Condition: Prostate Cancer · Sponsor: German Oncology Center, Cyprus
The aim of this prospective, single-arm phase II study is the individualization of both radiotherapy (RT) and androgen deprivation therapy (ADT) duration for patients with high-risk localized prostate cancer (PCa) according to the National Comprehensive Cancer Network (NCCN) based on multimodal artificial intelligence (MMAI) classification. All patients will receive (i) a dose escalation to the prostate via HDR brachytherapy (boost), (ii) twelve months of ADT and (iii) extremely hypofractionated RT to the prostate (5 fractions). This way, patients in the HypoPro trial will receive a prostate-only dose escalation and benefit from shortening of the ADT compared with current guideline recommendations.
This description comes directly from the study's public registry record.
Elena Pallari, PhD · +357 25028690 · elena.pallari@goc.com.cy
Kristis Vevis, PhD · +357 25208159 · kristis.vevis@goc.com.cy
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| German Oncology Center | Limassol, Cyprus | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06772441