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  1. Jan 1, 2018 · Prof Gerhardt Attard MD PhD FRCPProf Attard is a John Black Charitable Foundation Endowed Chair in Urological Cancer Research at University College London. He holds an advanced Cancer Research UK Clinician Scientist award and is Team Leader of the Treatment Resistance Group at the UCL Cancer Institute. He graduated with a degree in Medicine ...

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      Prof Gerhardt Attard MD PhD FRCPProf Attard is a John Black...

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      Co-authors Attard G, Murphy L, Clarke NW...97 more. PDF...

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  2. Sep 26, 2021 · This subsection of the study was led by Gerhardt Attard, MD, PhD, John Black Charitable Foundation endowed chair in urological cancer research at University College London. He now believes the findings should be used as a new ‘Standard of Care’.

  3. Prof Attard is a John Black Charitable Foundation Endowed Chair in Urological Cancer Research at University College London. He holds an advanced Cancer Research UK Clinician Scientist award and is Team Leader of the Treatment Resistance Group at the UCL Cancer Institute.

  4. Sep 23, 2021 · Study author Gerhardt Attard, MD, PhD, John Black Charitable Foundation Endowed Chair in Urological Cancer Research at University College London, said, “Based on these results, all men with high-risk nonmetastatic prostate cancer should be considered for 2 years of abiraterone.

  5. Prof Attard is a John Black Charitable Foundation Endowed Chair in Urological Cancer Research at University College London. He holds an advanced Cancer Research UK Clinician Scientist award and is Team Leader of the Treatment Resistance Group at the UCL Cancer Institute.

  6. Jan 29, 2022 · Abiraterone acetate and prednisolone with or without enzalutamide for high-risk non-metastatic prostate cancer: a meta-analysis of primary results from two randomised controlled phase 3 trials of the STAMPEDE platform protocol.

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  8. Dr. Attard ended by summarizing that two years of AAP-based therapy significantly improved MFS and OS in men with high-risk M0 prostate cancer starting ADT. Adding ENZ to AAP increased toxicity with no discernible impact on efficacy.

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