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I am working with a global patient outcome organization seeking to know how much authority prostate cancer patients in France have in asking for tests or for specific treatments. We want to help increase patient involvement in decision making with their physicians. Are there areas for improvement? Does access to care depend upon reimbursement for tests and treatments? Thanks for your answers in advance! Merel
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I have copied this post to the Prostate section of the "Specific cancers Forum" where it may get more exposure. Could you tell us more about this study, please?