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Detection of Tumor Associated Cell-free DNA in Peritoneal Fluid Obtained by Culdocentesis

Primary Purpose

Stage III Ovarian Cancer, Stage IV Ovarian Cancer

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Culdocentesis
Vaginal Swab
Chromopertubation
Blood collection
Tissue collection
Sponsored by
Dana-Farber Cancer Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Stage III Ovarian Cancer focused on measuring Stage III Ovarian Cancer, Stage IV Ovarian Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Female
  • Age ≥ 18
  • Able to give informed consent
  • Scheduled for surgery at Brigham and Women's Hospital for known or highly suspected Stage III or IV ovarian cancer (i.e. elevated CA-125 with a pelvic mass, ascites, and carcinomatosis)
  • Post-menopausal or negative urine and/or blood pregnancy test
  • Measurable disease on preoperative imaging

Exclusion Criteria:

  • Male
  • Age < 18
  • Unable to give informed consent
  • Not planned for surgical intervention
  • Active malignancy other than ovarian cancer
  • Prior bilateral tubal ligation or hysterectomy (as this would prevent chromopertubation)
  • Known or suspected active pelvic infection
  • Pregnancy
  • No measurable disease or suspected Stage I or II ovarian cancer on preoperative imaging

Sites / Locations

  • Brigham and Women's Hospital
  • Dana Farber Cancer Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Culdocentesis

Arm Description

Patients with known or highly likely ovarian cancer (i.e. highly elevated CA-125, ascites, pelvic mass) scheduled for cytoreductive surgery will be identified during preoperative consultation and offered participation in the study. During Surgery: Blood Collection Vaginal Swab Chromopertubation Culdocentesis Tissue Collection

Outcomes

Primary Outcome Measures

Number of completed peritoneal fluid collection by culdocentesis after chromopertubation as an assessment of feasibility of peritoneal fluid collection in women with ovarian cancer.

Secondary Outcome Measures

Measure the concentration of cell free DNA in various biologic fluids and compare it to primary tumor DNA.

Full Information

First Posted
April 14, 2015
Last Updated
May 1, 2020
Sponsor
Dana-Farber Cancer Institute
Collaborators
Celula, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02441140
Brief Title
Detection of Tumor Associated Cell-free DNA in Peritoneal Fluid Obtained by Culdocentesis
Official Title
Detection of Tumor Associated Cell-free DNA in Peritoneal Fluid Obtained by Culdocentesis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Terminated
Why Stopped
Poor accrual
Study Start Date
May 2015 (undefined)
Primary Completion Date
July 2019 (Actual)
Study Completion Date
July 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dana-Farber Cancer Institute
Collaborators
Celula, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research study is studying a possible test which may help doctors diagnose women with ovarian cancer.
Detailed Description
This research study is a Feasibility Study, to try to evaluate whether or not culdocentesis can detect tumor associated cell free DNA. Although this is the first time investigators are using this type of procedure to detect cell free DNA, culdocentesis is not a new procedure. It used to be done routinely in the past to examine pelvic fluid. The investigator's goal is to develop a test to detect ovarian cancer in women before they develop any signs or symptoms of the disease. Currently, there is no screening test for ovarian cancer. This study uses a technique called "culdocentesis" to detect DNA released by ovarian cancer cells into pelvic fluid. During culdocentesis, a small needle is inserted through the vagina into an empty space between the uterus and the rectum called the "cul-de-sac." Fluid is withdrawn from this space and sent for analysis. Culdocentesis is a technique that has been used for many years to examine pelvic fluid and determine its composition, but it has not previously been studied as a technique for examining cell-free DNA to detect ovarian cancer. The investigators suspect that this may be a useful way to detect cell-free DNA from ovarian cancer cells because the ovaries are very close to the cul-de-sac space. In this study, the investigators will compare our ability to detect cell-free DNA in fluid from the cul-de-sac with our ability to detect cell-free DNA from a vaginal swab (similar to a Pap smear), a blood test, and in the tissue specimens collected at the time of surgery. The investigators are hoping to learn from this study whether developing a cell-free DNA test to screen for ovarian cancer involving culdocentesis would be an effective strategy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stage III Ovarian Cancer, Stage IV Ovarian Cancer
Keywords
Stage III Ovarian Cancer, Stage IV Ovarian Cancer

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Culdocentesis
Arm Type
Experimental
Arm Description
Patients with known or highly likely ovarian cancer (i.e. highly elevated CA-125, ascites, pelvic mass) scheduled for cytoreductive surgery will be identified during preoperative consultation and offered participation in the study. During Surgery: Blood Collection Vaginal Swab Chromopertubation Culdocentesis Tissue Collection
Intervention Type
Procedure
Intervention Name(s)
Culdocentesis
Intervention Description
A sterile speculum will be placed in the vagina and the cervix identified. The cervix will be elevated using a tenaculum and a spinal needle inserted through the posterior vaginal fornix. Fluid from the posterior cul de sac will be collected
Intervention Type
Procedure
Intervention Name(s)
Vaginal Swab
Intervention Description
. A sterile speculum will be placed in the vagina and a Pap smear spatula will be used to swab the posterior fornix of the vagina. This swab will then be rinsed in a tube of saline.
Intervention Type
Procedure
Intervention Name(s)
Chromopertubation
Intervention Description
Chromopertubation is a common gynecologic technique used to test the patency of fallopian tubes during infertility evaluations. Fluid is flushed through the cervix and uterus and out the fallopian tubes.
Intervention Type
Procedure
Intervention Name(s)
Blood collection
Intervention Description
Intravenous blood collection will be drawn from an IV
Intervention Type
Procedure
Intervention Name(s)
Tissue collection
Intervention Description
As part of the standard surgical procedure for presumed ovarian cancer, the primary tumor will be resected and a sample obtained for evaluation
Primary Outcome Measure Information:
Title
Number of completed peritoneal fluid collection by culdocentesis after chromopertubation as an assessment of feasibility of peritoneal fluid collection in women with ovarian cancer.
Time Frame
At the time of surgery
Secondary Outcome Measure Information:
Title
Measure the concentration of cell free DNA in various biologic fluids and compare it to primary tumor DNA.
Time Frame
At the time of surgery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female Age ≥ 18 Able to give informed consent Scheduled for surgery at Brigham and Women's Hospital for known or highly suspected Stage III or IV ovarian cancer (i.e. elevated CA-125 with a pelvic mass, ascites, and carcinomatosis) Post-menopausal or negative urine and/or blood pregnancy test Measurable disease on preoperative imaging Exclusion Criteria: Male Age < 18 Unable to give informed consent Not planned for surgical intervention Active malignancy other than ovarian cancer Prior bilateral tubal ligation or hysterectomy (as this would prevent chromopertubation) Known or suspected active pelvic infection Pregnancy No measurable disease or suspected Stage I or II ovarian cancer on preoperative imaging
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Neil Horowitz, MD
Organizational Affiliation
Dana-Farber Cancer Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Dana Farber Cancer Institute
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Detection of Tumor Associated Cell-free DNA in Peritoneal Fluid Obtained by Culdocentesis

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