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L. Michael Glode

Researcher at University of Colorado Denver

Publications -  70
Citations -  3711

L. Michael Glode is an academic researcher from University of Colorado Denver. The author has contributed to research in topics: Prostate cancer & Cancer. The author has an hindex of 27, co-authored 69 publications receiving 3478 citations. Previous affiliations of L. Michael Glode include University of Colorado Boulder & Anschutz Medical Campus.

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Overall Survival Analysis of a Phase II Randomized Controlled Trial of a Poxviral-Based PSA-Targeted Immunotherapy in Metastatic Castration-Resistant Prostate Cancer

TL;DR: PROSTVAC-VF immunotherapy was well tolerated and associated with a 44% reduction in the death rate and an 8.5-month improvement in median OS in men with mCRPC, providing preliminary evidence of clinically meaningful benefit but need to be confirmed in a larger phase III study.
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A phase I and pharmacokinetic study of silybin-phytosome in prostate cancer patients.

TL;DR: It is concluded that 13 g of oral silybin-phytosome daily, in 3 divided doses, appears to be well tolerated in patients with advanced prostate cancer and is the recommended phase II dose.
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Lipid Catabolism via CPT1 as a Therapeutic Target for Prostate Cancer

TL;DR: Systemic treatment with etomoxir in nude mice resulted in decreased xenograft growth over 21 days, underscoring the therapeutic potential of blocking lipid catabolism to decrease prostate cancer tumor growth.
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The use of trastuzumab in the treatment of hormone refractory prostate cancer; phase II trial†

TL;DR: To investigate the efficacy and toxicity of the antibody to the HER‐2/neu receptor (trastuzumab, Herceptin®) in the treatment of advanced hormone‐refractory prostate cancer (HRPC).
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Metronomic therapy with cyclophosphamide and dexamethasone for prostate carcinoma

TL;DR: The current study was designed to evaluate the efficacy and toxicity of the continuous oral administration of a combination of cyclophosphamide and dexamethasone in patients with prostate specific antigen (PSA) progression despite single or multiagent hormone therapy and antiandrogen withdrawal.