Feasibility and Impact of Liquid Biopsy Genomic Profiling on Treatment Patients With Metastatic Prostate Cancer in Spain (SOLTI-2102)
About this study
HOPE Prostate is an observational study that aims at promoting research against metastatic prostate cancer by means of collective research led by patients (patient-centric trial). Patients with metastatic prostate cancer living in Spain will voluntarily register and fulfil their journey in the study through the study's digital tool. Mainly they are prompted to answer questionnaires about their disease, and to provide a blood sample and an archival tumor biopsy. In HOPE Prostate these samples will be genomically analyzed and every patient case will be presented in a multidisciplinary molecular advisory board (MAB). The MAB will issue a plain report explaining the significance of the results and will try to enumerate future therapeutic options that match patient history and his genomic profile. Finally, patients will have to answer short follow-up questionnaires twice a year for 3 years. The study data will allow us to advance implementing precision medicine to improve the management of current and specially future metastatic prostate cancer patients.
- Condition
- Metastatic Prostate Cancer
- Tested
- Liquid Biopsy, Archival Tumor DNA sequencing
- Sponsor
- SOLTI Breast Cancer Research Group
Who can join
- Age
- 18 years and older
- Sex
- Male only
- Healthy volunteers
- Not accepted
Inclusion 9
- Minimum age: 18 years
- Eligible sex: Male
- Study condition: Metastatic Prostate Cancer
- Male patients living in Spain.
- Age ≥18 years.
- Signed informed consent before any screening procedure.
- Metastatic PC of any subtype confirmed both pathologically and radiologically (stage IV disease).
- The subjects must be about to receive, or receiving, or will have completed treatment for their metastatic disease with any line of treatment in either a clinical trial or the standard of care healthcare setting.
- Eastern Cooperative Oncology Group (ECOG) 0-1.
Exclusion 2
- Inability to consent or conform to the processes involved in a clinical study.
- Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
Where
1 site, 1 recruiting
SOLTI Cancer Research Group
Barcelona, Spain
Potential match only. Final eligibility is determined by the study team.