The innovative device, which is the size and shape of a grain of rice, can perform hundreds of studies at the same time to examine the impact of novel treatments on some of the most difficult-to-treat brain tumours. Researchers from Brigham and Women’s Hospital, a founding member of the Mass General Brigham healthcare system, have created a device that can help in therapy testing in patients with gliomas, which are brain or spinal cord tumours.
The device, which is meant to be used during standard-of-care surgery, provides unique insight into the impact of drugs on glioma tumours in a phase 1 clinical trial with no adverse effects on patients.
Results from the pilot clinical trial for the device are published in Science Translational Medicine.
“In order to make the greatest impact on how we treat these tumours, we need to be able to understand, early on, which drug works best for any given patient,” said co-principal investigator and co-corresponding author Pierpaolo Peruzzi, MD, PhD, an assistant professor in the Department of Neurosurgery at Brigham and Women’s Hospital.
“The problem is that the tools that are currently available to answer this question are just not good enough. So we came up with the idea of making each patient their own lab, by using a device which can directly interrogate the living tumour and give us the information that we need.”
About 20,000 people in the US each year are diagnosed with gliomas, a type of tumour that affects the brain and spinal cord. Gliomas are also among the deadliest brain cancers and are notoriously difficult to treat.
One challenge in developing targeted therapies for glioma is that it can be difficult to test many different combinations of drugs in tumour cells because it’s only possible to treat patients with one approach at a time. This has been a significant barrier for hard-to-treat cancers like gliomas, for which combination therapies are a promising avenue.
Peruzzi worked closely with co-principal investigator Oliver Jonas, PhD, an associate professor in the Department of Radiology at Brigham, to develop a device that can work around some of the barriers to precision medicine in gliomas. These microdevices are implanted in a patient’s tumour during surgery and removed before the surgery is complete.
“It’s important that we are able to do this in a way that best captures the features of each patient’s tumour and, at the same time, is the least disruptive of the standard of care,” said Peruzzi. “This makes our approach easy to integrate into patients’ treatment and allows its use in real life.”
In the time the device is implanted—about 2-3 hours—it administers tiny doses of up to 20 drugs into extremely small areas of the patient’s brain tumour. The device is removed during the surgery and the surrounding tissue is returned to the lab for analysis.
Because the device works while the tumour is still in the body, conducting experiments this way gives the unparalleled ability to assess the effects of drugs on the tumour microenvironment, the cells immediately surrounding cancer cells that can make up almost half the mass of a tumour.
“This is not in the lab, and not in a petri dish,” said Peruzzi. “It’s actually in real patients in real-time, which gives us a whole new perspective on how these tumours respond to treatment.”
In the current study, the researchers tested their device on six patients undergoing brain surgery to remove a glioma tumour. None of the patients experienced any adverse effects from the device, and the researchers were able to collect valuable biological data from the devices, such as how the response changes based on drug concentrations, or what molecular changes each drug produces in the cells.
While the study demonstrated that the device was safe and could be easily incorporated into surgical practice, the researchers are still working on determining the exact ways the data it gathers should be used to optimize glioma therapy.
The researchers are currently conducting a two-stage version of their procedure in which patients receive the device through minimally invasive surgery 72 hours before their main surgery.
“We’re optimistic that this is a new generation approach for personalized medicine,” said Peruzzi. “The ability to bring the lab right to the patient unlocks so much potential in terms of the type of information we can gather, which is new and exciting territory for a disease that has very few options at present.”
This story has been published from a wire agency feed without modifications to the text. Only the headline has been changed.
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