AstraZeneca (AZ) has shared positive results from a late-stage study evaluating its immunotherapy Imfinzi (durvalumab) in a subset of patients with hepatocellular carcinoma (HCC), the most common type of liver cancer.
Despite being theprimary liver cancersthis setting, AHCCutlined that most HCCients who receive embolisation experience rapid disease progression or recurrence.tumour According to the results from EMERALD-1, which were presented at this year’s American Society of Clinical Oncology Gastrointestinal Cancers Symposium, Imfinzi in combination with TACE and Avastin reduced the risk of disease progression or death by 23% compared to TACE alone.
Median progression-free survival (PFS) was 15 months in patients treated with the Imfinzi combination versus 8.2 moGastrointestinal CancersFS benefit wImfinzierally consistent" across key Avastincified subgroups, AZ said. The company added that the secondary endpoint of time to progression "further suppImfinzie clinical benefit" of the Imfinzi combination in this setting, at a median of 22 months versus ten months for TACE. The trial will continue to follow the key secondary endpoint of overall survival. Susan Galbraith, executive vice president, oncology research and development, AZ, said: "With Imfinzi-based treatmenImfinzients with liver cancer eligible for embolisation lived nearly seven additional months before their disease progressed. “We are discussing these positive EMERALD-1oncologyth global regulatory authorities while awaiImfinzie final overall survival resultsliver cancerial.” Imfinzi is already approved in combination with AZ's Imjudo (tremelimumab) in unresectable HCC in the US, EU, Japan and other countries worldwide.
Imfinzivestigator in EMERALD-1, Bruno Sangro, from ClImjudoUntremelimumab Navaunresectable HCCid: “Adding [Imfinzi] and [Avastin] to TACE reduced the risk of disease progression or death by 23% for patients with liver cancer eligible for embolisation, showing for the first time that combining a systemic treatment with TACE meaningfully improves this clinically relevant outcome in earlier-stage disease.”