DETERMINING RISK FOR PANCREATIC CANCER

In the latest clinical trial for a technique to detect pancreatic cancer, researchers found they could differentiate cells that are cancerous from those that are benign, pre-cancerous, or even early stage indicators called mucinous cystic lesions.

Pancreatic cancer, unseen at its earliest stages by any other method, can be detected by examining tissue from inside the duodenum, the uppermost section of the small intestine. The pancreatic duct communicates with the duodenum via the Ampulla of Vater. Researchers have shown that cells in a roughly 3 cm radius from this feature can show signs of the presence of cancer. Credit: Zina Deretsky, National Science Foundation
Pancreatic cancer, unseen at its earliest stages by any other method, can be detected by examining tissue from inside the duodenum, the uppermost section of the small intestine. The pancreatic duct communicates with the duodenum via the Ampulla of Vater. Researchers have shown that cells in a roughly 3 cm radius from this feature can show signs of the presence of cancer. Credit: Zina Deretsky, National Science Foundation


Pancreatic cancer is dangerous to screen for, yet deadly if ignored. The pancreas is extremely sensitive–biopsies can lead to potentially fatal complications–but with few symptoms, the cancer is usually detected too late.

The disease is the fourth largest cause of cancer-related deaths in the United States, with a five-year survival rate of less than 5 percent. If doctors can find ways to identify early precursor lesions, the disease can be prevented in most individuals.

Reporting online Feb. 10, 2009, in the journal Disease Markers, researchers from Northwestern University and Evanston Northwestern Healthcare report convincing results with their minimally invasive methods for detecting pancreatic cancer.

“This technique allows us to detect changes in cells that look normal using microscopy,” says co-author Vadim Backman of Northwestern University. “This level of detail allows us to detect cancer in its earliest stages.”

Their techniques, called four-dimensional elastic light scattering fingerprinting (4D-ELF) and low-coherence enhanced backscattering spectroscopy (LEBS), identify the cancer and its precursors by analyzing light reflected off cells in the duodenum, a section of the small intestine adjacent to the pancreas.

“I’m excited about this work,” said Leon Esterowitz, the National Science Foundation (NSF) biophotonics program director who helped fund this study and the development of the 4D-ELF and LEBS technologies. “I believe these results are very promising, and the techniques have a high probability of success for not just detecting early pancreatic cancer, but pre-cancer, so doctors can go ahead and treat the patient while there’s still a chance to defeat the disease.” Esterowitz added. “For pancreatic cancer, this could lead to not only an excellent prognosis, but perhaps even a cure.”

While earlier success had shown that the techniques could tell cancerous from non-cancerous tissue without resorting to a biopsy, the new study of 203 individuals was the first to show the method can identify various disease stages and risk factors, including a possible signature related to “family history.”

The researchers’ approach had a sensitivity of 95 percent for determining healthy tissue from cancerous tissue and appears to be the most successful yet developed for detecting pancreatic diseases at curable stages and for identifying high-risk individuals.

“These optical techniques have shown promise for detecting both colon and pancreatic cancer,” says Backman. “Our hope is to continue to test the ability to detect other forms of cancer, which would greatly expand the impact of the technology.” In ongoing work, the researchers will continue to refine their instrumentation and hope to validate the recent findings with further clinical trials.

This research was funded with NSF grant CBET-0733868, in addition to support from the V Foundation, the Rolfe Foundation and the National Institutes of Health.

Source: North Western University

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One thought on “DETERMINING RISK FOR PANCREATIC CANCER

  1. lisa caprise

    patient in tampa suffering 3 years with what feels like an arrow stuck in my body where my pancreas is and several trips to ER with pancreatic attacks feeling like something in that area would burst, still no clear diagnosi, just one lone dr who came to my room one night and forewarned me that 3-5 years from now i cold be facing pancreatic cancer. my veins in upper extremities collapse when pterced or form superficial clots, veins are also over sensitive, pain in the left flank, front and back area are constant and chronic since provocoked DVTs and PE back in 12/08. my body or life hasn’t been the same since. thnx for sharing this info. troubled in tampa, lisa caprise

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