These are the first results describing the real-world use of olaparib in France in prostate cancer. Most patients included in the fEA had generally similar characteristics as the patients randomized in the PROpel clinical trial (NCT03732820) and initiated at the standard dose of 300 mg twice daily. No new safety signals were reported in this real-world patient population. The analyzed data did not modify the benefit-risk balance of olaparib.
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Dourthe et al. (Mon,) studied this question.
synapsesocial.com/papers/69df2bece4eeef8a2a6b0dc2 — DOI: https://doi.org/10.1007/s40801-026-00551-z
Louis Marie Dourthe
Sorbonne Université
Aline Guillot
Université Claude Bernard Lyon 1
Cécile Vassal
Drugs - Real World Outcomes
Médipole Garonne
AstraZeneca (France)
Société du Canal de Provence
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