APPROACH trial: Multimodal approach in patients with mHSPC: A pragmatic, randomized, phase 3 trial of androgen-deprivation therapy (ADT) plus apalutamide (APA) versus ADT plus apalutamide (APA) and local treatment—Meet-URO 29 study.

Authors

null

Valentina Guadalupi

Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

Valentina Guadalupi , Alessandro Rametta , Elena Verzoni , Melanie Claps , Pierangela Sepe , Marco Stellato , Achille Bottiglieri , Mario Catanzaro , Barbara Avuzzi , Maria Chiara Sighinolfi , Bernardo Rocco , Barbara Jereczek , Massimo Di Maio , Nicola Nicolai , Filippo G. De Braud , Giuseppe Procopio

Organizations

Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy, Department of Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy, Medical Oncology Department, Istituto Nazionale Tumori di Milano IRCCS, Milano, Italy, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy, Medical Oncology Department, Istituto Nazionale Tumori di Milano IRCCS, Milan, Italy, IRCCS Foundation National Cancer Institute, Milan, Italy, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy, Urological Department - ASST Santi Paolo e Carlo, Milan, Italy, Radiotherapy Division, European Institute of Oncology, Milan, Italy, Department of Oncology, University of Turin at Ordine Mauriziano Hospital, Torino, Italy, Torino, Italy, Urology Unit - Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy, Fondazione IRCCS Istituto Nazionale dei Tumori and University of Milan, Milan, Italy, Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

Research Funding

Pharmaceutical/Biotech Company
Janssen

Background: it is reasonable to offer radiotherapy (RT) to improve outcomes for patients with newly diagnosed M1 prostate cancer with < 5 bone metastases (HORRAD) or low volume disease (STAMPEDE) (Burdett, S et al., Eur. Urol. 2019). Data from clinical randomized trials evaluating feasibility and overall benefit of cytoreductive radical prostatectomy (cRP) in oligometastatic ormone sensitive patients are not available. The rationale for performing cytoreductive radical prostatectomy is to eliminate lethal clones ofcastration-resistant intraprostatic PCa, which can favor the process of metastasis (A Heidenreich et al. Current Opinion in Urology 2020), in order to improve OS and PFS and to prevent local progression and correlated events. Methods: APPROACH is an Italian multicenter study, which is enrolling ~566 pts with oligometastatic hormone sensitive prostate cancer who are candidates to receive treatment with apalutamide. After 6 months from the start of treatment, patients will be randomized 1:1 to receive local treatment or not in addition to apalutamide (investigator's choice between primary radiotherapy and cytoreductive prostatectomy). Primary end point: To determine whether treatment with apalutamide plus ADT for 6 months followed by locoregional treatment with radiotherapy or radical prostatectomy has better efficacy than treatment with apalutamide plus ADT alone in terms of radiographic progression-free survival (rPFS). Secondary end points: To evaluate tumor shrinkage after locoregional approach and to evaluate short and long-term side effects after locoregional surgery or RT, time to PSA progression, time to castration resistance, cancer specific survival, overall survival and quality of life according to EPIC-26 and EQ-5D-5L questionnaires. Clinical trial information: NCT05649943.

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Abstract Details

Meeting

2023 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Genitourinary Cancer—Prostate, Testicular, and Penile

Track

Genitourinary Cancer—Prostate, Testicular, and Penile

Sub Track

Prostate Cancer– Advanced/Hormone-Sensitive

Clinical Trial Registration Number

NCT05649943

Citation

J Clin Oncol 41, 2023 (suppl 16; abstr TPS5115)

DOI

10.1200/JCO.2023.41.16_suppl.TPS5115

Abstract #

TPS5115

Poster Bd #

200b

Abstract Disclosures