CHRONIC HEPATITIS-C LONG-TERM RESPONDERS TO HUMAN-LEUKOCYTE INTERFERON-ALPHA THERAPY - PERSISTENCE OF A SUSTAINED BIOCHEMICAL AND VIROLOGICAL RESPONSE DURING 5 YEARS OF SURVEILLANCE
F. Morisco et al., CHRONIC HEPATITIS-C LONG-TERM RESPONDERS TO HUMAN-LEUKOCYTE INTERFERON-ALPHA THERAPY - PERSISTENCE OF A SUSTAINED BIOCHEMICAL AND VIROLOGICAL RESPONSE DURING 5 YEARS OF SURVEILLANCE, European journal of gastroenterology & hepatology, 10(5), 1998, pp. 399-403
Objectives To define the biochemical and virological course and IgM re
sponse to HCV-core protein in longterm responders (LTRs) during a long
surveillance (5 years). Design From 1989 to 1991, 98 patients (pts) w
ith biopsy-proven chronic hepatitis C were enrolled into this study. T
hese pts underwent human leukocyte interferon-alpha (LE-IFN alpha) the
rapy at the prolonged schedule (3 MU thrice weekly for 1 year), Method
s Serum alanine-aminotransferases (ALTs) were assessed monthly during
and until 1 year after treatment, then every 3 months during the obser
vation period. Qualitative and quantitative HCV RNA and HCV IgM were m
easured in all pts on baseline samples and in LTRs also after treatmen
t and every following year, Results Based on serum ALT course, the pts
were defined as: LTRs (14 pts), if their serum ALT levels returned to
the normal range during therapy and remained so for at least 1 year a
fterwards; responders with relapse (RRs, 20 pts), if their serum ALT l
evels returned to the normal range during therapy but increased after
ending treatment; and non-responders (NRs, 64 pts), if their serum ALT
levels remained abnormal throughout therapy. No significant differenc
es were seen regarding IgM anti-HCV positivity and serum ALT levels am
ong the three groups, LTRs (12 HCV-RNA negative and two HCV-RNA positi
ve at the end of treatment) maintained their virological status and no
t one of them experienced an elevation of serum ALT levels throughout
the surveillance. Conclusion Patients affected by chronic hepatitis C
and treated with interferon, but who did not experience a biochemical
or virological relapse within the first year of follow-up would not re
lapse later on; thus, we are able to conclude that these subjects made
a complete recovery. (C) 1998 Lippincott-Raven Publishers.