Findings Presented at the Society of Surgical Oncology Annual Cancer
Symposium
Northfield Laboratories Inc. (Nasdaq: NFLD) announced today that
researchers from the University of Colorado at Denver / Denver Health
Medical Center, Bonfils Blood Center in Denver, and University of Texas
Southwestern Medical Center at Dallas have demonstrated that the use of
Northfield’s human polymerized hemoglobin (PolyHeme®)
significantly reduces metastases and primary tumor growth in a mouse
model of pancreatic cancer. The authors suggest that the use of PolyHeme
in lieu of red blood cells may prolong survival in patients with
pancreatic cancer who require transfusions. The research is being
presented by Carlton C. Barnett, M.D., Director of Surgical Oncology at
Denver Health Medical Center, at the Society of Surgical Oncology 62nd
Annual Cancer Symposium, which begins today and continues through
Saturday in Phoenix, AZ.
As many as 80% of patients undergoing operation for pancreatic cancer
receive perioperative red blood cell transfusion. The literature
describes an association with decreased survival in these transfusion
recipients. Ernest E. “Gene” Moore, M.D., and colleagues previously
demonstrated that the plasma fraction of stored red blood cells contains
biologically active factors that cause immune dysfunction. Furthermore,
they demonstrated that PolyHeme is devoid of these factors and
attenuates the observed immune dysfunction. Dr. Barnett and his
colleagues have determined that elevations of some of these factors have
been associated with primary tumor progression and decreased survival in
a mouse model of pancreatic cancer. Based upon these findings, they
hypothesized that infusion of PolyHeme in lieu of red blood cells might
mitigate the adverse affects of blood transfusion on pancreatic cancer
progression.
This study compared the outcome of treatment with PolyHeme or plasma
from stored red blood cells in a mouse model of pancreatic cancer.
PolyHeme did not demonstrate the elevated levels of biologically active
factors observed in the plasma from stored red blood cells. Furthermore,
metastases and primary tumor growth were significantly reduced in
animals receiving PolyHeme compared to animals receiving plasma from
stored red blood cells.