Wellstat Biologics (United States)

IntroductionThe elevation of aminotransferase levels is regarded as an indicator of hepatocellular injury. The objective of this study was to describe real-world incidence of elevated aminotransferase levels with or without bilirubin elevation among patients treated with immune checkpoint inhibitors (ICIs) for solid tumors.MethodsThis retrospective cohort study used an electronic health record database representing > 1.5 million active United States (US) cancer patients and included patients diagnosed with any cancer between January 1, 2014 and March 31, 2019, and treated with one or more ICIs such as ipilimumab, tremelimumab, nivolumab, pembrolizumab, atezolizumab, durvalumab, and avelumab. The frequency, onset, duration, management of grade ≥ 3 elevation of aminotransferase levels with or without bilirubin elevation events, progression rate from isolated elevation of aminotransferase levels (IAT) to elevated aminotransferase levels with elevated bilirubin (ATWB), and mortality were described.ResultsOverall, 69,140 patients received 85,433 treatment courses. A total of 1,799 (2.11%) IAT and 441 (0.52%) ATWB events were observed during treatment courses. The median onset was 51 and 42 days for IAT and ATWB, respectively, across treatment courses, and the median duration of both was approximately seven days. Approximately 5% (n=96) of IAT events progressed to ATWB in a median time of 11 days. The proportion of patients who received corticosteroids after elevated aminotransferase levels with or without bilirubin was ~37% (n=671/1,799 of IAT and n=147/441 of ATWB) and ~8% discontinued ICI treatment (n=118/1,799 of IAT and n=43/441 of ATWB). About 46% (n=68/147) of ATWB and and 25% (n=172/671) of IAT events treated with steroids led to death within 45 days. Similarly, 49% (n=21/43) of ATWB and 35% (n=42/118) of IAT events leading to treatment discontinuation led to death within 45 days.ConclusionsReal-world data from oncology clinics in US suggest low incidence of grade ≥ 3 elevated aminotransferase levels with or without bilirubin elevation following treatment with ICIs. In most cases, ICI treatment was not discontinued and management of elevated aminotransferases consisted of corticosteroid treatment in one-third of cases.

PV701 is a highly purified, replication-competent naturally attenuated strain of Newcastle disease virus, an avian paramyxovirus. PV701 directly lyses diverse human cancer cells in vitro (oncolytic) while being significantly less toxic toward normal human cells. In addition to its direct oncolytic properties, PV701 is capable of stimulating T-cell-mediated specific antitumor immunity and nonspecific activation of immune function, including interferon release and activation of tumoricidal macrophages. A high rate of complete tumor regression is observed in athymic mice implanted with human tumor cells following PV701 administered intravenously, or by intraperitonel or intratumoral routes. Objective responses have been observed in human phase I clinical trials of diverse tumor types. PV701 thus warrants further study as a novel therapeutic agent for cancer patients.Key WordsOncolyticPV701Newcastle disease virustumoricidalparamyxovirus