Fred Hutch is a world-leader in developing treatments for brain cancers that affect adults and children. Our researchers are:
Engineering stem cells to treat brain tumors – Dr. Hans-Peter Kiem and colleagues have developed a way to extract a brain cancer patient's blood stem cells and insert a special "resistance" gene designed to protect them from damage by common chemotherapy drugs, such as temozolomide and BCNU. Infusing these enhanced cells into patients could give them new hope against the most aggressive form of brain cancer—glioblastoma—which is very difficult to treat.
Addressing the molecular basis of brain tumors – Dr. Eric Holland and his colleagues are developing mouse models of brain cancer that mimic the behavior of the disease in patients and imaging strategies to follow tumors as they develop. These efforts have led to clinical trials for glioma patients. Learn more >
Boosting the effectiveness of brain tumor drugs – Drs. Patrick Paddison and Olson are searching for new targets for therapies that increase the effectiveness of anticancer drugs currently in clinical trials. Employing a new technology called RNA interference, Paddison's group is identifying genetic nodes that can be shut off to make brain tumor cells more vulnerable to existing treatments.
Collaborating to treat glioblastoma – The Olson lab is collaborating with Dr. Patrick Paddison, who has discovered a method for identifying genes that kill cancer cells while sparing normal cells. The team has identified two novel targets that killed glioblastoma cells while sparing neural stem cells. Now Fred Hutch is working with other leading organizations to identify drugs that affect the identified targets.
Developing therapies for untreated tumors – Traditionally, patients with a rare brain cancer called supratentorial primitive neuroectodermal tumors (sPNETs) have been grouped with patients suffering from another, more common malignant brain tumor: medulloblastoma. Although both brain tumors are treated with the same drug, survival rates in patients with sPNETs have not improved. The Olson lab, in partnership with Seattle Children's, is investigating whether current drugs may effectively treat sPNETs.
Improving drug delivery – The Olson lab has invented "porous needle array" technology that allows investigators to inject multiple drugs into a single solid tumor. The lab is using the technology to identify and prioritize drug combinations for pediatric brain tumor patients while pharmaceutical companies are using it to identify drugs that are more effective in combination than individually. The technology is being commercialized by Seattle-based Presage Biosciences.
Finding new uses for old drugs – Fred Hutch researchers have created the world's first patient-derived models for this solid tumor. After screening more than 700 possible targets for treatment, seven targets were identified for which drugs already exist. Those candidates are being used in mouse studies. Human clinical trials are expected to launch within three years.
Childhood brain tumors
Pursuing natural treatments – Dr. Olson and his colleagues have shown that a plant chemical known as cyclopamine stops the growth of the most common malignant childhood brain cancer, called medulloblastoma. These drugs block a specific pathway that is critical for medulloblastoma growth. They represent a first step toward replacing more toxic therapies. Learn more >
Working to improve medulloblastoma treatment – Hutch investigators recently completed a study that identified a drug known as IPI-926 that dramatically increases the survival of mice with medulloblastoma tumors, without chemotherapy and radiation. Investigators also discovered the drug is only effective in 15 to 20 percent of patients with mutations of a specific pathway in the brain. These discoveries will influence future national clinical trials of IPI-926.
Investigating treatments based on vitamin A – Dr. Olson and colleagues also found that drugs derived from vitamin A—known as retinoids—may be highly effective and minimally toxic treatments for medulloblastoma. Learn more >