
EDITORIAL

This is the third
consecutive issue of HTB to lead with an FDA or EMEA drug warning letter.
The issue this month
is that the triple-nucleoside combination of ddI/3TC/tenofovir failed
to produce a viral load reduction >2logs by week 12 in a group of treatment
naïve patients. It did however provide nearly all of them with their
first set of drug-resistant mutations. It should be noted that the European
version of this issue letter from Gilead also cautions against using ddI/3TC/tenofovir
in treatment experienced patients.
Fortunately, this
combination is unlikely to be currently widely used in the UK, and the
caution against triple-nucleoside combinations in the 2003 BHIVA guidelines
should limit any further prescribing of any triple-nucleoside combination
in first-line therapy.
A further report of
yet another poorly performing triple-nucleoside combination - this time
with abacavir/ddI/d4T - is included on page 16.
The November HTB issue
also includes a report on strategic treatment interruptions studies in
resource-limited settings from the 13th International Conference on AIDS
and STIs in Africa (ICASA).
STIs have now been
well studied in countries which have widespread access to ARV therapy,
and results from recent studies are reported on page 18-19.
These finding have
not been particularly encouraging and the risk from resistance when stopping
and restarting NNRTI-based regimes will apply wherever these studies are
being run.
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