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. 2022 Nov 14;24(Suppl 7):vii66. doi: 10.1093/neuonc/noac209.259

CTIM-27. AUTOLOGOUS TUMOR LYSATE-LOADED DENDRITIC CELL VACCINATION IMPROVES SURVIVAL IN PATIENTS WITH NEWLY DIAGNOSED AND RECURRENT GLIOBLASTOMA: SURVIVAL RESULTS FROM A PHASE 3 TRIAL

Linda M Liau 1, Keyoumars Ashkan 2, Steven Brem 3, Jian Campian 4, John Trusheim 5, Fabio Iwamoto 6, David Tran 7, George Anstass 8, Charles Cobbs 9, Jason Heth 10, Michael Salacz 11, Stacy D'Andre 12, Robert Aiken 13, Yaron Moshel 14, JooYeon Nam 15, Clement Pillainayagam 16, Stephanie Wagner 17, Kevin Walter 18, Rekha Chaudary 19, Samuel Goldlust 20, Ian Lee 21, Daniela Bota 22, Heinrich Elinzano 23, Jai Grewal 24, Kevin Lillehei 25, Tom Mikkelsen 26, Tobias Walbert 27, Steve Abram 28, Andrew Brenner 29, Matthew Ewend 30, Simon Khagi 31, Darren Lovick 32, Jana Portnow 33, Lyndon Kim 34, William Loudon 35, Nina Martinez 36, Reid Thompson 37, David Avigan 38, Karen Fink 39, Francois Geoffroy 40, Pierre Giglio 41, Oleg Gligich 42, Dietmar Krex 43, Scott M Lindhorst 44, Jose Lutzky 45, Hans-Joerg Meisel 46, Minou Nadji-Ohl 47, Lhagva Sanchin 48, Andrew Sloan 49, Marnix Bosch 50
PMCID: PMC9660964

Abstract

BACKGROUND

Standard of care (SOC) and patient survival in glioblastoma have changed little in the past 17 years. We evaluated in a phase 3 trial whether adding an autologous tumor lysate-loaded dendritic cell vaccine (murcidencel) to SOC extends survival. Patients and

METHODS

Newly diagnosed glioblastoma patients were randomized 2:1 to either murcidencel or placebo. Under a crossover design, all patients could receive murcidencel following tumor recurrence. All parties remained blinded regarding treatments before recurrence. Patients thus received murcidencel at new diagnosis (nGBM) or at recurrence (rGBM) following crossover from placebo. The primary and secondary endpoints compare overall survival (OS) with contemporaneous, matched external controls. Four sets of analyses were conducted to ensure rigorous matching of the controls, reduce biases, and confirm the robustness of the results.

RESULTS

331 patients were enrolled. With the crossover, 89% received murcidencel. Median OS (mOS) for nGBM patients (n = 232) was 19.3 months from randomization (22.4 months from surgery) with murcidencel vs. 16.5 months from randomization in the controls (HR = 0.80, p = 0.002). Survival at 48 months from randomization was 15.7% vs. 9.9%, and at 60 months was 13% vs. 5.7%. For rGBM (n = 64), mOS was 13.2 months from relapse vs. 7.8 months in the controls (HR = 0.58, p < 0.001). Survival at 24 months post-recurrence was 20.7% vs. 9.6%, and at 30 months post-recurrence was 11.1% vs 5.1%. In nGBM patients with methylated MGMT (n = 90), mOS was 30.2 months from randomization (33 months from surgery) with murcidencel vs. 21.3 months from randomization in the controls (HR = 0.74, p = 0.027). The treatment was well tolerated, with only 5 serious adverse events deemed at least possibly related to the vaccine.

CONCLUSION

Clinically meaningful and statistically significant survival extension was seen in both nGBM and rGBM patients treated with murcidencel and SOC compared with contemporaneous, matched external controls who received SOC alone.


Articles from Neuro-Oncology are provided here courtesy of Society for Neuro-Oncology and Oxford University Press

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