Evaluation of Metformin Effect on the Fertility of Women Treated With 131I for Thyroid Cancer (METHYR)
Primary Purpose
Thyroid Cancer
Status
Not yet recruiting
Phase
Phase 3
Locations
Poland
Study Type
Interventional
Intervention
metformin
Radioactive iodine (I-131)
Sponsored by
About this trial
This is an interventional treatment trial for Thyroid Cancer
Eligibility Criteria
Inclusion Criteria:
- Female subjects in reproductive age >18 <45.
- Subjects with diagnosed papillary thyroid carcinoma with various pathological, stage TNM (I-II).
- Subjects not treated with 131I.
- Serum TSH concentration 0.1-4.9 mU/l.
- Willingness to comply with protocol procedures.
Exclusion Criteria:
- Hypersensitivity to metformin.
- Subjects with polycystic ovarian syndrome or other diseases of the ovaries (primary / secondary ovarian failure).
- Subjects taking metformin during last week.
- Subjects with liver malfunction and abnormal hepatitis marker results (ALT and AST activity >3ULN.
- Subjects with eGFR below 45ml/min/1.73m2.
- Subjects with lactic acidosis or having history of metabolic acidosis.
- Subjects with serum AMH concentration below lower range norm.
- Subjects with history of congestive heart disease NYHA stage III/IV.
- Subjects with acute myocardial ischemia (CCS 3-4).
- Subjects with history of sepsis or severe infection.
- Subject with lung disease (uncontrolled asthma based on GINA 2000 Guidelines and COPD GOLD ≥ 3 stage).
- Positive result of pregnancy test or pregnancy planned during the study.
- Alcohol or other substance dependent syndromes.
- BMI <18.5 kg/m2.
- Accompanying diseases with poor prognosis in the opinion of the researcher.
- As per Investigator (or his designee) judgement, subject cannot participate in the study due to reasons (i.e. medical, psychiatric and/or social reason).
- Unreliability or lack of cooperation.
Sites / Locations
- Department of Endocrinology, Diabetology and Internal Medicine, Medical Univeristy of Bialystok
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
No Intervention
Arm Label
Metformin
Placebo
Observational
Arm Description
patients qualified to receive metformin and 131I treatment
patients receiving placebo and 131 I treatment
observation group, patients after thyroidectomy, characterized by low risk of cancer progression, in this case, not qualified for 131I treatment
Outcomes
Primary Outcome Measures
Changes in AMH, Inhibin B and FSH levels due to the action of metformin
The primary endpoint will be to evaluate the effect of metformin on the difference in serum AMH, inhibin B and FSH concentration and the number of antral follicles, assessed in the study groups consisted of the women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
Secondary Outcome Measures
Assessment of the effect of metformin on the parameters of oxidative stress
To evaluate the metformin modulating impact on the concentrations of selected parameters of oxidative stress assessed in the study groups consisted of the women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
The evaluate of difference in serum concentration of selected parameters of apoptosis
To evaluate the effect of metformin on the difference in serum concentration of selected parameters of apoptosis between the study groups in women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
The evaluate of difference in expression in selected microRNA
To evaluate the effect of metformin on the difference of expression in selected microRNA between the study groups in women with papillary thyroid cancer, treated with 131I, between the randomized visit and V3, V4, V5 and V6 visit
Full Information
NCT ID
NCT05468554
First Posted
July 8, 2022
Last Updated
October 17, 2022
Sponsor
Medical University of Bialystok
Collaborators
Medical Research Agency, Poland
1. Study Identification
Unique Protocol Identification Number
NCT05468554
Brief Title
Evaluation of Metformin Effect on the Fertility of Women Treated With 131I for Thyroid Cancer
Acronym
METHYR
Official Title
Evaluation of Metformin Effect on the Fertility of Women Treated With 131I for Thyroid Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 1, 2022 (Anticipated)
Primary Completion Date
April 30, 2026 (Anticipated)
Study Completion Date
April 30, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Bialystok
Collaborators
Medical Research Agency, Poland
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study is aimed to investigate the metformin effect on the fertility of women treated with 131 I for thyroid cancer
Detailed Description
One of the most common types of endocrine cancer, especially in young women, is thyroid cancer. More than 90% of all thyroid cancers are differentiated thyroid cancers (DTC), including papillary thyroid cancer (PTC) and follicular cancer. Papillary thyroid cancer is considered as indolent tumour as progression free survival is 10 years of 98%. As per current knowledge and basing on current literature most of the PTC are considered to be low incidence of recurrence or metastasis, however, there are more invasive/aggressive types with very specific pathological and molecular characteristics. The aggressive variants of PTC were strictly associated with higher rates of extrathyroid extension, multifocality, and nodal and distant metastasis. Thyroidectomy followed by radioactive iodine 131 (131I) therapy, in higher stages of PTC disease to ablate residual thyroid cancer or treat metastases, significantly increase survival Metformin (1,1-dimethylbiguanide) is an oral antihyperglycemic drug. Orally administered metformin is absorbed into the blood in 40-60% of the drug dose. Maximum blood levels are reached after approximately 2.5 hours for the immediate-release formulation and 7 hours for the prolonged-release tablets. It is not metabolised in the liver, however, it is excreted unchanged by the kidneys, mainly through the renal tubules. Metformin is used in patients with type 2 diabetes and prediabetes as well as in insulin resistant state and in women with polycystic ovary syndrome (PCOS). Metformin works by lowering level of glucose in the blood by lowering its production by the liver and increasing the sensitivity to insulin by muscle and fat tissue. It also has a beneficial effect on serum lipids by reducing the concentration of triglycerides, total cholesterol, LDL-cholesterol and VLDL. Additionally, this drug has also several other biological effects such as anti-inflammatory, anticancer, hepatoprotective, cardioprotective, otoprotective, radioprotective and radio-sensitising.
Currently there is also a large evidential material for effectiveness of metformin therapy in re-establishing of reproductive functions and fertility in women with polycystic ovary syndrome.
Having proved the metformin restore of ovulation in PCOS and has antioxidant properties there are indications that metformin can be a therapy which will helps to maintain ovary follicle number on acceptable level. At present, there are no performed studies concerned on the evaluation of the potential beneficial effect of metformin application impact on fertility parameters in the group of women treated with 131I. Therefore, the proposed study will assess the effect of metformin intervention on the indirect parameters of fertility of women treated with 131I for papillary thyroid cancer
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
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Arm A - patients qualified to receive metformin and 131I treatment, arm B - patients receiving placebo and 131 I treatment. Arm C- observation group, patients undergoing thyroidectomy, characterized by low risk of disease progression, in this case, not qualified for the 131I treatment.
Masking
ParticipantCare ProviderInvestigator
Masking Description
double blind / placebo controlled
Allocation
Randomized
Enrollment
160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Metformin
Arm Type
Experimental
Arm Description
patients qualified to receive metformin and 131I treatment
Arm Title
Placebo
Arm Type
Active Comparator
Arm Description
patients receiving placebo and 131 I treatment
Arm Title
Observational
Arm Type
No Intervention
Arm Description
observation group, patients after thyroidectomy, characterized by low risk of cancer progression, in this case, not qualified for 131I treatment
Intervention Type
Drug
Intervention Name(s)
metformin
Intervention Description
Metformin will be used 3 times a day (3x500mg), starting in the first week with 1x1 tablet (1x500 mg for breakfast), in the second week, 2x1 tablet (500 mg for breakfast and 500 mg for dinner), from the 3rd week 3x1 tablet. (3x500mg with main meals). A gradual escalation of the dose is planned to the point of developing drug intolerance or toxicity that is unacceptable to the patient.
Intervention Type
Radiation
Intervention Name(s)
Radioactive iodine (I-131)
Intervention Description
Patients qualified to receive 131I treatment
Primary Outcome Measure Information:
Title
Changes in AMH, Inhibin B and FSH levels due to the action of metformin
Description
The primary endpoint will be to evaluate the effect of metformin on the difference in serum AMH, inhibin B and FSH concentration and the number of antral follicles, assessed in the study groups consisted of the women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
Time Frame
4 years
Secondary Outcome Measure Information:
Title
Assessment of the effect of metformin on the parameters of oxidative stress
Description
To evaluate the metformin modulating impact on the concentrations of selected parameters of oxidative stress assessed in the study groups consisted of the women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
Time Frame
4 years
Title
The evaluate of difference in serum concentration of selected parameters of apoptosis
Description
To evaluate the effect of metformin on the difference in serum concentration of selected parameters of apoptosis between the study groups in women with papillary thyroid cancer, treated with 131I, comparing received results during the randomized, V3, V4, V5 and V6 visits
Time Frame
4 years
Title
The evaluate of difference in expression in selected microRNA
Description
To evaluate the effect of metformin on the difference of expression in selected microRNA between the study groups in women with papillary thyroid cancer, treated with 131I, between the randomized visit and V3, V4, V5 and V6 visit
Time Frame
4 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Female subjects in reproductive age >18 <45.
Subjects with diagnosed papillary thyroid carcinoma with various pathological, stage TNM (I-II).
Subjects not treated with 131I.
Serum TSH concentration 0.1-4.9 mU/l.
Willingness to comply with protocol procedures.
Exclusion Criteria:
Hypersensitivity to metformin.
Subjects with polycystic ovarian syndrome or other diseases of the ovaries (primary / secondary ovarian failure).
Subjects taking metformin during last week.
Subjects with liver malfunction and abnormal hepatitis marker results (ALT and AST activity >3ULN.
Subjects with eGFR below 45ml/min/1.73m2.
Subjects with lactic acidosis or having history of metabolic acidosis.
Subjects with serum AMH concentration below lower range norm.
Subjects with history of congestive heart disease NYHA stage III/IV.
Subjects with acute myocardial ischemia (CCS 3-4).
Subjects with history of sepsis or severe infection.
Subject with lung disease (uncontrolled asthma based on GINA 2000 Guidelines and COPD GOLD ≥ 3 stage).
Positive result of pregnancy test or pregnancy planned during the study.
Alcohol or other substance dependent syndromes.
BMI <18.5 kg/m2.
Accompanying diseases with poor prognosis in the opinion of the researcher.
As per Investigator (or his designee) judgement, subject cannot participate in the study due to reasons (i.e. medical, psychiatric and/or social reason).
Unreliability or lack of cooperation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Agnieszka Adamska, Assoc.Prof.
Phone
+48 85 746 86 07
Email
methyr@umb.edu.pl, agnieszka.adamska@umb.edu.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Aldona Kowalska, Assoc.Prof.
Phone
+48 41 36 74 181
Email
aldona.kowalska@onkol.kielce.pl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agnieszka Adamska, Assoc.Prof.
Organizational Affiliation
Medical University of Bialystok
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Endocrinology, Diabetology and Internal Medicine, Medical Univeristy of Bialystok
City
Bialystok
ZIP/Postal Code
15-276
Country
Poland
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Metformin Effect on the Fertility of Women Treated With 131I for Thyroid Cancer
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