A new microscope can give surgeons real-time pathology data to guide cancer-removal surgeries and can also non-destructively examine tumor biopsies in 3D.
When women undergo lumpectomies to remove breast cancer, doctors try to remove all the cancerous tissue while conserving as much of the healthy breast tissue as possible.
But currently there’s no reliable way to determine during surgery whether the excised tissue is completely cancer-free at its margins — the proof that doctors need to be confident that they removed all of the tumor. It can take several days for pathologists using conventional methods to process and analyze the tissue.
That’s why between 20 and 40 percent of women have to undergo second, third, or even fourth breast-conserving surgeries to remove cancerous cells that were missed during the initial procedure, according to studies.
Surgeons Flying Blind
The new microscope could help solve this, and other, problems. It can rapidly and non-destructively image the margins of large fresh tissue specimens with the same level of detail as traditional pathology — in no more than 30 minutes.
“Surgeons are sort of flying blind during these breast-conserving surgeries. Oftentimes they’ve left some tumor behind which they don’t know about until a few days later when the pathologist finds it.
If we can rapidly image the entire surface or margin of the excised tissue during the procedure, we can tell them if they still have tumor left in the body or not. And that would be a huge benefit to cancer patients,”
says Jonathan Liu, mechanical engineering professor at the University of Washington.
The new light-sheet microscope offers other advantages over existing processes and microscope technologies. It conserves valuable tissue for genetic testing and diagnosis, quickly and accurately images the irregular surfaces of large clinical specimens, and allows pathologists to zoom in and “see” biopsy samples in 3D.
“The tools we use in pathology have changed little over the past century. This light-sheet microscope represents a major advance for pathology and cancer patients, allowing us to examine tissue in minutes rather than days and to view it in three dimensions instead of two—which will ultimately lead to improved clinical care,”
says coauthor Nicholas Reder, chief resident and clinical research fellow in the department of pathology.
Open-top Light-sheet Microscopy
Current pathology techniques involve processing and staining tissue samples, embedding them in wax blocks, slicing them thinly, mounting them on slides, staining them, and then viewing these two-dimensional tissue sections with traditional microscopes — a process that can take days to yield results.
Another technique to provide real-time information during surgeries involves freezing and slicing the tissue for quick viewing. But the quality of those images is inconsistent, and certain fatty tissues, such as those from the breast, do not freeze well enough to reliably use the technique.
By contrast, the new open-top light-sheet microscope uses a sheet of light to optically “slice” through and image a tissue sample without destroying any of it.
All of the tissue is conserved for potential downstream molecular testing, which can yield additional valuable information about the nature of the cancer and lead to more effective treatment decisions.
“Slide-based pathology is still an analog technique, much like radiology was several decades ago when X-rays were obtained on film. By imaging tissues in 3D without having to mount thin tissue sections on glass slides, we are trying to transform pathology much like 3D X-ray CT has transformed radiology,” Liu says. “While it is possible to scan microscope slides for digital pathology, we digitally image the intact tissues and bypass the need to prepare slides, which is simpler, faster, and potentially less expensive.”
Coauthor Larry True, professor of pathology, adds:
“If we can do this without consuming any tissue, so much the better. We want to use that valuable tissue for purposes which are becoming ever more important for treating patients—such as sequencing the tumor cells and finding genetic abnormalities that we can target with specific drugs and other precision medicine techniques.”
The light-sheet microscope also offers advantages over other non-destructive optical-sectioning microscopes on the market today, which process images slowly and have difficulty maintaining the optimal focus when dealing with clinical specimens, which always have microscopic surface irregularities.
The new microscope can both image large tissue surfaces at high resolution and stitch together thousands of two-dimensional images per second to quickly create a 3D image of a surgical or biopsy specimen. That additional data could one day allow pathologists to more accurately and consistently diagnose and grade tumors.
“Pathologists are currently very limited in how much they can look at on a glass slide. If we can give them three-dimensional data, we can give them more information to help improve the accuracy of a patient’s diagnosis,”
says coauthor Adam Glaser, a postdoctoral fellow in the University of Washington’s Molecular Biophotonics Laboratory.
The team achieved these improvements by configuring various optical technologies in new ways and optimizing them for clinical use. Their open-top arrangement, which places all of the optics underneath a glass plate, allows them to image larger tissues than other microscopes.
The team is currently working on speeding up the optical-clearing process that allows light to penetrate biopsy samples more easily.
Future areas of research include optimizing their 3D immunostaining processes, as well as developing algorithms that can process the vast amounts of 3D pathology data that their system generates, with the ultimate goal of helping pathologists zero in on suspicious areas of tissue.
Adam K. Glaser, Nicholas P. Reder, Ye Chen, Erin F. McCarty, Chengbo Yin, Linpeng Wei, Yu Wang, Lawrence D. True & Jonathan T. C. Liu
Light-sheet microscopy for slide-free non-destructive pathology of large clinical specimens
Nature Biomedical Engineering 1, Article number: 0084 (2017) doi:10.1038/s41551-017-0084
Top Image: Mark Stone/University of Washington