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Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer (EPIDROP) (EPIDROP)

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Blood sample
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring Circulating tumor cells (CTCs), Biomarker, CellSearch, EPIDROP

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria :

  • To be male, over 18 years old
  • Metastatic prostate cancer naive to any treatment or metastatic prostate cancer in biological recurrence (PSA increase) and/or clinical recurrence after hormone suppression (mCRPC)

Exclusion Criteria:

  • Non-metastatic prostate cancer in biological and/or clinical recurrence after hormone-suppression (nmCRPC)
  • Other active or treated cancer less than 5 years old
  • Be protected by law (guardianship or curatorship)
  • Be deprived of liberty by administrative decision
  • Not being affiliated to a social security scheme, or not being a beneficiary of such a plan
  • Being in a period of exclusion from another protocol
  • Inability to understand and/or respond to questionnaires
  • Inability to understand the nature, purpose and methodology of the study
  • Refusal to sign informed consent

Sites / Locations

  • University Hospital Center
  • University Center, HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Patients with metastatic prostate cancer

Arm Description

Outcomes

Primary Outcome Measures

EPIDROP technique sensitivity versus CellSearch system sensitivity
Proportion of true positive and false negative patients with a confidence interval
EPIDROP technique specificity versus CellSearch system specificity
Proportion of true negative and false positive healthy controls with a confidence interval

Secondary Outcome Measures

Full Information

First Posted
October 2, 2020
Last Updated
June 2, 2021
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT04581109
Brief Title
Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer (EPIDROP)
Acronym
EPIDROP
Official Title
Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 27, 2021 (Actual)
Primary Completion Date
April 2022 (Anticipated)
Study Completion Date
October 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The use of liquid biopsy could be the key for precision medicine. Circulating tumor cells (CTCs) are the most studied circulating biomarkers used to assess the metastatic process and they have shown their clinical validity and utility in cancer patients. However, their detection and capture are still a challenge as they are very rare in the bloodstream. In this clinical trial named "EPIDROP", the investigators will use an innovative device called EPIDROP (for EPIspot in a DROP) in metastatic prostate cancer. EPIDROP is a completely new technology answering to biological and clinical questions by proposing a procedure detecting the functional subset of prostatic CTCs at the single cell level. The investigators will stain cells in the sample for EpCAM, PSMA, CD45 before to encapsulate them one by one in microdroplets and measure the PSA secretion by only the viable CTCs. This study aims to demonstrate the non-inferiority of the EPIDROP compared to the CellSearch system.
Detailed Description
Methods : One hundred patients with a metastatic prostate cancer will be recruited plus 50 healthy donors. Twenty ml of blood will be drawn : 10 ml of blood will be drawn on CellSave tubes (fixed cells) for CTC detection using the FDA-cleared CellSearch system (gold standard) and 10 ml of blood will be drawn on EDTA tubes (viable cells) for the detection of functional CTCs using the EPIDROP. Patients will be followed for 18 months. Samples from fifty control subjects will be provided by the Etablissement Français du Sang.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Circulating tumor cells (CTCs), Biomarker, CellSearch, EPIDROP

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Patients with metastatic prostate cancer
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
Blood sample
Intervention Description
Twenty ml of blood will be drawn from each patient : 10 ml of blood will be drawn on CellSave tubes (fixed cells) for CTC detection using the FDA-cleared CellSearch system (gold standard) and 10 ml of blood will be drawn on EDTA tubes (viable cells) for the detection of functional CTCs using the EPIDROP.
Primary Outcome Measure Information:
Title
EPIDROP technique sensitivity versus CellSearch system sensitivity
Description
Proportion of true positive and false negative patients with a confidence interval
Time Frame
At 18 months
Title
EPIDROP technique specificity versus CellSearch system specificity
Description
Proportion of true negative and false positive healthy controls with a confidence interval
Time Frame
At 18 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria : To be male, over 18 years old Metastatic prostate cancer naive to any treatment or metastatic prostate cancer in biological recurrence (PSA increase) and/or clinical recurrence after hormone suppression (mCRPC) Exclusion Criteria: Non-metastatic prostate cancer in biological and/or clinical recurrence after hormone-suppression (nmCRPC) Other active or treated cancer less than 5 years old Be protected by law (guardianship or curatorship) Be deprived of liberty by administrative decision Not being affiliated to a social security scheme, or not being a beneficiary of such a plan Being in a period of exclusion from another protocol Inability to understand and/or respond to questionnaires Inability to understand the nature, purpose and methodology of the study Refusal to sign informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine ALIX-PANABIERES, MCU-PH
Phone
04 11 75 99 31
Ext
+33
Email
c-panabieres@chu-montpellier.fr
Facility Information:
Facility Name
University Hospital Center
City
Montpellier
State/Province
Occitanie
ZIP/Postal Code
34295
Country
France
Individual Site Status
Active, not recruiting
Facility Name
University Center, Hospital
City
Nîmes
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephane DROUPY, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer (EPIDROP)

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