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Phase Ib Clinical Trial of IGV-001 for Patients with Newly Diagnosed Glioblastoma.

Authors :
Andrews DW
Judy KD
Scott CB
Garcia S
Harshyne LA
Kenyon L
Talekar K
Flanders A
Atsina KB
Kim L
Martinez N
Shi W
Werner-Wasik M
Liu H
Prosniak M
Curtis M
Kean R
Ye DY
Bongiorno E
Sauma S
Exley MA
Pigott K
Hooper DC
Source :
Clinical cancer research : an official journal of the American Association for Cancer Research [Clin Cancer Res] 2021 Apr 01; Vol. 27 (7), pp. 1912-1922. Date of Electronic Publication: 2021 Jan 26.
Publication Year :
2021

Abstract

Purpose: Despite standard of care (SOC) established by Stupp, glioblastoma remains a uniformly poor prognosis. We evaluated IGV-001, which combines autologous glioblastoma tumor cells and an antisense oligonucleotide against IGF type 1 receptor (IMV-001), in newly diagnosed glioblastoma.<br />Patients and Methods: This open-label protocol was approved by the Institutional Review Board at Thomas Jefferson University. Tumor cells collected during resection were treated ex vivo with IMV-001, encapsulated in biodiffusion chambers with additional IMV-001, irradiated, then implanted in abdominal acceptor sites. Patients were randomized to four exposure levels, and SOC was initiated 4-6 weeks later. On the basis of clinical improvements, randomization was halted after patient 23, and subsequent patients received only the highest exposure. Safety and tumor progression were primary and secondary objectives, respectively. Time-to-event outcomes were compared with the SOC arms of published studies.<br />Results: Thirty-three patients were enrolled, and median follow-up was 3.1 years. Six patients had adverse events (grade ≤3) possibly related to IGV-001. Median progression-free survival (PFS) was 9.8 months in the intent-to-treat population (vs. SOC, 6.5 months; P = 0.0003). In IGV-001-treated patients who met Stupp-eligible criteria, PFS was 11.6 months overall ( n = 22; P = 0.001) and 17.1 months at the highest exposure ( n = 10; P = 0.0025). The greatest overall survival was observed in Stupp-eligible patients receiving the highest exposure (median, 38.2 months; P = 0.044). Stupp-eligible patients with methylated O <superscript>6</superscript> -methylguanine-DNA methyltransferase promoter ( n = 10) demonstrated median PFS of 38.4 months ( P = 0.0008). Evidence of immune activation was noted.<br />Conclusions: IGV-001 was well tolerated, PFS compared favorably with SOC, and evidence suggested an immune-mediated mechanism (ClinicalTrials.gov: NCT02507583).<br /> (©2021 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1557-3265
Volume :
27
Issue :
7
Database :
MEDLINE
Journal :
Clinical cancer research : an official journal of the American Association for Cancer Research
Publication Type :
Academic Journal
Accession number :
33500356
Full Text :
https://doi.org/10.1158/1078-0432.CCR-20-3805