In an editorial in the current edition of the New England Journal of
Medicine, Henry T. Lynch, M.D., hereditary cancer expert and medical
oncologist at Creighton University, recommends physicians conduct genetic
screening tests for hereditary nonpolyposis colorectal cancer, also known as
the Lynch Syndrome, named for Dr. Lynch. Dr. Lynch is the holder of the
Charles F. and Mary C. Heider Endowed Chair in Cancer Research, professor of
medicine and chairman of Preventive Medicine at Creighton University.
The screening recommended is a microsatellite-instability (MSI) and
immunohistochemical molecular genetic staining test, which identifies the
absence of proteins that can protect against colorectal cancer, the third
most common cause of death from cancer in the U.S. As Dr. Lynch indicates in
his editorial, co-authored by his son, Patrick M. Lynch, J.D., M.D., a
gastroenterologist and associate professor of medicine a the University of
Texas M.D. Anderson Cancer Center in Houston, these tests are efficient and
economical ways to screen for the Lynch Syndrome, the most common of which
is colorectal cancer. The MSI screening test Dr. Lynch recommends can have a
strong impact on the families of patients who present with tumors in the
Lynch Syndrome by helping to identify family members who are at high risk
and who should have regular colonoscopies starting at age 25.
MSI and immunohistochemical tests are important because of their
significantly lower cost approximately $300 compared to the high cost
$2,000 to test for the germ-line-mutations that predispose patients to the
Lynch Syndrome, said Dr. Lynch. This diagnosis may then be fortified by a
well-orchestrated cancer family history.
According to Dr. Lynch, I want to encourage new thinking among physicians
about how to use molecular genetic information, along with the family
history in order to do a better job in identifying patients at risk for the
Lynch Syndrome so that we can then screen and manage them effectively for
various types of cancer. |