Molecular Biology Analysis for Para-aortic Nodes in the Ultra-staging of Advanced Cervical Cancers (GYNOSNA)
Primary Purpose
Advanced Cervical Cancer
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
'OSNA stadification during surgery'
Sponsored by
About this trial
This is an interventional other trial for Advanced Cervical Cancer
Eligibility Criteria
Inclusion Criteria:
- Women aged 18 or over
- Cervical cancer of any histological type
- Cervical cancer of advanced stage (>= IB2)
- negative para-aortic routine PET CT scan
- Patient affiliated to a social protection scheme
- Information on the study delivered to the patient
Exclusion Criteria:
- Patients minor
- Patient pregnant or breastfeeding or of childbearing age without effective contraception
- Other concurrent cancer or history of cancer (in the 5 years preceding the entry into the trial), except in situ cervical cancer treated basal cell or squamous cell or treated carcinoma
- Legal incapacity or limited legal capacity. medical or psychological conditions not allowing the subject to understand the study and sign the consent
Sites / Locations
- ICO René Gauducheau
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
OSNA stadification during surgery
Arm Description
The para-aortic dissection surgery is performed in the usual way. The lymph nodes are isolated from fat tissue during surgery, and will be analysis both by histological analysis and OSNA analysis
Outcomes
Primary Outcome Measures
compare the performance of OSNA for the detection of lymph node metastases in advanced cervical cancer
The main objective is to compare the performance of OSNA to both conventional methods and intensive histological analysis, for the detection of lymph node metastases in advanced cervical cancer.
The evaluation criteria is :
Determination of number of lymph node metastases expressed in a size in mm for conventional and intensive histological analysis.
Determination of the number of lymph node metastases expressed in a number of copies in molecular biology.
Secondary Outcome Measures
Full Information
NCT ID
NCT02888717
First Posted
August 30, 2016
Last Updated
March 23, 2020
Sponsor
Institut Cancerologie de l'Ouest
1. Study Identification
Unique Protocol Identification Number
NCT02888717
Brief Title
Molecular Biology Analysis for Para-aortic Nodes in the Ultra-staging of Advanced Cervical Cancers
Acronym
GYNOSNA
Official Title
Concordance Study of Molecular Biology Analysis for Para-aortic Nodes in the Ultra-staging of Advanced Cervical Cancers (GYNOSNA)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
April 28, 2015 (Actual)
Primary Completion Date
November 13, 2018 (Actual)
Study Completion Date
November 13, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut Cancerologie de l'Ouest
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The para-aortic lymph node involvement in the advanced stage of cervical cancer is a poor prognostic factor for overall survival. Concomitant chemo-radiotherapy has become the standard treatment for advanced cervical cancer. In case of para-aortic lymph node involvement, an extension of radiotherapy fields is recommended.
A prospective multicentre study shown that the survival rate of patients with node ≤ 5 mm and which benefited from the expansion of radiotherapy fields was identical to the survival of pN0 patients.
However, due to a specific disease, this technique should not be performed in all patients. It is necessary to reliably select patients with retroperitoneal lymph node involvement. For this, it is recommended that prior to the concurrent chemo-radiotherapy, nodal staging surgery with a definitive histological analysis.
So we propose to use molecular diagnostic test OSNA (One Step Nucleic Acid Amplification) to improve lymph node metastasis detection sensitivity to achieve ultra-staging compared to conventional histology.
Detailed Description
The para-aortic lymph node involvement in the advanced stage of cervical cancer is a poor prognostic factor for overall survival. Concomitant chemoradiotherapy has become the standard treatment for advanced cervical cancer. In case of para-aortic lymph node involvement, an extension of radiotherapy fields is recommended.
A prospective multicenter study shown that the survival rate of patients with node ≤ 5 mm and which benefited from the expansion of radiotherapy fields was identical to the survival of pN0 patients.
However, due to a specific disease, this technique should not be performed in all patients. It is necessary to reliably select patients with retroperitoneal lymph node involvement. For this, it is recommended that prior to the concurrent chemoradiotherapy, nodal staging surgery with a definitive histological analysis.
So we suggest using molecular diagnostic test OSNA (One Step Nucleic Acid Amplification) to improve lymph node metastasis detection sensitivity to achieve ultra-staging compared to conventional histology.
We propose to consider a new concordance study to assess the feasibility of the technical OSNA in a new indication: cervical cancer.
The analysis protocol of a concordance study is the same regardless of the location of the cancer. We evaluate the use of OSNA in order to ultrastaging of lymph node involvement for patients with advanced cancer of the cervix.
Our hypothesis is that OSNA would be:
better than the usual histological staging method
and equivalence in terms of sensitivity and specificity compared to intensive histological method To complete this study we propose to search the initial brain tumor expression of cytokeratin 19.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Cervical Cancer
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
OSNA stadification during surgery
Arm Type
Experimental
Arm Description
The para-aortic dissection surgery is performed in the usual way. The lymph nodes are isolated from fat tissue during surgery, and will be analysis both by histological analysis and OSNA analysis
Intervention Type
Procedure
Intervention Name(s)
'OSNA stadification during surgery'
Intervention Description
The para-aortic dissection surgery is performed in the usual way. The lymph nodes are isolated from fat tissue during surgery, and cut into 4 slices sterile.
Slices A and C are sent OSNA analysis
Slices B and D are sent ultimately histological analysis (1 cup HES or 5 cup HES + IHC) The nodes of less than 5 mm will be sent in final histological analysis due to the inability to cut into 4.
After the analysis, the report indicates whether the node is:
Free (-): <250 copies
Micrometastatic (+): 250 ≤ - <5,000 copies,
Macrometastatic (++): ≥ 5000 copies.
Primary Outcome Measure Information:
Title
compare the performance of OSNA for the detection of lymph node metastases in advanced cervical cancer
Description
The main objective is to compare the performance of OSNA to both conventional methods and intensive histological analysis, for the detection of lymph node metastases in advanced cervical cancer.
The evaluation criteria is :
Determination of number of lymph node metastases expressed in a size in mm for conventional and intensive histological analysis.
Determination of the number of lymph node metastases expressed in a number of copies in molecular biology.
Time Frame
15 days between surgery and OSNA results
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women aged 18 or over
Cervical cancer of any histological type
Cervical cancer of advanced stage (>= IB2)
negative para-aortic routine PET CT scan
Patient affiliated to a social protection scheme
Information on the study delivered to the patient
Exclusion Criteria:
Patients minor
Patient pregnant or breastfeeding or of childbearing age without effective contraception
Other concurrent cancer or history of cancer (in the 5 years preceding the entry into the trial), except in situ cervical cancer treated basal cell or squamous cell or treated carcinoma
Legal incapacity or limited legal capacity. medical or psychological conditions not allowing the subject to understand the study and sign the consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JAFFRE Isabelle, MD
Organizational Affiliation
Institut de Cancérologie de l'Ouest
Official's Role
Principal Investigator
Facility Information:
Facility Name
ICO René Gauducheau
City
Saint-Herblain
ZIP/Postal Code
44805
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Molecular Biology Analysis for Para-aortic Nodes in the Ultra-staging of Advanced Cervical Cancers
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