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Updated: Dec 14, 2025

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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The evolving options in metastatic castration-sensitive prostate cancer
1Centre Hospitalier de l'Université de Montréal, Montréal, Canada.
Current Opinion in Supportive and Palliative Care
|July 24, 2020
Summary
New treatments for metastatic castration-sensitive prostate cancer (mCSPC) offer survival benefits. Androgen deprivation therapy (ADT) combined with novel agents like enzalutamide and apalutamide, alongside docetaxel and abiraterone acetate, are key advancements.
Area of Science:
- Oncology
- Urology
- Medical Treatments
Background:
- Metastatic castration-sensitive prostate cancer (mCSPC) treatment has evolved significantly.
- Established guidelines include androgen deprivation therapy (ADT) with docetaxel or abiraterone acetate, based on trials like CHAARTED and LATITUDE.
Purpose of the Study:
- To review recent advancements in mCSPC treatment.
- To compare novel therapeutic combinations and emerging evidence.
- To guide personalized treatment strategies for mCSPC patients.
Main Methods:
- Review of randomized controlled trials investigating new treatment combinations for mCSPC.
- Analysis of data from trials involving enzalutamide and apalutamide with ADT.
- Evaluation of emerging evidence for radiotherapy in metastatic prostate cancer.
Main Results:
- Recent trials demonstrate survival gains with enzalutamide plus ADT and apalutamide plus ADT in mCSPC.
- These combinations expand therapeutic options beyond established treatments.
- Emerging data suggests potential benefits of radiotherapy for the primary tumor in metastatic settings.
Conclusions:
- Novel androgen receptor inhibitors (enzalutamide, apalutamide) combined with ADT represent significant progress in mCSPC management.
- Distinguishing between these therapies is crucial for personalized patient care.
- Further research into radiotherapy's role may offer additional treatment avenues.
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