First results on survival from a large Phase 3 clinical trial of an autologous dendritic cell vaccine in newly diagnosed glioblastoma

Author:

Liau Linda M.,Ashkan Keyoumars,Tran David D.,Campian Jian L.,Trusheim John E.,Cobbs Charles S.,Heth Jason A.,Salacz Michael,Taylor Sarah,D’Andre Stacy D.,Iwamoto Fabio M.,Dropcho Edward J.,Moshel Yaron A.,Walter Kevin A.,Pillainayagam Clement P.,Aiken Robert,Chaudhary Rekha,Goldlust Samuel A.,Bota Daniela A.,Duic Paul,Grewal Jai,Elinzano Heinrich,Toms Steven A.,Lillehei Kevin O.,Mikkelsen Tom,Walbert Tobias,Abram Steven R.,Brenner Andrew J.,Brem Steven,Ewend Matthew G.,Khagi Simon,Portnow Jana,Kim Lyndon J.,Loudon William G.,Thompson Reid C.,Avigan David E.,Fink Karen L.,Geoffroy Francois J.,Lindhorst Scott,Lutzky Jose,Sloan Andrew E.,Schackert Gabriele,Krex Dietmar,Meisel Hans-Jorg,Wu Julian,Davis Raphael P.,Duma Christopher,Etame Arnold B.,Mathieu David,Kesari Santosh,Piccioni David,Westphal Manfred,Baskin David S.,New Pamela Z.,Lacroix Michel,May Sven-Axel,Pluard Timothy J.,Tse Victor,Green Richard M.,Villano John L.,Pearlman Michael,Petrecca Kevin,Schulder Michael,Taylor Lynne P.,Maida Anthony E.,Prins Robert M.,Cloughesy Timothy F.,Mulholland Paul,Bosch Marnix L.ORCID

Abstract

Abstract Background Standard therapy for glioblastoma includes surgery, radiotherapy, and temozolomide. This Phase 3 trial evaluates the addition of an autologous tumor lysate-pulsed dendritic cell vaccine (DCVax®-L) to standard therapy for newly diagnosed glioblastoma. Methods After surgery and chemoradiotherapy, patients were randomized (2:1) to receive temozolomide plus DCVax-L (n = 232) or temozolomide and placebo (n = 99). Following recurrence, all patients were allowed to receive DCVax-L, without unblinding. The primary endpoint was progression free survival (PFS); the secondary endpoint was overall survival (OS). Results For the intent-to-treat (ITT) population (n = 331), median OS (mOS) was 23.1 months from surgery. Because of the cross-over trial design, nearly 90% of the ITT population received DCVax-L. For patients with methylated MGMT (n = 131), mOS was 34.7 months from surgery, with a 3-year survival of 46.4%. As of this analysis, 223 patients are ≥ 30 months past their surgery date; 67 of these (30.0%) have lived ≥ 30 months and have a Kaplan-Meier (KM)-derived mOS of 46.5 months. 182 patients are ≥ 36 months past surgery; 44 of these (24.2%) have lived ≥ 36 months and have a KM-derived mOS of 88.2 months. A population of extended survivors (n = 100) with mOS of 40.5 months, not explained by known prognostic factors, will be analyzed further. Only 2.1% of ITT patients (n = 7) had a grade 3 or 4 adverse event that was deemed at least possibly related to the vaccine. Overall adverse events with DCVax were comparable to standard therapy alone. Conclusions Addition of DCVax-L to standard therapy is feasible and safe in glioblastoma patients, and may extend survival. Trial registration Funded by Northwest Biotherapeutics; Clinicaltrials.gov number: NCT00045968; https://clinicaltrials.gov/ct2/show/NCT00045968?term=NCT00045968&rank=1; initially registered 19 September 2002

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

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