Radio Guided Lymph Node Dissection in Oligometastatic Prostate Cancer Patients

Prostate Cancer Clinical Trial

— DETECT  

Official title:

Radio Guided Lymph Node Dissection in Oligometastatic Prostate Cancer Patients

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04300673
• Other study ID #: 2019-5805
• Secondary ID: 2019-003284-21
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• Start date: September 1, 2020
• Est. completion date: April 1, 2023

Study information

• Verified date: April 2022
• Source: Radboud University Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is a prospective, single arm phase I/II study. The primary aim of this study is to evaluate the feasibility of 111In-PSMA I&T radio guided surgery in patients diagnosed with prostate cancer who are highly suspected of having one or more pelvic lymph node metastases based on pre-operative imaging.

Patients with prostate cancer who have a high risk of lymph node metastases based on PSMA PET/CT and scheduled for robot-assisted PLND (with or without prostatectomy) will be recruited. Eligible patients will receive an additional ferumoxtran-10 enhanced MRI to complement pre-operative imaging. Twenty-four hours before surgery, patients will receive the radiolabelled PSMA tracer. Pelvic Lymph node dissections are carried out according to standard of care procedures. During surgery, the surgeon will be provided with a gamma-probe to detect PSMA expressing lymph nodes in vivo. Dissected samples will be systematically assessed on tracer accumulation using the gamma-probe ex vivo. After surgery, the samples will be scanned in the small animal SPECT/CT and 7T-MRI. After scanning, samples will be presented to pathologists for pathological analysis according to standard of care including staining for PSMA expression. At 3 months after surgery, patients will undergo a PSMA-PET/CT. Up until one year after surgery patients will be followed according to standard of care-guidelines by 3-monthly serum-PSA measurements.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 20
• Est. completion date: April 1, 2023
• Est. primary completion date: April 1, 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 50 Years and older

Eligibility

Inclusion Criteria:

• Histologically proven cancer of the prostate, based on prostate biopsy-core analysis.

• At least one 18F/68Ga-PSMA-PET/CT suspected positive metastasis in lymph nodes, located in the pelvic region.

• Patient is scheduled and fit for robot assisted surgery (PLND or radical prostatectomy +PLND).

• Patient is suitable for PLND (and radical prostatectomy) conform institutional guidelines and is not yet treated pre-operatively .

• Age=50 years.

• Ability to give voluntary written informed consent to participate in this study.

Exclusion Criteria:

• No detectable lesion on the 18F/68Ga-PSMA-PET/CT with an uptake level above liver uptake level (reference).

• Patients who are not scheduled for robot-assisted PLND.

• Prior pelvic surgery(1)

• Unequivocal evidence of metastases outside the pelvic region.

• Presence of any medical condition that in the opinion of the investigator/treating physician will affect patients' clinical status by participating in this trial.

• Prior prostate cancer treatment(2).

• Contraindication for MRI-scanning, i.e. claustrophobia, intracranial metal clips, metallic bodies in the eye, implanted electric and electronic devices not eligible for MRI (pacemakers, insulin pumps, cochlear implants, neurostimulators).

• Inability to lie still for at least 60 minutes or comply with imaging.

• Contraindication for iron infusion or hypersensitivity/allergy to the active substance or any of the excipients.

• The patient is already enrolled in one or more concurrent studies, which could confound the results of this study, according to the investigators.

1. Pelvic surgery is defined as "any surgery associated with pelvic lymphadenopathy'.

2. Prior prostate cancer treatment is defined as prostate and/or pelvic radiotherapy, hormonal treatments such as androgen deprivation therapy, prostate brachytherapy, prostate cryotherapy, high intensity focused ultrasound (HIFU) and/or prostate electroporation.

Related Conditions & MeSH terms

• Lymph Node Metastases
• Lymphatic Metastasis
• Prostate Cancer
• Prostatic Neoplasms

Intervention

Procedure:
• Radio guided surgery (RGS) using Indium-labelled PSMA
Approximately 24hours prior to surgery (PLND) patients receive a radiolabelled PSMA-tracer. During surgery, urologists will use a gamma-probe to detect PSMA-postitive tumour depostitions in pelvic lymph nodes.

Locations

Country	Name	City	State
Netherlands	Canisius Wilhelimina Ziekenhuis	Nijmegen
Netherlands	Radboudumc	Nijmegen	Gelderland

Sponsors (1)

Lead Sponsor	Collaborator
Radboud University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of 111In-PSMA-I&T radio guided surgery	The primary aim of this study is to evaluate the feasibility of 111In-PSMA-I&T radio guided surgery in patients diagnosed with prostate cancer who are highly suspected of having one or more pelvic lymph node metastasis/metastases based on pre-operative imaging. Feasibility will be defined as the ability to intra-operatively detect the lymph nodes (using a gamma probe) which were pre-operatively identified on PSMA-PET/CT	1 year
Secondary	The accuracy of 111In-PSMA-I&T radio guided surgery	Accuracy will be expressed as sensitivity and specificity percentage. Test results of gamma probe (positive or negative) will be compared with histopathology (gold standard) (positive or negative: i.e. containing PSMA-expressing prostate cancer cells).	1 year
Secondary	The safety of 111In-PSMA-I&T	Safety will be assesed by the number of participants with treatment related adverse events as assessed by CTCAE v4.0. For this outcome measure extra bloodsampling is included in the study protocol.	1 year
Secondary	Dosimetry of 111In-PSMA-I&T	Blood-clearance ratios will be determined based on radiation dosimetry as assessed by bloodsampling at set time points after injection.	1 year
Secondary	Correlation between tracer accumulation and lymph node size, PSMA-staining and SUV on PSMA-PET/CT		1 year
Secondary	Correlation between post-operative nano-MRI and SPECT		1 year
Secondary	Correlation between pre-operative imaging and postoperative imaging		2 years