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Enrique Trilla

Researcher at University of Barcelona

Publications -  56
Citations -  935

Enrique Trilla is an academic researcher from University of Barcelona. The author has contributed to research in topics: Medicine & Prostate cancer. The author has an hindex of 12, co-authored 25 publications receiving 808 citations.

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Redefining clinically significant castration levels in patients with prostate cancer receiving continuous androgen deprivation therapy.

TL;DR: The lowest testosterone castration level with clinical relevance in medically castrated patients with prostate cancer was 32 ng/dl, and maximal androgen blockade provided a significantly longer survival free of androgen independent progression in those with breakthrough increases greater than 50 ng/DL.
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Prevalence of osteoporosis during long-term androgen deprivation therapy in patients with prostate cancer.

TL;DR: The prevalence of osteoporosis seemed high in hormone-naive patients with prostate cancer, and it increased to more than 80% after 10 years ofADT, and clinicians should be aware of the impact of ADT on BMD to prevent bone mass loss.
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Bone Mineral Density Changes in Patients With Prostate Cancer During the First 2 Years of Androgen Suppression

TL;DR: Bone mineral density decreases during the first 24 months of androgen suppression with the most relevant effect occurring in the first year.
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Failure to maintain a suppressed level of serum testosterone during long-acting depot luteinizing hormone-releasing hormone agonist therapy in patients with advanced prostate cancer.

TL;DR: A small but clinically significant rate of patients under 3-month luteinizing hormone-releasing hormone agonist therapy fail to achieve or maintain castrate testosterone serum levels, which supports the need of monitoring testicular response during LH-RH agonists therapy.
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Nadir prostate-specific antigen best predicts the progression to androgen-independent prostate cancer.

TL;DR: Results show that the ability to achieve an undetectable nadir PSA and the time to reach it are the most significant predictors of the time of AIP in patients with locally advanced and metastatic prostate cancer under androgen suppression as a single therapy.