Retrospective Analysis of 68Ga-PSMA-PET in Patients With Prostate Cancer: Experience From Brazil

Prostate Cancer Clinical Trial

— PET-PSMA  

Official title:

Retrospective Analysis of 68Ga-PSMA-PET in Patients With Prostate Cancer: Experience From Brazil

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT05169372
• Other study ID #: LACOG 0121
• Status: Terminated
• Start date: May 11, 2022
• Est. completion date: January 19, 2024

Study information

• Verified date: February 2024
• Source: Latin American Cooperative Oncology Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Gallium-68-prostate-specific membrane antigen (68Ga-PSMA) positron emission tomography (PET) has been increasingly used in the management of PCa in Brazil. Thus, the detection of metastatic lesions is improved over traditional methods e.g. MRI and the diagnosis of mCSPC patients has been proportionally increasing. Due to a lack of guidelines and clinical trials including 68Ga-PSMA-PET imaging, the management of these patients is extrapolated from data based on conventional imaging. Treatment decision and duration of treatment for mCSPC patients based on 68Ga-PSMA-PET imaging is currently unknown. 68Ga-PSMA-PET allows a diagnosis of a different set of low volume oligo-metastatic prostate cancer patients. Based on that, a new gap has been built up, since there are no standards of how those patients are managed and how they respond to conventional therapies, to metastasis direct therapy or even if they could be spared of any treatment, reducing costs and toxicities. This patient population has not been included in clinical trials and its critical to generate information on the diagnosis, treatment and outcome of these patients in clinical practice.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 12
• Est. completion date: January 19, 2024
• Est. primary completion date: January 19, 2024
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age of at least 18 years at study entry;

2. Histologically confirmed adenocarcinoma of the prostate;

3. 68Ga-PSMA-PET exam performed between October 2015 and January 2021;

4. 68Ga-PSMA-PET performed in one of the following situations:

• localized disease at diagnosis in patients with no detection of extra-prostatic disease in traditional imaging such as CT scan, MRI and bone scan;

• biochemical recurrence (according to PCWG3 or defined by the investigator) in patients with no detection of prostatic or extra-prostatic disease in traditional imaging such as CT scan, MRI and bone scan;

5. Traditional imaging (pelvic and abdominal CT or MRI and bone scan) with negative results (no extra-prostatic disease, for localized and biochemical recurrence disease; no prostatic for biochemical recurrence disease) performed within 8 weeks before 68Ga-PSMA-PET;

6. Site and investigator ability to collect adequate patient characteristics, treatment and outcome data from medical records.

Exclusion Criteria:

1. Patients with no disease characteristics accessible in medical records;

2. Cancer diagnosis other than prostate cancer in the last 5 years;

3. Disease detected by traditional imaging techniques (bone scan, CT and/or MRI), meaning extra-prostatic disease, for localized and biochemical recurrence disease; or prostatic disease for biochemical recurrence disease.

Related Conditions & MeSH terms

• Prostate Cancer
• Prostatic Neoplasms

Locations

Country	Name	City	State
Brazil	CPO - Centro de Pesquisa em Oncologia do Hospital São Lucas da PUCRS	Porto Alegre	Rio Grande Do Sul
Brazil	HMV - Hospital Moinhos de Vento	Porto Alegre	Rio Grande Do Sul
Brazil	Instituto COI - Clínicas Oncológicas Integradas (Instituto Américas RJ)	Rio De Janeiro

Sponsors (2)

Lead Sponsor	Collaborator
Latin American Cooperative Oncology Group	Astellas Pharma Inc

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The rate of patients with 68Ga-PSMA-PET positive lesions	The rate of patients with 68Ga-PSMA-PET positive lesions [defined as the presence of lesions with 68Ga-PSMA uptake in the prostate (biochemical recurrence) and in extra-prostatic sites (localized disease and biochemical recurrence) in patients with no detected lesions in conventional imaging (no extra prostatic disease, for localized and biochemical recurrence disease; or prostatic disease for biochemical recurrence disease)]	January 2021
Secondary	68Ga-PSMA-PET prostate cancer confirmed detection rate	Defined as the proportion of patients with prostate cancer confirmed by histopathology or with PSA response (reduction = 50% on PSA levels from baseline) in those treated with lesion-directed therapy without ADT in day + 90)	January 2021
Secondary	Treatment patterns in evaluable patients based on 68Ga-PSMA-PET diagnostic status		January 2021
Secondary	The percentage of change in initial treatment plan considering the results of 68Ga-PSMA-PET in negative traditional imaging		January 2021
Secondary	To describe the type of disease monitoring imaging technique (i.e., CT scan, MRI, 68Ga-PSMA-PET) methods after initial diagnosis with 68Ga-PSMA-PET		January 2021
Secondary	Clinical effectiveness of first-line treatment based on 68Ga-PSMA-PET diagnostic status	(no extra-prostatic disease - localized disease or local recurrence); nodal positive/metastasis negative (regional disease) and metastasis positive (distant disease)	January 2021
Secondary	Treatment duration of first-line treatment based on 68Ga-PSMA-PET diagnostic status		January 2021