RecruitingNCT06060652

Prostate Oligometastatic Cancer Management Driven by Disease Biology et/or Immunoactivity (PROMETEO)


Sponsor

Centro di Riferimento Oncologico - Aviano

Enrollment

104 participants

Start Date

May 11, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Currently, despite the advent of next-generation imaging has improved the detection of Oligometastatic prostate cancer (OMPC), prognostic biomarkers able to stratify patients and monitor treatment response are lacking and urgently needed. Mounting evidence suggests that molecular profiling of the disease and host immune activity evaluation can reveal OMPC heterogeneity and address the above unmet clinical need. This study aims at combining the analysis of several biomarkers to improve the prognostic stratification of OMPC patients


Eligibility

Sex: MALEMin Age: 18 Years

Inclusion Criteria19

  • Retrospective cohort
  • \>18 years old;
  • Patients previously included in the ADAPT-CTC trial
  • Prospective cohort
  • \>18 years old
  • Histologic confirmation (primary or metastatic tumor) of Acinar Adenocarcinoma of Prostate
  • Hormone-sensitive OMPC defined as ≤3 metachronous metastases (bone and/or lymph node) detected within the past 6 months with Choline/PSMA PET-CT following prostate specific antigen (PSA) rising after primary treatment (surgery and/or radiotherapy) with curative intent as defined by European Association of Urology criteria (EAU).
  • Controlled primary tumor
  • Prior salvage treatment to the primary prostate cancer is allowed.
  • PSA ≤ 50 ng/mL
  • Testosterone ≥ 0.5 ng/mL
  • ADT associated to the primary treatment concluded more than 6 months prior to the enrollment.
  • Patients eligible for a course of SBRT on bone and/or lymph node metastatic sites
  • Patients must have a life expectancy ≥ 12 months and an ECOG performance status ≤ 2
  • Patients must have normal organ and marrow function defined as:
  • Leukocytes ≥2000/µL
  • Absolute Neutrophil Count ≥1000/µL
  • Platelets ≥50000/µL
  • Patients amenable to understand and sign written informed consent documents

Exclusion Criteria12

  • Prospective cohort
  • Spinal cord compression or impending spinal cord compression.
  • Suspected pulmonary and/or liver metastases
  • Patient receiving any other investigational agents
  • Patient is participating in a concurrent treatment protocol
  • Prior treatments for hormone-sensitive OMPC
  • Serum creatinine \> 3 times the upper limit of normal.
  • Total bilirubin \> 3 times the upper limit of normal.
  • Liver Transaminases \> 5-times the upper limit of normal.
  • Unable to lie flat during or tolerate PET/CT or SBRT.
  • Previous history of cancer other than non-melanoma skin cancer in the last 5 years
  • Traumatic bone events in the 4 weeks before PET

Locations(2)

IRCCS-Centro di Riferimento Oncologico (CRO) di Aviano

Aviano, Pordenone, Italy

ASST Spedali Civili

Brescia, Italy

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NCT06060652


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