AMH Dynamic Changes to Predict Ovarian Reserve in Perimenopausal Breast Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age45-55
SponsorShengjing Hospital

About this trial

This study is a prospective observational cohort study aimed at developing a clinical model based on dynamic changes in anti-Müllerian hormone (AMH) to predict ovarian reserve in perimenopausal women with hormone receptor-positive breast cancer.

The study will enroll approximately 300 women aged 45-55 years with perimenopausal status confirmed by menstrual history and hormone levels (FSH 10-40 IU/L, E2 \>20 pg/mL). Participants will be stratified by treatment regimen: (A) chemotherapy plus endocrine therapy, (B) chemotherapy plus targeted therapy plus endocrine therapy, and (C) endocrine therapy alone.

Blood samples will be collected at seven time points to measure AMH, FSH, E2, and LH. Menstrual patterns and menopausal symptoms will be recorded prospectively. The primary outcome is the association between dynamic AMH changes and the occurrence of menopause. A predictive model will be constructed using LASSO regression and Cox proportional hazards models, with internal validation by bootstrap resampling.

The goal is to develop a clinically applicable tool to guide endocrine therapy decisions-including the duration of ovarian function suppression (OFS), choice between tamoxifen and aromatase inhibitors (AIs), and selection of CDK4/6 inhibitors-as well as to provide individualized fertility preservation counseling for perimenopausal breast cancer patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female, aged 45-55 years

Histologically confirmed hormone receptor-positive breast cancer

Perimenopausal status defined as: (a) last menstrual period within 3 months prior to enrollment; and (b) FSH 10-40 IU/L and E2 >20 pg/mL

Scheduled to receive adjuvant chemotherapy and/or endocrine therapy

Disqualifiers

Postmenopausal status

Prior bilateral oophorectomy or pelvic radiotherapy

Severe hepatic or renal dysfunction

Estrogen receptor (ER)-negative and progesterone receptor (PR)-negative breast cancer

Trial population

This study will enroll approximately 300 perimenopausal women aged 45-55 years with histologically confirmed hormone receptor-positive breast cancer treated at Liaoning Cancer Hospital. Participants will be stratified into three groups based on treatment regimen: chemotherapy plus endocrine therapy (Group A), chemotherapy plus targeted therapy plus endocrine therapy (Group B), and endocrine therapy alone (Group C). All participants must meet perimenopausal status criteria defined by menstrual history and hormone levels (FSH 10-40 IU/L, E2 \>20 pg/mL) at enrollment.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

300 Participants
are grouped into 3 trial groups
Group A: Group A
Group B: Group B
Group C: Group C

Trial outcomes

Primary outcomes

1

Association Between Dynamic AMH Changes and Occurrence of Menopause

The primary outcome is the association between serial changes in anti-Müllerian hormone (AMH) levels measured at seven time points and the occurrence of menopause, defined as 12 consecutive months of amenorrhea in the absence of other causes.

Time frame
Up to 36 months

Secondary outcomes

1

Resumption of Menstrual Bleeding After Treatment

Proportion of participants who resume menstrual bleeding following chemotherapy or endocrine therapy.

Time frame
Up to 36 months
2

Changes in FSH, E2, and LH Levels

Serial changes in follicle-stimulating hormone (FSH), estradiol (E2), and luteinizing hormone (LH) levels over time.

Time frame
Up to 36 months
3

Menopausal Symptom Score

Changes in menopausal symptom severity assessed using a validated menopausal symptom rating scale.

Time frame
Up to 36 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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Shengjing Hospital

Lead sponsor

Liaoning Cancer Hospital & Institute

Sponsor institution

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