MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1080/14796694.2025.2577633

Медицинская библиотека · Future oncology (London, England) · 2025

Darolutamide plus androgen-deprivation therapy in high-risk biochemical recurrence of prostate cancer (ARASTEP).

Morgans Alicia K, Chehrazi-Raffle Alex, Niazi Tamim, Shore Neal D, Ross Ashley E, Røder Andreas, Gomes Andrea Juliana, Supiot Stephane, Barthélémy Philippe, Hatano Koji, Ruiz Carmen Belen Congregado, Yoshida Soichiro, Herrera-Imbroda Bernardo, Gratton Matthieu, Gschwend Jürgen E, Hope Thomas A, Joensuu Heikki, Kuss Iris, Le Berre Marie-Aude, Dimova-Dobreva Miryana, Fizazi Karim

СтатьяПротокол клинического исследованияПеревод в очереди

Аннотация

Patients with prostate cancer treated with radiotherapy (RT) or radical prostatectomy (RP) as primary therapy may develop biochemical recurrence (BCR), which requires effective treatment to delay disease progression. The ARASTEP study (NCT05794906) aims to determine whether the addition of darolutamide to androgen-deprivation therapy (ADT) improves radiologic progression-free survival (rPFS) using prostate-specific membrane antigen positron emission tomography/computed tomography (PSMA PET/CT) compared with placebo plus ADT in patients with high-risk BCR.Approximately 970 patients from 243 sites globally will receive either darolutamide 600 mg or placebo twice daily, both with ADT, for 24 months or until disease progression, unacceptable toxicity, or withdrawal of consent. Eligible patients will have been treated by primary RT or RP ± adjuvant RT (ART) or salvage RT (SRT), and present with high-risk BCR (prostate-specific antigen [PSA] doubling time <12 months and PSA ≥0.2 ng/mL after RP [± ART/SRT] or PSA ≥2 ng/mL above nadir after primary RT only), ≥1 PSMA PET/CT-positive lesion (negative on conventional imaging), serum testosterone >150 ng/dL, and Eastern Cooperative Oncology Group performance status 0/1. The primary endpoint is rPFS using PSMA PET/CT, with secondary endpoints including metastasis-free survival, time to castration-resistant prostate cancer, overall survival, quality of life, and safety.CLINICAL TRIAL REGISTRATION: www.clinicaltrials.gov identifier is NCT05794906.

Для цитирования: Morgans Alicia K, Chehrazi-Raffle Alex, Niazi Tamim, Shore Neal D, Ross Ashley E, Røder Andreas, Gomes Andrea Juliana, Supiot Stephane, Barthélémy Philippe, Hatano Koji, Ruiz Carmen Belen Congregado, Yoshida Soichiro, Herrera-Imbroda Bernardo, Gratton Matthieu, Gschwend Jürgen E, Hope Thomas A, Joensuu Heikki, Kuss Iris, Le Berre Marie-Aude, Dimova-Dobreva Miryana, Fizazi Karim. Darolutamide plus androgen-deprivation therapy in high-risk biochemical recurrence of prostate cancer (ARASTEP).. Future oncology (London, England). 2025. DOI: 10.1080/14796694.2025.2577633.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.