Potential new tool against aggressive brain cancer

Updated on 25 July 2012

NBTI researchers study vaccine made from a patient's own blood cells as a potential weapon against aggressive brain cancer

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New hope for brain tumor: White blood cell vaccine

Singapore: Researchers at the Northwestern Brain Tumor Institute (NBTI) are trying to understand if a vaccine made from patient's own blood cells may slow the growth of a type of brain tumor. The national glioblastoma clinical trial is studying the vaccine's effect on glioblastoma multiformes (GBM), the most common and aggressive type of primary brain tumor.

The trial is an example of a growing trend in cancer research that seeks to understand if vaccines can be used to turn a person's own immune system into a weapon against cancers by slowing the growth of tumors.

Dr James Chandler, principal investigator and co-director, NBTI, and surgical director of neuro-oncology at Northwestern Memorial Hospital, said that, "Glioblastomas are complicated to treat because they are aggressive, fast-growing tumors that are often resistant to standard treatment. In this trial, a vaccine is made using the person's own white blood cells, which we hope will have the power to stimulate an immune response to kill brain tumor cells."

The vaccine, called ICT-107, is created by collecting the participant's white blood cells through a process called apheresis, which separates the components in the blood. The white blood cells are then treated to recognize the tumor cells turning them into immune cells, which early research indicates may be able to recognize and attack the tumor cells. Patients receive the vaccine in addition to standard treatment.

The phase II trial will examine both safety and efficacy of the ICT-107 vaccine. Researchers seek to enroll approximately 225 participants nationally who are newly diagnosed with a GBM. To be considered for enrollment, a person must be 18 years or older and not have a recurrent disease or any other active malignancy or history of malignancy. They must have undergone surgery to excise the GBM, but have not yet started chemotherapy or radiation.

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ShanmugaPriya Rajan 25 July 2012 at 11 PM

Can you elaborate the results/current scenario of the active participant.

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Saptarshi Chaudhuri (BioSpectrum)) Thu Jul 26 at 11 AM

Thank you for your comment. Glioblastoma multiformes (GBM) are typically treated with surgical resection followed by chemotherapy and radiation treatment. GBM tumors are extremely fast-growing and are often resistant to treatment. During the phase I clinical study of ICT-107 (a vaccine made from the patients' own white blood cells) in the treatment of GBM, 16 newly diagnosed patients who received the vaccine in addition to standard of care treatment of surgery, radiation and chemotherapy; demonstrated two-year overall survival of 80 percent and a three-year overall survival of 55 percent. The statistics compare favorably to the present 26 percent two-year overall survival and 16 percent three-year overall survival that is based on the historical standard of care treatment alone. Updated data from the 16 patients, who participated in the phase I trial, shows that the patients reported overall survival of 50 percent after four years and 38 percent of the patients were progression free (PFS) for 48-66 months. This compares very favorably to the historic mean OS of 12.1 percent after four years and 5.6 percent PFS after 48 months with standard of care alone. These are extremely positive figures. Lets hope that the trials of ICT-107 progress swiftly to the commercialization stage so that several lives could be saved from the menace of brain tumor. Do keep reading BioSpectrum Asia to get further insights into the world of Life Sciences.

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