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Updated: Jan 15, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Treatment Trajectories in Metastatic Hormone-sensitive Prostate Cancer: A PIONEER+ Big Data Analysis
Rossella Nicoletti1, Alex Qinyang Liu2, Susan Evans-Axelsson3
1Department of Experimental and Clinical Biomedical Science, University of Florence, Florence, Italy; Unit of Urology and Renal Transplantation, Careggi University Hospital, Florence, Italy; SH Ho Urology Centre, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, Hong Kong.
Real-world data show androgen deprivation therapy plus an androgen receptor pathway inhibitor improves metastatic hormone-sensitive prostate cancer outcomes. Despite this, androgen deprivation therapy monotherapy remains common, suggesting a need for broader adoption of combination therapies.
Area of Science:
- Oncology
- Real-world evidence
- Prostate cancer research
Background:
- Metastatic hormone-sensitive prostate cancer (mHSPC) treatment is rapidly evolving.
- Real-world data (RWD) are crucial for understanding actual treatment patterns and outcomes.
- The PIONEER project leverages large-scale RWD to analyze mHSPC treatment trajectories.
Purpose of the Study:
- To describe treatment patterns and clinical outcomes in a large, multicenter mHSPC cohort using RWD.
- To analyze treatment switch, progression, adverse events, and survival in mHSPC patients.
- To evaluate the real-world effectiveness of different mHSPC treatment strategies.
Main Methods:
- Utilized eight European and US databases (2016-2020) standardized to the Observational Medical Outcome Partnership Common Data Model.
- Identified patients diagnosed with mHSPC and those receiving treatment.
- Analyzed outcomes including treatment switch, symptomatic progression, adverse events, and death.
Main Results:
- Over 107,000 mHSPC patients identified; 67,909 received treatment.
- Androgen deprivation therapy (ADT) monotherapy was most common (69.4%), followed by ADT + androgen receptor pathway inhibitor (ARPI; 15.2%).
- ADT + ARPI demonstrated higher persistence (53.8%) and improved 5-year switch-free survival (up to 72.3%) compared to ADT monotherapy.
Conclusions:
- This is the largest RWD study on systemic mHSPC treatment.
- ADT monotherapy remains the most frequent first-line therapy despite evidence supporting other options.
- Increased use of ADT + ARPI is linked to better persistence and outcomes, supporting its wider clinical adoption.
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