High levels of bilirubin at baseline and low
albumin levels were risk factors for the development of liver
decompensation and/or serious adverse events among patients with
hepatitis C virus infection treated with Sovaldi-based regimens.
of new HCV treatments in real-world clinical practice, Ponni V. Perumalswami, MD,
assistant professor of medicine, division of liver diseases, Icahn
School of Medicine at Mount Sinai, New York, and colleagues evaluated
data of 511 patients with HCV
who initiated treatment with Sovaldi- (sofosbuvir, Gilead Sciences)
based regimens at Mount Sinai Medical Center between December 2013 and
June 2014. The researchers assessed the data by two methods: clinicians
created lists of all patients who began treatment and experienced
hepatic decompensation or a serious adverse event
within 1-month post-treatment, and patients on treatment were queried
from the Mount Sinai Data Warehouse medical records database.
Of the 511 patients, 499 had no history of
hepatic decompensation during the previous 12 months, therefore were
included in a nested case–control study to identify predictors of
decompensation and/or serious adverse events. Cases and controls were
matched 1:5 based on treatment regimen and duration.
Overall, the cumulative incidence of
decompensation and/or serious adverse events was 6.4% for the entire
cohort. Among the 499 previously stable patients, the incidence of
decompensation and/or serious adverse events was 4.5%, with a mortality
rate of 0.6%.
Of the 499 patients, 16 experienced one or
more serious adverse events that were deemed potentially
treatment-related. The sustained virological response rate was 44% for
these patients (7/16).
Two of the 16 cases had complications
consistent with autoimmune events and one experienced a flare of
autoimmune hepatitis. Both underwent treatment with sofosbuvir and
Olysio (simeprevir, Janssen). Compared with controls, the 16 cases had higher baseline median MELD scores (14 vs. 8; P <
.01). Decompensation and/or serious adverse events were independently
associated with lower baseline albumin and higher total bilirubin (P = .01 for both).
The researchers concluded: “Among HCV
mono-infected patients, decreased hepatic reserve appears to be a risk
factor for decompensation and [serious adverse events] on HCV treatment
with [sofosbuvir]-containing regimens. These patients may benefit from
more intensive monitoring during and for several months after
discontinuing treatment.” – by Melinda Stevens
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