Avastin Shows Promise As Aggressive Brain Cancer Drug
Featured ArticleMain Category: Cancer / Oncology
Also Included In: Neurology / Neuroscience; Clinical Trials / Drug Trials; Regulatory Affairs / Drug Approvals
Article Date: 19 Nov 2007 - 7:00 PDT
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Phase II trials of Avastin (bevacizumab) for the treatment of aggressive brain cancer have shown promising results, said Genentech, makers of the drug, who presented their findings at the 12th Annual Scientific Meeting of the Society for Neuro-Oncology that took place between 15th and 18th November, in Dallas, Texas.
Avastin (bevacizumab) is a monoclonal antibody that inhibits the growth of tumours by blocking the production of new blood vessels (angiogenesis) that would feed the tumour. The drug, which has been described as a "blockbuster" cancer drug, was one of the first clinically available angiogenesis inhibitors in the US.
Given alone or with irinotecan chemotherapy in a randomized, multi-center, phase II trial, the drug showed an encouraging six-month progression-free survival (PFS) and objective response rate in patients with the most common and aggressive type of brain cancer, relapsed glioblastoma multiforme (GBM).
According to the American Cancer Society (ACS), only 3 per cent of patients with GBM survive longer than 5 years, and this figure has not altered in 25 years. The Society estimates that in 2007 there will be 20,500 new cases of brain cancer and 12,740 brain cancer deaths in the US.
36 per cent (31 out of 85) patients treated with Avastin alone, and 51 per cent (42 out of 82) treated with Avastin combined with chemotherapy, lived without the disease advancing within six months, reported Genentech, who said the results were "assessed by independent radiological review".
Genentech researchers said they observed no new or unexpected safety events related to Avastin.
Dr Timothy Cloughesy, lead researcher of the study, and director of the Neuro-Oncology Program of the Jonsson Comprehensive Cancer Center at the University of California, Los Angeles (UCLA) said that:
"Historical estimates suggest that only 15 percent of patients with this aggressive type of brain cancer live without their cancer progressing within six months."
"The findings suggested that at six months, more patients had lived without their cancer advancing when Avastin was administered as a single-agent or in combination with chemotherapy, than what we would normally expect," he added.
In this phase II, open-label, multicenter, randomized, non-comparative study, Cloughesy and colleagues enrolled 167 patients with GBM whose cancer had relapsed. They were randomized to either an Avastin alone or Avastin with irinotecan chemotherapy group, and all patients had received prior temozolimide. The treatment was administered every other week for up to two years (104 weeks).
The main outcome measure was PFS, which was defined as the "absence of any event of cancer progression or death". The researchers also assessed overall survival and safety.
As well as the six-month PFS rates of 36 and 51 per cent in the Avastin only and Avastin with chemotherapy groups, the results also showed that:
- Preliminary estimates of tumour response were seen in 21 per cent (18 of 85) of patients treated with Avastin only.
- The figure for Avastin with chemotherapy was 34 per cent (28 out of 82).
- Adverse events linked to Avastin were similar to previous trials.
- The most common severe (grade 3 or higher) toxicities in the Avastin only group were: hypertension (8 per cent), and convulsion (6 per cent).
- The figure for the Avastin plus chemotherapy group were: convulsion (13 per cent) and neutropenia (9 per cent); neutropenia is a condition where there is a low count of neutrophils, a type of white blood cell.
- Grade 1 and grade 3 intercranial (brain) hemorrhage occurred in 2 participants in the Avastin only group.
- One patient had a grade 4 hemorrhage in the Avastin plus chemotherapy group.
- Two deaths were linked to adverse events in the Avastin only group, and one in the Avastin plus chemotherapy group.
The trial is still ongoing and final figures for safety and other efficacy results will be available in 2008, said the researchers.
Avastin was first approved by the FDA in February 2004, to treat metastatic colorectal cancer in combination with chemotherapy. Since then it has been approved for particular types of lung cancer. There are currently over 300 trials worldwide assessing the drug's potential to treat over 20 different types of tumour.
Click here for FDA information on Avastin (bevacizumab).
Written by: Catharine Paddock
Copyright: Medical News Today
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Avastin Shows Promise As Aggressive Brain Cancer Drug
posted by Gregory D. Pawelski on 25 Nov 2007 at 1:41 pmResearch has shown that controlling production of new blood vessels can restrict tumor growth, often prolonging the life of the cancer patient. Perhaps the most widely-used anti-angiogenic agent to emerge to date has been the drug Avastin.
Avastin has shown activity in many solid tumor types. As with most "targeted" therapy drugs, Avastin does not necessarily benefit every patient and it is expensive. Until now, there were no tests that existed to show reliably who would benefit from anti-angiogenic agents.
There has been an bio-marker assay (AngioRx™) developed for microvascular viability to identify potential responders to Avastin, Nexavar, Sutent, and other anti-angiogenic drugs. It was discovered that endothelial cells are present in tumor microclusters and it appears that drug effect upon these cells can be assessed in the new microvascular viability assay.
The assay has a morphological endpoint which allows for visualization of both tumor and microvascular cells and direct assessment of both anti-tumor and anti-microvascular drug effect. CD31 cytoplasmic staining confirms morphological identification of microcapillary cells in a tumor microcluster.
The principles and methods used in the assay include: 1. Obtaining a tissue, blood, bone marrow or malignant fluid specimen from the patient. 2. Exposing viable tumor cells to anti-neoplastic drugs. 3. Measuring absolute in vitro drug effect. 4. Finding a statistical comparison of in vitro drug effect to an index standard, yielding an individualized pattern of relative drug activity. 5. Information obtained is used to aid in selecting from among otherwise qualified candidate drugs.
Confirmatory activities are ongoing. It is being offered currently to selected clients on a research basis and as an adjunct to a standard assay or a tyrosine kinase assay.
http://weisenthalcancer.com/Patient%20Pages/AngioRx.htm
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