PFS was the primary endpoint of the DCVax-L trial. naive OS was the secondary endpoint. From the original protocol posted on clinicaltrials.gov:
Primary Outcome Measures: 1. The primary objective of this study is to compare progression free survival from time of randomization between patients treated with DCVax-L and control patients. [ Time Frame: Time to tumor progression or death ]
Secondary Outcome Measures: 1. The secondary objective is to compare overall survival and time to disease progression between DCVax-L treated and control patients. [ Time Frame: Until Death ]
Bottomline, PFS and OS are both "REAL" data results.