Metastasis-directed Therapy in Oligoprogressive Castration-refractory Prostate Cancer

Inclusion Criteria

• •Participants eligible for inclusion in this Trial must meet all the following criteria:
• •Written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedures.
• •Acinar adenocarcinoma (inclusive neuro-endocrine dedifferentiation).
• •Oligoprogressive disease on conventional imagine within a maximum of 6 weeks prior to randomisation defined as: a maximum of 3 extracranial progressive lesions (pre-existing lesions, the development of new lesions, or both) in any organ. Nodal (N1) disease should be measured in the short axis. Nodes more than 1.5 cm in the short axis are considered pathologic and measurable. Oligoprogression on bone scan is defined as the occurrence of maximal 3 new and/or progressive lesions. In case of not unambiguously, additional imaging such as diagnostic magnetic resonance imaging (MRI) or dedicated CT-scan should be performed. Visceral disease reported separately (lung, liver, adrenal, or CNS) and is considered measurable if an individual lesions is more than 1 cm longest dimension.
• •In case of locally persistent/recurrent disease, a diagnostic MRI of the prostate (bed) and/or biopsy of the site is recommended. There are two different mCRPC patient groups who are eligible for inclusion in the trial:
• •1. Patients with oligoprogressive disease with pADT only as ongoing treatment (Type 1).
• •2. Patients with oligoprogressive disease with pADT +/- second line systemic therapy. This is both the combination of pADT + ARTA as ongoing treatment or patients who had received docetaxel in the past (Type 2).
• •* Castration-refractory disease, defined as testosterone level \< 50 ng/dL.
• •* Prior treatment of the primary tumor by radiotherapy or surgery. If the primary tumor has not been treated previously, this treatment is obligatory within the trial.
• •* WHO performance 0-2
• •* Age \>= 18 years old
• •* Absence of psychological, sociological, or geographical condition potentially hampering compliance with study protocol.
• •* Patients must be presented at the multidisciplinary board meeting and the inclusion in the trial needs approval by this board.