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An infallible hand-held probe to aid cancer surgery

Jun 30, 2017   |   Polytechnique Montréal

[Release courtesy of Polytechnique Montréal]

Canadian researchers have invented an intraoperative probe that reliably detects multiple types of tumour cells

Patients with common widespread forms of cancer will enjoy longer life expectancy and reduced risk of recurrence thanks to a multimodal optical spectroscopy probe developed by Canadian researchers.

In 2015, scientists at Polytechnique Montréal, the University of Montreal Hospital Research Center (CRCHUM), the Montreal Neurological Institute and Hospital (The Neuro), McGill University, and the MUHC developed a hand-held Raman spectroscopy probe allowing surgeons to accurately detect virtually all brain cancer cells in real time during surgery.

The research team has now perfected the invention and designed a new device with improved accuracy, sensitivity and specificity, capable of detecting not only brain cancer cells but colon, lung and skin cancer cells as well. In intraoperative testing, the multimodal optical spectroscopy probe detected cancer cells infallibly, with nearly 100 per cent sensitivity—in other words, when pointed at a cancerous region, the probe is never wrong.

This breakthrough, details of which were published on June 28 in the American Association for Cancer Research journal Cancer Research, is the outcome of collaborative efforts between engineer Frédéric Leblond and neurosurgical oncology specialist Dr. Kevin Petrecca.

Lead author Michael Jermyn
Michael Jermyn, Visiting Research Scientist
, works in Professor Brian Pogue's lab and is the study's lead author.

“Minimizing, or completely eliminating, the number of cancer cells during surgery is a critical part of cancer treatment, yet detecting cancer cells during surgery is challenging,” explains Dr. Petrecca, who is Chief of Neurosurgery, a brain cancer researcher, and holder of the William Feindel Chair in Neuro-Oncology at the Neuro. “Often it is impossible to visually distinguish cancer from normal brain, so invasive brain cancer cells frequently remain after surgery, leading to cancer recurrence and a worse prognosis. Surgically minimizing the number of cancer cells improves patient outcomes.”

Dr. Frédéric Leblond, Professor of Engineering Physics at Polytechnique Montréal and a research fellow at the University of Montreal Hospital Research Centre (CRCHUM) [as well as Adjunct Associate Professor of Engineering at Dartmouth], notes: “The probe we’ve designed enables detection of nearly 100 per cent of cancer cells in the brain. This is a very important advance. We’ve also been able to demonstrate the effectiveness of our technology in treating other forms of cancer. This means that more patients will benefit from better diagnosis, more effective treatment, and lower risk of recurrence.”

The major advantage of this system is that surgeons can use it during a procedure to detect cancer cells in real time—a determination that is difficult to make via naked-eye observation.

“A technology with extremely high accuracy is necessary, since surgeons will be using this information to help determine if tissues contain cancer cells or not. An important feature of this device is its broad applicability. We found that it effectively detects multiple cancer types, including brain, lung, colon, and skin cancers,” Dr. Petrecca concludes.

Probe combines multiple technology modalities

The intraoperative probe developed in the laboratories uses the same Raman spectroscopy technology as the researchers’ first-generation probe to interpret the chemical composition of the tissue examined. First developed in 2015 and tested on more than 80 patients during surgery, the probe has now been perfected by its inventors. The new version is multimodal, also using intrinsic fluorescence spectroscopy to interpret the metabolic composition of the cells, as well as diffuse reflectance spectroscopy to analyze intrinsic tissue absorption in patients.

During recent testing on 15 other brain surgery patients, sequential use of these high-sensitivity spectroscopy techniques—integrated into a single sensor coupled with a detection system, in combination with stimulating lasers, a highly sensitive camera, and a spectrometer—the surgeon benefited from molecular imaging that provided never-before-seen accuracy, with cancer detection sensitivity improved by about 10 per cent compared with the first-generation probe.

Clinical trial under way

The first-generation Raman spectroscopy probe is currently the subject of a randomized controlled trial involving patients with gliomas. The study will be the first in the world to demonstrate the clinical benefits of intraoperative probe use during brain surgery. The results will be used to establish the protocol for an upcoming clinical trial of the second-generation multimodal probe.

In 2015, Dr. Petrecca and Professor Leblond created a company, ODS Medical, to commercialize the probe. They have since initiated the formal approval process with the U.S. Food and Drug Administration (FDA), to ensure transfer of the technology to hospital settings within a few years.

About the study

The article reporting on the study, “Highly accurate detection of cancer in situ with intraoperative, label-free, multimodal optical spectroscopy,” was published in the American Association for Cancer Research journal Cancer Research on June 28, 2017. The work was supported by the Fonds de recherche du Québec–Nature et technologies, the Natural Sciences and Engineering Research Council of Canada, Collaborative Health Research Projects (CIHR and NSERC), the Groupe de recherche en sciences et technologies biomédicales, and National Bank of Canada. The authors are Michael Jermyn [Visiting Research Scientist at Thayer School of Engineering at Dartmouth], Jeanne Mercier, Kelly Aubertin, Joannie Desroches, Kirk Urmey, Jason Karamchandiani, Eric Marple, Marie-Christine Guiot, Frederic Leblond, and Kevin Petrecca.

Link to source:

http://www.polymtl.ca/salle-de-presse/en/newsreleases/infallible-hand-held-probe-aid-cancer-surgery

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