Progressive multifocal
leukoencephalopathy (PML)
June 2007 View PDF En
español
Potent anti-HIV therapy
Several groups have reported symptom-free survival after a PML
diagnosis of over ten years and counting for some people using potent
anti-HIV therapy. Factors associated with improved survival include
using an anti-HIV regimen with a protease inhibitor and changing
to a new regimen after a PML diagnosis.
A more recent study shows extremely encouraging results, perhaps
the best to date, with “enhanced” anti-HIV therapy.
This is when Fuzeon (enfuvirtide, T-20) is added to a traditional
regimen with protease inhibitors. At six months, the survival rate
was 3 out of 4 people and the trend suggested this survival rate
may hold to one year and beyond.
While there are no guidelines for anti-HIV therapy and PML, it
would be fair to make a few assumptions based on gathered information.
After a presumptive diagnosis of PML is made and whether or not
a person elects to have a brain biopsy, it seems advisable to start
or change to a new potent anti-HIV regimen including a protease
inhibitor. Experienced neurologists who choose to treat PML with
anti-HIV drugs once recommended using anti-HIV drugs that penetrate
the blood-brain barrier. This included using high doses of AZT daily
(1,000–1,200mg) because lower doses are not as effective at
crossing this barrier. More recently, however, experts have changed
their thinking about the importance of using drugs that cross the
blood-brain barrier in a potent anti-HIV regimen when treating PML.
Increasingly they believe that the benefits of anti-HIV therapy
are due to better immune responses throughout the body. This supports
the notion of creating the most potent possible regimen based on
resistance testing, history of anti-HIV drug use, and cross resistance
issues. This is supported by the very encouraging results of the
“enhanced” therapy study—where adding Fuzeon appears
to have a profoundly beneficial effect, but is not believed to cross
the blood-brain barrier whatsoever.
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