Skip to content

the exploration of short-term menupause prediction by AMH to optimize adjuvant endocrine therapy in peri-menupausal Lunimal/HER2- breast cancer patients

the exploration of short-term menupause prediction by AMH to optimize adjuvant endocrine therapy in peri-menupausal Lunimal/HER2- breast cancer patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073380
Enrollment
Unknown
Registered
2023-07-10
Start date
2023-07-10
Completion date
Unknown
Last updated
2023-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer

Interventions

Group of breast cancer (switch to AI for endocrine treatment):None

Sponsors

Obstetrics and Gynecology Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. female, premenopausal, aged 45-55 years; pre-menopausal before treatment 2. pathological confirmed invasive breast cancer, TNM stage:T1-2N0-1M0; 3. IHC confirmed ER>50% + and FISH confirmed HER2; 4. undergoing mastectomy or breast conserving surgery, SLNB or ALND; 5. AMH<0.1ng/ml before systemic therapy 6. normal blood routine 7. normal liver and renal function; 8. ECOG 1-2; 9. breast US, MRI, CT, etc for all cases; 10. not pregnant during treatment and hCG - before treatment; 11. well cooperated and informed consented.

Exclusion criteria

Exclusion criteria: 1) distant metastasis at diagnosis; 2) receiving neoadjuvant treatment; 3) Dexamethasone allergy or other serious allergy; 4) serious cardiovascular, pulmonary, liver, renal, nervous, or psychiatry disease; 5) nerve disease NCI=1grade 6) refuse treatment, mental disease 7) pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Estradiol;menstruation;anti-Mullerian hormone, AMH;

Countries

China

Contacts

Public ContactChen Hongliang

Obstetrics and Gynecology Hospital of Fudan University

13671852284@163.com+86 136 7185 2284

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026