{"analyses":[{"ciLowerLimit":"0.590","ciNumSides":"TWO_SIDED","ciPctValue":"95","ciUpperLimit":"1.291","estimateComment":"The OR and confidence interval (CI) were calculated using logistic regression, adjusting for visceral metastases and cisplatin eligibility status.","groupIds":["OG000","OG002"],"nonInferiorityType":"SUPERIORITY","pValue":"0.4959","pValueComment":"P-value was based on twice the change in log-likelihood resulting from logistic regression model, adjusting for visceral metastases and cisplatin eligibility status.","paramType":"Odds Ratio (OR)","paramValue":"0.87","statisticalMethod":"Regression, Logistic"},{"ciLowerLimit":"0.305","ciNumSides":"TWO_SIDED","ciPctValue":"95","ciUpperLimit":"0.679","estimateComment":"The OR and confidence interval (CI) were calculated using logistic regression, adjusting for visceral metastases and cisplatin eligibility status.","groupIds":["OG001","OG002"],"nonInferiorityType":"SUPERIORITY","pValue":"0.0001","pValueComment":"P-value was based on twice the change in log-likelihood resulting from logistic regression model, adjusting for visceral metastases and cisplatin eligibility status.","paramType":"Odds Ratio (OR)","paramValue":"0.46","statisticalMethod":"Regression, Logistic"}],"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"49.8"},{"groupId":"OG001","value":"34.4"},{"groupId":"OG002","value":"53.1"}]}]}],"denoms":[{"counts":[{"groupId":"OG000","value":"205"},{"groupId":"OG001","value":"209"},{"groupId":"OG002","value":"207"}],"units":"Participants"}],"description":"Disease control rate (DCR) at 6 months is defined as the percentage of patients who have a best objective response (BoR) of CR or PR, or who have demonstrated SD for a minimum interval of 24 weeks (-7 days, i.e., 161 days), following the start of study treatment.","groups":[{"description":"MEDI4736 (Durvalumab) + Tremelimumab","id":"OG000","title":"Combination Therapy"},{"description":"MEDI4736 (Durvalumab)","id":"OG001","title":"Monotherapy"},{"description":"Standard of Care Chemotherapy Treatment","id":"OG002","title":"Standard of Care"}],"paramType":"NUMBER","populationDescription":"The PD-L1-High analysis set will include the subset of patients in the FAS whose PD-L1 status is PD-L1-High as defined by an Immunohistochemistry (IHC) assay developed by Ventana as:\n\n≥25% tumor cell membrane positivity for PD-L1 at any intensity above background staining as noted on the corresponding negative control OR ≥25% tumor associated immune cell positivity for PD-L1 at any intensity above background staining as noted on the corresponding negative control","reportingStatus":"POSTED","timeFrame":"Tumour scans performed at baseline then every 8 weeks since randomization until confirmed disease progression. Assessed up to 6 months or the data cut-off date (27JAN2020).","title":"Disease Control Rate (DCR) at 6 Months, PD-L1-High Analysis Set -Durvalumab + Tremelimumab Combination Therapy vs SoC and Durvalumab Monotherapy vs SoC","type":"SECONDARY","unitOfMeasure":"percentage of participants"}