PREDICYTHY: Predictive Value of 10 microRNA in Thyroid Cytologies of Undetermined Type

Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle (Other)
Overall Status
Recruiting
CT.gov ID
NCT04285476
Collaborator
(none)
70
2
1
65.5
35
0.5

Study Details

Study Description

Brief Summary

The aim is to validate a signature of 10 microRNA (micro Ribonucleic acid) selected in a first exploratory study allowing the stratification of the cytologies of indeterminate type (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.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Signature of 10 microRNA for patients with bethesda classification 3, 4 or 5
N/A

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 10 microRNA selected in a first exploratory study allowing the stratification of the cytologies of indeterminate type (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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
70 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Study of the Predictive Value of a Signature of 10 microRNA in Thyroid Cytologies of Undetermined Type
Actual Study Start Date :
Jun 17, 2021
Anticipated Primary Completion Date :
Jul 1, 2026
Anticipated Study Completion Date :
Dec 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Signature of 10 microRNA

Signature of 10 miRNA in patients with Thyroid Cytologies of undetermined type and with a Bethesda classification 3, 4 or 5

Diagnostic Test: Signature of 10 microRNA for patients with bethesda classification 3, 4 or 5
If the cytology results are Bethesda 3, 4 or 5, then a miRNA analysis will be performed.

Outcome Measures

Primary Outcome Measures

  1. Area under receiver operating characteristic (ROC) curve of the 10 microRNA signature [24 months]

Secondary Outcome Measures

  1. Sensitivity of the test (10 microRNA) [24 months]

    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.

  2. Specificity of the test (10 microRNA) [24 months]

    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.

  3. Positive predictive value (PPV) of the test (10 microRNA) [24 months]

    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).

  4. Negative predictive value (NPV) of the test (10 microRNA) [24 months]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Man or woman whose Age is ≥ 18 years

  2. Patient requiring ultrasound for thyroid nodule scanning with established indication of FNAC

  3. Patient with Bethesda 3, 4 and 5 thyroid nodule

  4. Informed patient and signed informed consent received

  5. Patient affiliated to a French medical coverage system

Exclusion Criteria:
  1. Patient under guardianship, curatorship or safeguarding of justice

  2. Patient whose medical or psychological conditions do not permit them to complete the study or to sign the consent,

  3. Patient with metastatic cancer distinct from thyroid cancer

  4. Patient who has stopped treatment (chemotherapy / immunotherapy) for cancer for less than 6 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU de Toulouse Toulouse Haute-Garonne France 31000
2 Institut régional du Cancer de Montpellier Montpellier Hérault France 34298

Sponsors and Collaborators

  • Institut du Cancer de Montpellier - Val d'Aurelle

Investigators

  • Study Chair: Christine Rivière, MD, Institut régional du Cancer de Montpellier

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Institut du Cancer de Montpellier - Val d'Aurelle
ClinicalTrials.gov Identifier:
NCT04285476
Other Study ID Numbers:
  • PROCIM 2020-02 PRE
First Posted:
Feb 26, 2020
Last Update Posted:
Aug 3, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 3, 2022