Delivering Toca 5 data
11-22-2019
by DDNews Staff  |  Email the author

SHARING OPTIONS:

SAN DIEGO—Tocagen Inc. has just presented the full results from the Toca 5 Phase 3 trial evaluating Toca 511 & Toca FC in patients with recurrent high grade glioma (HGG) at the Society for Neuro-Oncology (SNO) Annual Meeting.
 
The data were presented on behalf of the Toca 5 clinical investigators by Timothy Cloughesy, M.D., professor of Neurology and director of the Neuro-Oncology program at the University of California, Los Angeles and principal investigator for the Toca 5 trial.
 
Toca 5 was a Phase 3 randomized trial of Toca 511 & Toca FC in patients with recurrent HGG, undergoing resection. The trial involved 67 sites globally and enrolled 403 patients. Patients were randomized 1:1 prior to surgical resection to receive either the Toca 511 & Toca FC regimen or the standard of care (SOC) treatment (lomustine, temozolomide or bevacizumab).
 
The primary endpoint of the trial was overall survival (OS). Secondary endpoints included durable response rate, durable clinical benefit rate, duration of durable response and overall survival at 12 months. Patients were stratified based on IDH1 mutation status, KPS and geographic region. The baseline demographics and disease characteristics of the study were well balanced in the intent to treat populations and the 26 pre-specified subgroups.
 
As previously announced, the trial did not meet either the primary or secondary endpoints. The safety, tolerability and adverse event profile of Toca 511 & Toca FC was as expected for this patient population. In the ITT population, the median number of cycles of Toca FC was two and the median number of cycles across the SOC options ranged from two to four.
 
In a pre-planned subgroup analysis, subjects with second recurrence (N=60) showed a 57% risk reduction for death when treated with Toca 511 and Toca FC (21.82 months median OS, compared to 11.14 months), representing an approximate doubling of survival. Further analysis of the second recurrence subgroup showed that patients with IDH1 mutations and anaplastic astrocytoma (AA) had the greatest survival benefit. Second recurrence patients with IDH1 mutations and AA received a median of six cycles of Toca FC, compared to a median of three cycles across the SOC options.
 
“The positive outcome for patients at second recurrence in the Toca 5 trial are compelling, despite the disappointment of the overall trial results,” said Cloughesy. “Combined with an acceptable safety profile, these data support a potential opportunity to address the high unmet needs of this well-defined patient population and should inform any future development of the Toca 511 & Toca FC regimen.”
 
Molecular data from the Toca 5 trial were presented by Michael A. Vogelbaum, M.D., Ph.D., program leader of Neuro-Oncology and chief of Neurosurgery at the Moffitt Cancer Center, at the Society for Neuro-Oncology and Society for CNS Interstitial Delivery of Therapeutics’ 3rd Joint Conference on Therapeutic Delivery to the CNS.
 
Data indicated that the immunological profile at baseline was well balanced between the two arms of the trial. Data also showed that patients in the second recurrence, IDH1 mutations and AA subgroups had a more robust immune profile prior to treatment. These data suggest that patients within these subgroups may have been favorably predisposed to generate anti-tumor immune responses.
 
“We have conducted a thorough analysis of the Toca 5 data and a subgroup of patients appear to benefit from treatment with Toca 511 & Toca FC. We have submitted the data to the FDA and anticipate providing an update once we have more clarity on potential next steps for our recurrent brain cancer program in the coming months,” added Marty Duvall, chief executive officer of Tocagen.
 
Copies of the presentations by Cloughesy and Vogelbaum are available here.
Code: E11221901

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