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747
ASPIRIN REDUCES THE INCIDENCE OF HEPATOCELLULAR
CARCINOMA IN ETVTDF TREATED PATIENTS WITH CHRONIC
HEPATITIS B
Vicki Wing-Ki Hui, Department of Medicine and Therapeutics,
Institute of Digestive Disease, the Chinese University of Hong
Kong, Hong Kong.
Background: Aspirin is known to lower the incidence rates
of cancer (e g colorectal cancer) However, the effect of
aspirin use on the risk of chronic hepatitis B (CHB)-related
hepatocellular carcinoma (HCC) in patients receiving
antiviral treatment remains undetermined This study aimed
to investigate the impact of aspirin on reducing HCC risk in
patients treated with the first-line oral nucleos(t)ide analogues
(NAs; entecavir and/or tenofovir disoproxil fumarate) We also
reported the gastrointestinal safety of aspirin use Methods:
We conducted a territory-wide, retrospective cohort study in
NA-treated CHB patients between 2000 and 2018 from the
electronic healthcare data repository in Hong Kong Subjects
were classified into aspirin users for at least 90 days during
NA treatment (i.e. aspirin group); or no aspirin or any other
antiplatelet use during follow up period (i.e. no aspirin group)
Incidence rates of HCC and gastrointestinal bleeding (GIB)
in two groups were compared with Fine-Gray subdistribution
hazard regression with propensity score weighting Results:
Of 35,516 NA-treated CHB patients of mean age 53 1 years
and 61 6% male, 1451 (67 5%) belonged to aspirin group,
whereas 20,414 (61 2%) were in no aspirin group 83 (3 9%)
and 1488 (4 5%) developed HCC at a median [interquartile
range] of 2 7[1 4-4 9] years and 3 2[1 8-6 0] years in aspirin
use group and no aspirin use group, respectively The 5-year
cumulative incidence (95% CI) of HCC were 3 3% in aspirin
use group and 3 52% in no aspirin use group (absolute risk
difference (ARD): -0.22%; 95% confidence interval [CI]:
[-0 47%, -0 03%]; p = 0 012); that of GIB were 1 59% in aspirin
use group and 0 75% in no aspirin use group (ARD: 0 84%;
95% CI: [0 7%,0 99%]; p <0 001); Aspirin reduced the risk
of HCC (adjusted subdistributional hazard ratio (sHR): 0 60;
95% CI: [0 47, 0 77] ; p <0 001) The impact of aspirin use
on GIB was undetermined (sHR: 1 32; 95% CI: [0 90,1 95]
; p = 0 157) Conclusion: Aspirin reduces the risk of HCC
in NA-treated CHB patients without a significant increase in
the risk of adverse effects such as GIB Aspirin therapy may
be a chemoprophylactic agent in such patients who are at
significant risk of HCC.
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