Reuters Health Information: Chronic liver disease may boost risk of colorectal cancer
Chronic liver disease may boost risk of colorectal cancer
Last Updated: 2017-01-18
By Lorraine L. Janeczko
NEW YORK (Reuters Health) - Patients with chronic liver
disease may have an elevated risk for colorectal cancer (CRC),
even after a liver transplant, according to a systematic review
and meta-analysis.
"Patients with chronic liver disease, regardless of the
cause, had an increased risk of colorectal cancer that persisted
after liver transplant," senior author Dr. Atsushi Sakuraba of
the University of Chicago Medicine in Illinois told Reuters
Health.
"A more intensive screening/surveillance colonoscopy program
to reduce mortality from colorectal cancer should be applied to
patients with chronic liver disease," he advised in an email.
Dr. Sakuraba and his colleagues assessed the risk of CRC in
patients with chronic liver diseases before and after liver
transplantation. They searched electronic databases for studies
assessing the risk of CRC in patients with chronic liver
diseases and identified 55,991 patients in 50 studies.
In a paper online December 21 in Gastrointestinal Endoscopy,
they report that among studies that included patients with
hepatitis and cirrhosis, the pooled standardized incidence rate
(SIR) was 2.06 (P<0.0001; 95% confidence interval 1.46 to 2.90)
with moderate heterogeneity (I-squared statistic=49.2%), likely
due to the difference between the disease subgroup and the power
of the studies.
Three studies showed an increased risk of CRC in primary
sclerosing cholangitis (PSC) (pooled SIR 6.70; P<0.0001; 95% CI,
3.48 to 12.91) with moderate heterogeneity (I2=36.3%),
apparently due to the difference between the power of the
studies.
Of the studies that included post-transplant patients, the
pooled SIR was 2.16 (P<0.0001; 95% CI, 1.59 to 2.94) with
moderate heterogeneity (I2=56.4%).
On meta-regression, a correlation was found between the
proportion of autoimmune-related liver diseases and the risk of
CRC.
"It was previously thought that only patients with PSC had
an increased risk of colorectal cancer, but our study showed
that patients with other liver diseases also have an increased
risk," Dr. Sakuraba said.
"It would be important to study" whether patients with other
chronic liver diseases "are equally at increased risk," Dr.
Sakuraba explained.
Dr. Patrick Boland of the Roswell Park Cancer Institute in
Buffalo, New York, who was not involved in the study, noted in
an email that "most patients here had cirrhosis, PSC or a prior
liver transplant. The most convincing increased risk was seen in
patients who had PSC, which is associated with inflammatory
bowel disease, a known risk factor for colon cancer."
"However," he said, "the post-transplant patients, and
specifically those patients with underlying autoimmune diseases,
also had increased risk of colon cancer."
"Organ transplantation requires the use of immune
suppressive drugs, with a long-term risk of secondary
malignancies," he noted. "We already have evidence that patients
with a prior kidney transplant have an increased risk of colon
cancer. These data would suggest that patients who are being
evaluated for and/or who have undergone a liver transplantation
are at approximately a two-fold greater risk for developing
colon cancer."
Dr. Boland said the findings are not entirely surprising
because links to inflammation, immune suppression, and the risk
of colon cancer are known.
"One might consider colonoscopy as part of the liver
transplant workup, particularly in patients with primary
sclerosing cholangitis (PSC)," he suggested.
"It would be very interesting to know if this risk is
predominantly linked to an increase in right-sided vs left-sided
colon cancers, knowing that there are important biologic
differences between cancers arising in different portions of the
large bowel," Dr. Boland said.
The Pediatric Oncology Research Fellowship of the Children's
Cancer Association of Japan helped fund the study.
SOURCE: http://bit.ly/2iRQeR9
Gastrointestinal Endosc 2016.
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