The FDA's Oncologic Drugs Advisory Committee (ODAC) unanimously
recommended accelerated approval for bevacizumab (Avastin) for the
treatment of glioblastoma multiforme (GBM), an aggressive and nearly
uniformly fatal form of brain cancer. The drug's manufacturer,
Genentech, is seeking an indication for bevacizumab as monotherapy for
previously treated GBM patients. The panel’s vote of 10-0 for approval
was based on results of two phase 2 studies of bevacizumab in GBM.
In one of the studies involving 167 patients with treatment-refractory
GBM, bevacizumab monotherapy (10 mg/kg every two weeks) resulted in a
partial response rate of 26%, with median a median response duration of
4.2 months. No patients in the study had a complete response. The
6-month progression free-survival rate was 36%, and one-year overall
survival was about 38%. Historically, among patients with progressive
GBM who receive salvage chemotherapy, on average only about 25% remain
alive at one year.
The other study, which involved
56 patients with previously treated high-grade gliomas, produced an
objective response rate of 20% and a median duration of response of 3.9
months.
Treatment response in GBM is difficult to assess because the disease
disrupts the blood-brain barrier, which often creates significant brain
edema. This shows up as increased contrast enhancement on MRI.
Bevacizumab reduces the leakiness of blood vessels surrounding the
tumor, and consequently improves contrast enhancement. It is unclear,
however, to what extent this effect may represent a true anti-tumor
response, a concern cited by the FDA panel. There is some evidence that
GBM may continue to progress even in the presence of reduced edema.
Nonetheless, the advisory panel found the trial results compelling
enough to unanimously recommend approval.
The FDA is not obligated to follow advisory committee recommendations,
but usually does so. A final agency decision is expected by early May.
By
Roderick Smith, M.S.
References: http://www.gene.com/gene/news/pressreleases/display.do?method=detail&id=12027