A phase I/II clinical trial by researchers at Stanford University suggests that vaccines prepared from a patient's own tumour cells may prevent the incurable blood cancer mantle cell lymphoma (MCL) from returning after treatment.
The study, which will be published in the Journal of Experimental Medicine (JEM), reveals that the vaccines are a safe and effective way to induce the body's immune system to attack any tumour cells that could cause disease relapse.
MCL is an aggressive form of non-Hodgkin lymphoma in which white blood cells known as B cells become cancerous and form tumours in the lymph nodes and other parts of the body.
The disease is generally treated with a combination of chemotherapy and immunotherapy, often accompanied by a haematopoietic stem cell transplant to restore the body's ability to form normal, healthy blood cells.
But the cancer usually returns, and the average survival time for MCL patients is 5-7 years.
Ronald Levy and colleagues at Stanford University previously developed a tumour cell-based vaccine that prevents lymphomas from recurring in mice.
Tumour cells isolated from the mice are loaded with CpG oligonucleotides, short fragments of DNA that mimic bacterial DNA and can prompt an immune response against the cells when they are injected back into the mice.
"Guided by these preclinical results, we designed a phase I/II clinical trial (NCT00490529) to evaluate the therapeutic potential of a similar vaccination approach as an additive to standard stem cell transplantation for patients with MCL," Levy says.
In the trial, 47 MCL patients who had achieved remission through standard immune- and chemotherapies were vaccinated with their own, CpG-loaded, tumour cells.
The patients' immune cells were then collected and saved while the patients received a stem cell transplant.
Finally, the immune cells were transferred back into the patients, who were then monitored for signs of their MCL returning.
The vaccination regimen appeared to be safe, causing no side effects beyond those normally associated with stem cell transplants.
Over the following year, 89% of the patients remained free of minimal residual disease (MRD), meaning that their blood contained too few cancer cells to form any new tumours.
"That surpasses previously reported MRD-free rates for MCL patients," Levy says.
Of the patients, 40% formed immune cells capable of directly attacking and killing cancer cells.
These patients appeared to be especially well protected from disease relapse, going much longer without any recurrence of MCL, even if their tumours contained genetic mutations associated with a poor prognosis.
"Overall, our data demonstrate that the addition of a CpG-activated whole cell tumour vaccination followed by adoptive transfer of vaccine-primed immune cells to the treatment of MCL is feasible, safe, and can induce immune responses that are associated with a superior clinical outcome," Levy says.
The researchers are now considering ways to improve the immune response to tumour cell vaccination still further.
Source: Rockefeller University Press
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