Personalized cancer vaccine may increase long-term survival in patients with deadly brain cancer
An international Phase III study led by researchers at UCLA and at Northwest Biotherapeutics, Inc. has found that a personalized glioblastoma vaccine may increase long-term survival in some patients. Nearly 30 percent of patients in the current trial have now survived at least three years post-enrollment, with patients continuing to be followed over time.
The vaccine, known as DCVax-L, uses a patient’s own dendritic cells to help activate the immune system to fight cancer. Currently, median survival for glioblastoma is 15 to 17 months, and less than 5 percent of glioblastoma patients who receive standard care survive five years.
The interim findings from the study, which is still in progress, were published May 29 in the Journal of Translational Medicine. The study is the largest trial to date testing a customized vaccine in patients diagnosed with the deadly brain cancer.
“The survival rate is quite remarkable compared to what would be expected for glioblastoma,” said lead author Dr. Linda Liau, chair of the neurosurgery department at the David Geffen School of Medicine at UCLA and a member of the UCLA Jonsson Comprehensive Cancer Center. “What’s particularly impressive about immunotherapy trials is that there seems to be a population of about 20 to 30 percent of patients who are living significantly longer than expected – the long tail of the survival curve. And those are the people in whom we think there may be a particularly strong immune response against their cancer that is protecting them from getting tumor reoccurrence.”
The vaccine was administered in newly diagnosed glioblastoma patients -- at 80 sites across the globe -- from July 2007 through November 2015. All patients underwent standard care therapy (surgery to resect the tumor, followed by chemoradiotherapy) before participating in the trial.
After standard care therapy, patients were randomized into two arms of the trial. The first group (232 patients) continued to receive standard care and DCVax-L; the second group (99 patients) received standard care and a placebo treatment. All patients were allowed to receive the vaccine following tumor progression or recurrence. Due to the crossover design of the trial, nearly 90 percent of the patients received the vaccine.
Researchers found that when analyzing all the patients in both arms of the trial (i.e., the intent to treat population), median survival is 23.1 months, which is eight months longer than the current median survival time from historical studies using standard of care chemoradiation alone.
Of those who were enrolled more than three years before the data analysis date of this publication, 67 patients (30 percent of the total) survived for more than 30 months, and 44 (24.2 percent) survived for more than 36 months. These patients are expected to have a median survival of 46.5 to 88.2 months. At the time of the analysis, 108 of the 331 patients enrolled in the trial (32.6 percent) were still alive.
Researchers at UCLA have spent almost two decades working to activate dendritic cells against brain cancer. Dendritic cells are a type of white blood cell that typically alerts the immune system when it detects a foreign invader. Liau and her team were the first to test a dendritic cell-based vaccine in patients with glioblastoma, a type of tumor that had previously been thought to be immune-privileged, meaning the immune system won’t attack it. However, Liau and her colleagues were able to demonstrate in previous studies that the body could actually mount an immune response against tumors in the brain following the vaccination.
“The unique thing about the DCVax-L vaccine is that this doesn’t target a single antigen,” Liau said. “This treatment actually uses the patient’s own tumor specimen to make the vaccine. This is really a form of personalized immunotherapy that is customized to an individual patient and his/her tumor.”
The vaccine works by combining brain tumor tissue lysate removed during a patient’s surgery with dendritic immune cells drawn from his or her blood. The dendritic cells are activated in the lab to turn against the tumor cells and then injected back into the patient, activating his or her T cells to attack the tumor. In short, the vaccine teaches the immune system to battle the cancer.
Because patients on the trial are living longer than what has been historically expected, the study groups are still blinded and researchers are continuing to monitor the patients to assess the ultimate difference in long-term survival. At that point, they’ll issue a final report.
Liau and her colleagues are also in the process of developing new therapies that combine the vaccine and other treatments, with new clinical trials expected to be open in the near future.
Research reported in the Journal of Translational Medicine was supported by Northwest Biotherapeutics, Inc. and the UCLA SPORE in Brain Cancer.
In addition to Liau, other UCLA Jonsson Comprehensive Cancer Center authors include: Dr. Robert M. Prins, professor in neurosurgery and molecular and medical pharmacology, and Timothy F. Cloughesy, professor in neurology and director of the neuro-oncology program at UCLA.