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U.Sregulators have approved a combination of Roche's PD-L1 monosero-tecentriq (atezolizumab) and anti-angiotherite-based monoserotrophilia monovastin (bevacionzumab) to treat unable to remove or metastatic hepatocellular carcinoma (HCC) without systemic treatmentthe approval, which makes Tecentriq in conjunction with Avastin the first and only FDA-approved cancer immunotherapy for cancer that cannot be removed or metastaticapproved the results of the Phase III IMbrave150 study, which showed that the combination of Tecentriq and Avastin reduced the risk of death by 42 percent and the risk of disease deterioration or death by 41 percent compared to Sorafini"The results of the IMbrave150 study are an important milestone in the treatment of patients with advanced liver cancer, one of the few cancers with increased mortality and limited choice of first-line treatment options
," said DrRichard Finn, a professor of medicine at the University of California, Los Angeles School of Medicine,"
" Is the first program since 2007 to improve the survival rate of sorafenib, a first-line treatment standard for hepatocellular carcinoma"