Blood test monitors cancer treatment outcomes in real time

Cancer patients who are undergoing targeted therapy can look forward to a new blood test that could tell their doctors whether the treatment is working, within one day after the start of the treatment. This should significantly speed up the evaluation process and enable doctors to make adjustments to the treatment plan, if necessary, to improve patients’ chances of recovery.

Unlike conventional chemotherapies that interfere with all rapidly dividing cells and can cause widespread damage to cells, targeted medicines attack specific molecules that instruct cancer cells to grow and spread, and in turn, block the abnormal growth of the cancer. Despite the specific nature of targeted drugs, current clinical evaluation of their treatment in solid tumours primarily relies on either tumour volumetric imaging, which is insensitive and delayed, or invasive tissue biopsies.

Assistant Professor Shao Huilin and her research team from the Department of Biomedical Engineering and Institute for Health Innovation & Technology (iHealthtech) at the National University of Singapore (NUS) have now developed a technology that is less invasive and significantly brings forward the evaluation window. Their technique, termed extracellular vesicle monitoring of small-molecule chemical occupancy and protein expression (ExoSCOPE) and described in the journal Nature Nanotechnology, takes advantage of extracellular vesicles (EVs) secreted by cancer cells and circulating in blood as a reflective indicator of drug effectiveness in solid tumours.

“Conventional procedures such as tumour imaging are not only expensive but also delayed. For these methods, treatment effectiveness can only be determined after weeks,” Asst Prof Shao said. “Using the ExoSCOPE, we can directly measure the outcomes of drug effectiveness within 24 hours of treatment initiation. This will significantly reduce the time and cost for cancer treatment monitoring.

“This method requires only a tiny amount of blood sample for the analysis and each test takes less than one hour to complete, so it is less invasive and yet more informative. In this way, doctors could monitor a patient’s response to treatment more regularly during the course of the treatment and make timely adjustments to customise the treatment for better outcomes.”

To achieve sensitive and rapid analysis of drug efficacy through blood samples, the NUS team developed the ExoSCOPE as an integrated nanotechnology platform. It measures EVs, which are membrane vesicles of dimension at least a hundred times smaller than the diameter of human hair and invisible under conventional light microscopy.

During successful cancer treatment, when a targeted cancer drug attaches to a cancer cell and interferes with tumour growth, the treated cell will release into the bloodstream EVs containing the drug. The ExoSCOPE platform harnesses a complementary approach of chemical biology and sensor development to measure these delicate drug changes in EVs.

“Current technologies to measure drug–target interactions require complex processing and invasive tissue biopsies, limiting their clinical utility for cancer treatment monitoring,” said Dr Sijun Pan, Research Fellow from iHealthtech and co-first author of the study. “By using specially designed chemical probes, our platform is highly sensitive in capturing and labelling EVs in a small blood sample in order to assess drug–target interactions.”

“The ExoSCOPE sensor contains millions of gold nanorings to capture the EVs and amplify their drug labelling signals to induce strong light signals,” added Zhang Yan, a doctoral student from Department of Biomedical Engineering and iHealthtech and co-first author of the study. “These light signals are then processed to give a readout to indicate drug effectiveness.”

Using the ExoSCOPE platform, the team collected information on different types of EVs and their drug changes, when treated with various targeted therapies. The platform not only identifies cancer-released EVs, it also monitors their drug dynamics over time to accurately distinguish treatment sensitivity and resistance.

“Existing blood pharmacokinetic or pharmacodynamic approaches measure the total drug concentration in blood,” Asst Prof Shao said. “This ensemble information does not reflect drug efficacy in tumours. The ExoSCOPE, however, measures drug changes in cancer-released EVs to accurately reflect tumour treatment responses.”

In a clinical trial involving 163 blood samples from 106 patients, the ExoSCOPE has shown encouraging results on lung cancer patients to enable timely evaluation of patients’ targeted treatment outcomes. Compared against the gold standard of tumour volumetric imaging, which was performed at the end of the entire treatment regimen, the ExoSCOPE achieved an accuracy rate of 95%, within 24 hours of treatment initiation. The technique’s high analytical performance thus paves the way for the use of bloodborne EVs for monitoring different interactions between drugs and protein targets in the human body.

“The ExoSCOPE presents a paradigm shift in blood-based drug evaluation for targeted drug selection and real-time treatment monitoring,” Asst Prof Shao said. “The technique can also empower the clinical community to make more timely treatment decisions.”

The nine-member NUS team took two years to develop and validate the ExoSCOPE platform. Their next challenge is to expand the platform to measure the efficacy of different drugs and apply the technology to a spectrum of diseases from cancers to cardiovascular and neurological disease. A patent has been filed for ExoSCOPE and the NUS team hopes to bring this technology to market in the next three years.

“I hope our technology can contribute towards personalised treatment, to guide the selection, dosage and duration of different treatments, and improve treatment outcomes,” Asst Prof Shao said.

Image caption: Assistant Professor Shao Huilin (left), Dr Sijun Pan (right) and their team have developed ExoSCOPE, a blood test that measures the effectiveness of cancer treatment within 24 hours after treatment initiation.

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