TY - JOUR
T1 - Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma
AU - Gállego Pérez-Larraya, Jaime
AU - Garcia-Moure, Marc
AU - Labiano, Sara
AU - Patiño-García, Ana
AU - Dobbs, Jessica
AU - Gonzalez-Huarriz, Marisol
AU - Zalacain, Marta
AU - Marrodan, Lucia
AU - Martinez-Velez, Naiara
AU - Puigdelloses, Montserrat
AU - Laspidea, Virginia
AU - Astigarraga, Itziar
AU - Lopez-Ibor, Blanca
AU - Cruz, Ofelia
AU - Oscoz Lizarbe, Miren
AU - Hervas-Stubbs, Sandra
AU - Alkorta-Aranburu, Gorka
AU - Tamayo, Ibon
AU - Tavira, Beatriz
AU - Hernandez-Alcoceba, Ruben
AU - Jones, Chris
AU - Dharmadhikari, Gitanjali
AU - Ruiz-Moreno, Cristian
AU - Stunnenberg, Henk
AU - Hulleman, Esther
AU - van der Lugt, Jasper
AU - Idoate, Miguel Á
AU - Diez-Valle, Ricardo
AU - Esparragosa Vázquez, Inés
AU - Villalba, Maria
AU - de Andrea, Carlos
AU - Núñez-Córdoba, Jorge M
AU - Ewald, Brett
AU - Robbins, Joan
AU - Fueyo, Juan
AU - Gomez-Manzano, Candelaria
AU - Lang, Frederick F
AU - Tejada, Sonia
AU - Alonso, Marta M
N1 - Publisher Copyright:
© 2022 Massachusetts Medical Society.
PY - 2022/6/30
Y1 - 2022/6/30
N2 - BACKGROUND: Pediatric patients with diffuse intrinsic pontine glioma (DIPG) have a poor prognosis, with a median survival of less than 1 year. Oncolytic viral therapy has been evaluated in patients with pediatric gliomas elsewhere in the brain, but data regarding oncolytic viral therapy in patients with DIPG are lacking.METHODS: We conducted a single-center, dose-escalation study of DNX-2401, an oncolytic adenovirus that selectively replicates in tumor cells, in patients with newly diagnosed DIPG. The patients received a single virus infusion through a catheter placed in the cerebellar peduncle, followed by radiotherapy. The primary objective was to assess the safety and adverse-event profile of DNX-2401. The secondary objectives were to evaluate the effect of DNX-2401 on overall survival and quality of life, to determine the percentage of patients who have an objective response, and to collect tumor-biopsy and peripheral-blood samples for correlative studies of the molecular features of DIPG and antitumor immune responses.RESULTS: A total of 12 patients, 3 to 18 years of age, with newly diagnosed DIPG received 1×1010 (the first 4 patients) or 5×1010 (the subsequent 8 patients) viral particles of DNX-2401, and 11 received subsequent radiotherapy. Adverse events among the patients included headache, nausea, vomiting, and fatigue. Hemiparesis and tetraparesis developed in 1 patient each. Over a median follow-up of 17.8 months (range, 5.9 to 33.5), a reduction in tumor size, as assessed on magnetic resonance imaging, was reported in 9 patients, a partial response in 3 patients, and stable disease in 8 patients. The median survival was 17.8 months. Two patients were alive at the time of preparation of the current report, 1 of whom was free of tumor progression at 38 months. Examination of a tumor sample obtained during autopsy from 1 patient and peripheral-blood studies revealed alteration of the tumor microenvironment and T-cell repertoire.CONCLUSIONS: Intratumoral infusion of oncolytic virus DNX-2401 followed by radiotherapy in pediatric patients with DIPG resulted in changes in T-cell activity and a reduction in or stabilization of tumor size in some patients but was associated with adverse events. (Funded by the European Research Council under the European Union's Horizon 2020 Research and Innovation Program and others; EudraCT number, 2016-001577-33; ClinicalTrials.gov number, NCT03178032.).
AB - BACKGROUND: Pediatric patients with diffuse intrinsic pontine glioma (DIPG) have a poor prognosis, with a median survival of less than 1 year. Oncolytic viral therapy has been evaluated in patients with pediatric gliomas elsewhere in the brain, but data regarding oncolytic viral therapy in patients with DIPG are lacking.METHODS: We conducted a single-center, dose-escalation study of DNX-2401, an oncolytic adenovirus that selectively replicates in tumor cells, in patients with newly diagnosed DIPG. The patients received a single virus infusion through a catheter placed in the cerebellar peduncle, followed by radiotherapy. The primary objective was to assess the safety and adverse-event profile of DNX-2401. The secondary objectives were to evaluate the effect of DNX-2401 on overall survival and quality of life, to determine the percentage of patients who have an objective response, and to collect tumor-biopsy and peripheral-blood samples for correlative studies of the molecular features of DIPG and antitumor immune responses.RESULTS: A total of 12 patients, 3 to 18 years of age, with newly diagnosed DIPG received 1×1010 (the first 4 patients) or 5×1010 (the subsequent 8 patients) viral particles of DNX-2401, and 11 received subsequent radiotherapy. Adverse events among the patients included headache, nausea, vomiting, and fatigue. Hemiparesis and tetraparesis developed in 1 patient each. Over a median follow-up of 17.8 months (range, 5.9 to 33.5), a reduction in tumor size, as assessed on magnetic resonance imaging, was reported in 9 patients, a partial response in 3 patients, and stable disease in 8 patients. The median survival was 17.8 months. Two patients were alive at the time of preparation of the current report, 1 of whom was free of tumor progression at 38 months. Examination of a tumor sample obtained during autopsy from 1 patient and peripheral-blood studies revealed alteration of the tumor microenvironment and T-cell repertoire.CONCLUSIONS: Intratumoral infusion of oncolytic virus DNX-2401 followed by radiotherapy in pediatric patients with DIPG resulted in changes in T-cell activity and a reduction in or stabilization of tumor size in some patients but was associated with adverse events. (Funded by the European Research Council under the European Union's Horizon 2020 Research and Innovation Program and others; EudraCT number, 2016-001577-33; ClinicalTrials.gov number, NCT03178032.).
KW - Adenoviridae
KW - Adolescent
KW - Astrocytoma/radiotherapy
KW - Brain Stem Neoplasms/mortality
KW - Child
KW - Child, Preschool
KW - Diffuse Intrinsic Pontine Glioma/mortality
KW - Glioma/radiotherapy
KW - Humans
KW - Infusions, Intralesional
KW - Oncolytic Virotherapy/adverse effects
KW - Oncolytic Viruses
KW - Quality of Life
KW - Tumor Microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85133147520&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2202028
DO - 10.1056/NEJMoa2202028
M3 - Article
C2 - 35767439
SN - 0028-4793
VL - 386
SP - 2471
EP - 2481
JO - The New England journal of medicine
JF - The New England journal of medicine
IS - 26
ER -