Phase I trial of intranasal NEO100, highly purified perillyl alcohol, in adult patients with recurrent glioblastoma.

O6-methylguanine-DNA methyltransferase intranasal isocitrate dehydrogenase 1 perillyl alcohol recurrent glioblastoma

Journal

Neuro-oncology advances
ISSN: 2632-2498
Titre abrégé: Neurooncol Adv
Pays: England
ID NLM: 101755003

Informations de publication

Date de publication:
Historique:
entrez: 19 2 2021
pubmed: 20 2 2021
medline: 20 2 2021
Statut: epublish

Résumé

Better treatments for glioblastoma (GBM) patients, in particular in the recurrent setting, are urgently needed. Clinical trials performed in Brazil indicated that intranasal delivery of perillyl alcohol (POH) might be effective in this patient group. NEO100, a highly purified version of POH, was current good manufacturing practice (cGMP) manufactured to evaluate the safety and efficacy of this novel approach in a Phase I/IIa clinical trial in the United States. A total of 12 patients with recurrent GBM were enrolled into Phase I of this trial. NEO100 was administered by intranasal delivery using a nebulizer and nasal mask. Dosing was 4 times a day, every day. Four cohorts of 3 patients received the following dosages: 96 mg/dose (384 mg/day), 144 mg/dose (576 mg/day), 192 mg/dose (768 mg/day), and 288 mg/dose (1152 mg/day). Completion of 28 days of treatment was recorded as 1 cycle. Adverse events were documented, and radiographic response Intranasal NEO100 was well tolerated at all dose levels and no severe adverse events were reported. PFS-6 was 33%, OS-12 was 55%, and median OS was 15 months. Four patients (33%), all of them with isocitrate dehydrogenase 1 (IDH1)-mutant tumors, survived >24 months. Intranasal glioma therapy with NEO100 was well tolerated. It correlated with improved survival when compared to historical controls, pointing to the possibility that this novel intranasal approach could become useful for the treatment of recurrent GBM.

Sections du résumé

BACKGROUND BACKGROUND
Better treatments for glioblastoma (GBM) patients, in particular in the recurrent setting, are urgently needed. Clinical trials performed in Brazil indicated that intranasal delivery of perillyl alcohol (POH) might be effective in this patient group. NEO100, a highly purified version of POH, was current good manufacturing practice (cGMP) manufactured to evaluate the safety and efficacy of this novel approach in a Phase I/IIa clinical trial in the United States.
METHODS METHODS
A total of 12 patients with recurrent GBM were enrolled into Phase I of this trial. NEO100 was administered by intranasal delivery using a nebulizer and nasal mask. Dosing was 4 times a day, every day. Four cohorts of 3 patients received the following dosages: 96 mg/dose (384 mg/day), 144 mg/dose (576 mg/day), 192 mg/dose (768 mg/day), and 288 mg/dose (1152 mg/day). Completion of 28 days of treatment was recorded as 1 cycle. Adverse events were documented, and radiographic response
RESULTS RESULTS
Intranasal NEO100 was well tolerated at all dose levels and no severe adverse events were reported. PFS-6 was 33%, OS-12 was 55%, and median OS was 15 months. Four patients (33%), all of them with isocitrate dehydrogenase 1 (IDH1)-mutant tumors, survived >24 months.
CONCLUSION CONCLUSIONS
Intranasal glioma therapy with NEO100 was well tolerated. It correlated with improved survival when compared to historical controls, pointing to the possibility that this novel intranasal approach could become useful for the treatment of recurrent GBM.

Identifiants

pubmed: 33604574
doi: 10.1093/noajnl/vdab005
pii: vdab005
pmc: PMC7879254
doi:

Types de publication

Journal Article

Langues

eng

Pagination

vdab005

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

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Auteurs

Axel H Schönthal (AH)

Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

David M Peereboom (DM)

Department of Medical Oncology, Cleveland Clinic, Cleveland, Ohio, USA.

Naveed Wagle (N)

Department of Oncology, Providence St. Johns Medical Center, Santa Monica, California, USA.

Rose Lai (R)

Department of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Anna J Mathew (AJ)

Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Kyle M Hurth (KM)

Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Vincent F Simmon (VF)

NeOnc Technologies, Inc., Los Angeles, California, USA.

Steven P Howard (SP)

Department of Radiation Oncology, University of Wisconsin, Madison, Wisconsin, USA.

Lynne P Taylor (LP)

Department of Medicine, University of Washington, Seattle, Washington, USA.

Frances Chow (F)

Department of Neurology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Clovis O da Fonseca (CO)

NeOnc Technologies, Inc., Los Angeles, California, USA.
Department of General and Specialized Surgery, Antonio Pedro University Hospital, Fluminense Federal University, Niterói, Rio de Janeiro, Brazil.

Thomas C Chen (TC)

Department of Pathology, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
NeOnc Technologies, Inc., Los Angeles, California, USA.
Department of Neurological Surgery, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

Classifications MeSH