Predictive Value of microRNA in Thyroid Cytologies of Undetermined Type (PREDICYTHY)
Primary Purpose
Thyroid Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Signature of microRNA for patients with bethesda classification 3, 4 or 5
Sponsored by
About this trial
This is an interventional diagnostic trial for Thyroid Cancer
Eligibility Criteria
Inclusion Criteria:
- Man or woman whose Age is ≥ 18 years
- Patient requiring ultrasound for thyroid nodule scanning with established indication of FNAC
- Patient with Bethesda 3, 4 and 5 thyroid nodule
- Informed patient and signed informed consent received
- Patient affiliated to a French medical coverage system
Exclusion Criteria:
- Patient under guardianship, curatorship or safeguarding of justice
- Patient whose medical or psychological conditions do not permit them to complete the study or to sign the consent,
- Patient with metastatic cancer distinct from thyroid cancer
- Patient who has stopped treatment (chemotherapy / immunotherapy) for cancer for less than 6 months.
Sites / Locations
- CHU de ToulouseRecruiting
- Institut régional du Cancer de MontpellierRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Signature of microRNA
Arm Description
Signature of miRNA in patients with Thyroid Cytologies of undetermined type and with a Bethesda classification 3, 4 or 5
Outcomes
Primary Outcome Measures
Area under receiver operating characteristic (ROC) curve of the microRNA signature
Secondary Outcome Measures
Sensitivity of the test (microRNA)
Sensitivity is defined as the proportion of patients with a malignant nodule (diagnosed by the gold standard method) and a positive test with miRNA signature.
Specificity of the test (microRNA)
The specificity of the test is defined as the proportion of patients with a benign nodule (diagnosed by the gold standard method) and a negative test with miRNA signature.
Positive predictive value (PPV) of the test (microRNA)
The positive predictive value is defined as the probability that the patient with a positive test is actually affected by a malignant nodule (diagnosed by the gold standard method).
Negative predictive value (NPV) of the test (microRNA)
The negative predictive value is defined as the probability that the patient with a negative test is actually affected by a benign nodule (diagnosed by the gold standard method).
Full Information
NCT ID
NCT04285476
First Posted
February 24, 2020
Last Updated
June 6, 2023
Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
1. Study Identification
Unique Protocol Identification Number
NCT04285476
Brief Title
Predictive Value of microRNA in Thyroid Cytologies of Undetermined Type
Acronym
PREDICYTHY
Official Title
Study of the Predictive Value of a Signature of microRNA in Thyroid Cytologies of Undetermined Type
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 17, 2021 (Actual)
Primary Completion Date
July 2026 (Anticipated)
Study Completion Date
December 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
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 aim is to validate a signature of microRNA (micro Ribonucleic acid) based in a first exploratory study allowing the stratification of the cytologies of indeterminate type and to study and select others. In a first step, the teams will focus on standardising the pre-analytical stages and defining a threshold of positivity. The results of microRNA signature on a cohort of 70 patients will be compared with the ultrasound and then histological data of the resection specimen.
Detailed Description
Morphological analysis of fine-needle aspiration cytology (FNAC) under ultrasound classifies thyroid nodules in 6 categories (Bethesda classification). The diagnostic approach is codified by the Society of Endocrinology and for cytologies of indeterminate type (Bethesda 3, 4 and 5), surgery of thyroid nodules is currently recommended. However, only 15.9% of the cytologies classified Bethesda 3, 26.1% of the Bethesda IV and 75.2% of the Bethesda V are actually cancers in the definitive histological analysis on surgical resection.
Thus, new tools for predicting the risk of thyroid nodule malignancy need to be developed.
To date, various risk stratification biomarkers have been reported in the literature but have not been validated in independent cohorts, thus excluding their implementation in daily practice.
In addition, two commercial nucleic acid tests are proposed at a cost not compatible with generalized diffusion. The first approach is based on a next generation sequencing analysis of a target gene panel at the nucleotide sequence or transcribed level. The second alternative combines an analysis at level 1) of the deoxyribonucleic acid (DNA) with the search for somatic variations such as mutations in oncogenes or the presence of fusion genes, and 2) microRNA with the measurement of their level of expression.
Due to their stability, their ability to modulate the expression of various messenger RNA, microRNA are an attractive line of research.
The aim is to validate a signature of microRNA based in a first exploratory study allowing the stratification of the cytologies of indeterminate type and to study and select others. In a first step, the teams will focus on standardising the pre-analytical stages and defining a threshold of positivity. The results of microRNA signature on a cohort of 70 patients will be compared with the ultrasound and then histological data of the resection specimen.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thyroid 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
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Signature of microRNA
Arm Type
Experimental
Arm Description
Signature of miRNA in patients with Thyroid Cytologies of undetermined type and with a Bethesda classification 3, 4 or 5
Intervention Type
Diagnostic Test
Intervention Name(s)
Signature of microRNA for patients with bethesda classification 3, 4 or 5
Intervention Description
If the cytology results are Bethesda 3, 4 or 5, then a miRNA analysis will be performed.
Primary Outcome Measure Information:
Title
Area under receiver operating characteristic (ROC) curve of the microRNA signature
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Sensitivity of the test (microRNA)
Description
Sensitivity is defined as the proportion of patients with a malignant nodule (diagnosed by the gold standard method) and a positive test with miRNA signature.
Time Frame
24 months
Title
Specificity of the test (microRNA)
Description
The specificity of the test is defined as the proportion of patients with a benign nodule (diagnosed by the gold standard method) and a negative test with miRNA signature.
Time Frame
24 months
Title
Positive predictive value (PPV) of the test (microRNA)
Description
The positive predictive value is defined as the probability that the patient with a positive test is actually affected by a malignant nodule (diagnosed by the gold standard method).
Time Frame
24 months
Title
Negative predictive value (NPV) of the test (microRNA)
Description
The negative predictive value is defined as the probability that the patient with a negative test is actually affected by a benign nodule (diagnosed by the gold standard method).
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Man or woman whose Age is ≥ 18 years
Patient requiring ultrasound for thyroid nodule scanning with established indication of FNAC
Patient with Bethesda 3, 4 and 5 thyroid nodule
Informed patient and signed informed consent received
Patient affiliated to a French medical coverage system
Exclusion Criteria:
Patient under guardianship, curatorship or safeguarding of justice
Patient whose medical or psychological conditions do not permit them to complete the study or to sign the consent,
Patient with metastatic cancer distinct from thyroid cancer
Patient who has stopped treatment (chemotherapy / immunotherapy) for cancer for less than 6 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Moussion Aurore
Phone
0467612446
Ext
+33
Email
aurore.moussion@icm.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Texier Emmanuelle
Phone
0467613102
Email
emmanuelle.texier@icm.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Riviere Christine, MD
Organizational Affiliation
Institut régional du Cancer de Montpellier
Official's Role
Study Chair
Facility Information:
Facility Name
CHU de Toulouse
City
Toulouse
State/Province
Haute-Garonne
ZIP/Postal Code
31000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Frédérique Savagner, MD
Phone
567690375
Ext
+33
Email
savagner.f@chu-toulouse.fr
Facility Name
Institut régional du Cancer de Montpellier
City
Montpellier
State/Province
Hérault
ZIP/Postal Code
34298
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chritine Rivière, MD
Phone
467618522
Ext
+33
Email
christine.riviere@icm.unicancer.fr
12. IPD Sharing Statement
Plan to Share IPD
No
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Predictive Value of microRNA in Thyroid Cytologies of Undetermined Type
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