Publication: 2023).
Publication Year :
2023

Abstract

Purpose: Glioblastoma multiforme (GBM) is a hypoxic tumor resistant to radiotherapy. The purpose of this study was to assess the safety and efficacy of a novel oxygen therapeutic, dodecafluoropentane emulsion (DDFPe), in chemoradiation treatment of GBM.<br />Experimental Design: In this multicenter phase Ib/II dose-escalation study, patients were administered DDFPe via intravenous infusion (0.05, 0.10, or 0.17 mL/kg) while breathing supplemental oxygen prior to each 2 Gy fraction of radiotherapy (30 fractions over 6 weeks). Patients also received standard-of-care chemotherapy [temozolomide (TMZ)]. Serial MRI scans were taken to monitor disease response. Adverse events were recorded and graded. TOLD (tissue oxygenation level-dependent) contrast MRI was obtained to validate modulation of tumor hypoxia.<br />Results: Eleven patients were enrolled. DDFPe combined with radiotherapy and TMZ was well tolerated in most patients. Two patients developed delayed grade 3 radiation necrosis during dose escalation, one each at 0.1 and 0.17 mL/kg of DDFPe. Subsequent patients were treated at the 0.1 mL/kg dose level. Kaplan-Meier analysis showed a median overall survival of 19.4 months and a median progression-free survival of 9.6 months, which compares favorably to historical controls. Among 6 patients evaluable for TOLD MRI, a statistically significant reduction in tumor T <subscript>1</subscript> was observed after DDFPe treatment.<br />Conclusions: This trial, although small, showed that the use of DDFPe as a radiosensitizer in patients with GBM was generally safe and may provide a survival benefit. This is also the first time than TOLD MRI has shown reversal of tumor hypoxia in a clinical trial in patients. The recommended dose for phase II evaluation is 0.1 mL/kg DDFPe.Trial Registration: NCT02189109.<br />Significance: This study shows that DDFPe can be safely administered to patients, and it is the first-in-human study to show reversal of hypoxia in GBM as measured by TOLD MRI. This strategy is being used in a larger phase II/III trial which will hopefully show a survival benefit by adding DDFPe during the course of fractionated radiation and concurrent chemotherapy.<br /> (© 2023 The Authors; Published by the American Association for Cancer Research.)

Details

Language :
English
ISSN :
2767-9764
Volume :
3
Issue :
8
Database :
MEDLINE
Journal :
Cancer research communications
Publication Type :
Academic Journal
Accession number :
37609003
Full Text :
https://doi.org/10.1158/2767-9764.CRC-22-0433