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Brivanib fails to match sorafenib for liver cancer, but tivantinib looks promising
Liz Highleyman, 2012-12-05 09:10:00
The investigational cancer drug brivanib did not significantly increase survival for people with hepatocellular carcinoma over existing standard therapy, researchers reported at the recent Liver Meeting 2012, the 63rd Annual Meeting of the American Association for the Study of Liver Diseases (AASLD) in Boston. But another drug, tivantinib, did appear beneficial for a subset of patients.
Over years or decades chronic hepatitis B or C, heavy alcohol consumption or other causes can lead to severe liver disease including cirrhosis and hepatocellular carcinoma (HCC), a form of primary liver cancer. One of the most common cancers worldwide – especially in Asia – it is often not detected until advanced stages and is therefore difficult to treat.
The multikinase inhibitor sorafenib (Nexavar) is currently the only drug shown to extend survival for liver cancer patients who are not eligible for resection or surgical removal. Like many cancer drugs, however, it can be difficult to tolerate.
Philip Johnson, from the University of Birmingham, and an international team of colleagues conducted the phase 3 BRISK-FL trial to evaluate the safety and efficacy of sorafenib versus brivanib, a selective inhibitor of receptors for vascular endothelial growth factor and fibroblast growth factor, two chemical messengers that play a role in liver cancer development. In previous trials brivanib demonstrated anti-tumour activity, though it did not extend overall survival compared with placebo.
BRISK-FL enrolled 1155 people with advanced HCC who had received no prior systemic treatment. Most (84%) were men, about two-thirds were Asian and the median age was 60 years. About 45% had hepatitis B, about 20% had hepatitis C and about 15% had alcoholic liver disease. More than 90% were Child-Pugh stage A. Half had distant metastasis, or spread beyond the liver, and just over one-quarter had regional lymph node metastasis.
Participants were randomly assigned to receive 800mg oral brivanib or 400mg oral sorafenib, both twice daily. They were followed until they experienced disease progression or unacceptable toxicity. The researchers looked at overall survival as a primary endpoint, as well as time to progression, objective response rate, disease control rate and quality of life.
The median duration of treatment was 3.2 months in the brivanib arm and 4.1 months in the sorafenib arm. Median overall survival was 9.5 months in the brivanib arm compared with 9.9 months in the sorafenib arm, not a statistically significant difference. No significant survival differences were seen in subgroups based on geographic region, cause of HCC or disease severity.
The median time to progression was 4.2 months in the brivanib arm compared with 4.1 months in the sorafenib arm, again not a significant difference. Less than 1% of people in the both treatment groups experienced complete response. Partial response was seen in 12% of patients in the brivanib arm and 8% in the sorafenib arm. About half of participants in both arms (54 vs 56%, respectively) had stable disease, whilst disease progression occurred in 16 and 24%, respectively.
Objective response rates as reported by patients were 12% in the brivanib arm and 9% in the sorafenib arm, a difference that fell just short of statistical significance; 46% of brivanib recipients and 53% of sorafenib recipients discontinued the study early due to disease progression.
Both brivanib and sorafenib were difficult to tolerate, with more that half of patients in both arms experiencing serious adverse events (59 vs 52%, respectively. Rates of adverse events leading to treatment discontinuation were 43 and 33%, respectively. Most deaths during the study were due to cancer progression; 1.6 vs 0.3%, respectively, in the two treatment arms were attributed to drug toxicity.
Loss of appetite, fatigue, nausea, vomiting, high blood pressure and low blood sodium were at least 10% more common in the brivanib arm, whilst hair loss, rash and hand or foot skin reactions were more common in the sorafenib arm. Patients' quality of life declined considerably in both arms by week 12 of treatment, slightly but significantly more so in the brivanib arm.
Based on these findings the researchers concluded: "The primary endpoint of non-inferiority in overall survival for brivanib vs sorafenib was not met." However, they added, "Brivanib had antitumour activity similar to sorafenib", based on time to progression, objective response rate and disease control rate. "Brivanib had an acceptable safety profile" but was "generally less well-tolerated than sorafenib".
At a conference overview for the media, AASLD president Guadalupe Garcia-Tsao said that, since brivanib showed no improvement in survival over sorafenib but was less well-tolerated, "sorafenib will continue to be the standard of care for these patients".
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