Presented are the efforts of the Pharmaceutical Research and Manufacturing Association PFS Working Group to address concerns related to blinded independent central review of locally evaluated progression times and the proposed audit methodology to minimize potential biases, along with the U.S. Food and Drug Administration's comments on this work.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227978PMC
http://dx.doi.org/10.1634/theoncologist.2009-0261DOI Listing

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