{"description":"Same event may appear as both non-SAE and SAE but are distinct events. An event may be categorized as serious in 1 participant and non-serious in another, or a participant may have experienced both SAE and non-SAE. For SAEs and non-SAEs safety analysis set was used. For All-cause mortality, FAS was used.","eventGroups":[{"deathsNumAffected":284,"deathsNumAtRisk":442,"description":"Participants with aRCC received avelumab 10 mg/kg, IV at Q2W in a 6-week cycle plus axitinib 5 mg, orally BID. Each treatment cycle was of 42 days.","id":"EG000","otherNumAffected":429,"otherNumAtRisk":434,"seriousNumAffected":231,"seriousNumAtRisk":434,"title":"Avelumab + Axitinib"},{"deathsNumAffected":296,"deathsNumAtRisk":444,"description":"Participants with aRCC received sunitinib 50 mg orally, QD on a schedule of 4 weeks on treatment followed by 2 weeks off treatment (schedule 4/2 in 6-week cycles). 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