AzTrials
AzTrials

Hormone Receptor-positive Breast CancerNCT04891731

Efficacy and Safety of Leuprorelin 3M in Premenopausal Women With Hormone Receptor-positive Breast Cancer

An observational study of Hormone Receptor-positive Breast Cancer, run by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

Leuprorelin, a LHRH agonist, acts as a potent inhibitor of gonadotropin secretion and is commonly used for the treatment of hormone-responsive prostate cancer, premenopausal HR+ breast cancer, endometriosis and uterine fibroids. It is currently available in 1M, 3M, 6M for subcutaneous administration. Read more about this study

Who is it for?
Ages 18 years and older, women onlyHealthy volunteers can take part
Conditions the study is for
Hormone Receptor-positive Breast Cancer
What is being tested?
AI or TAM
Type of treatment
Injection or infusion
How many people
120 participants
Where
No sites listed yet
Study dates
May 2021to Sep 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Women only
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Premenopausal patients with histologically confirmed hormone receptor-positive breast cancer

Who may be able to join

  • age≥18 years;
  • Tumor that expressed ER or progesterone receptor in at least 10% of the cells, as assessed by immunohistochemical testing
  • T1 to T3, any N, and M0, according to the TNM classification
  • Any type of breast surgical procedure
  • Any type of preoperative and/or postoperative adjuvant chemotherapy prior to enrollment
  • Capable of receiving the study drug within 12 weeks after surgery or after postoperative chemotherapy completion prior to enrollment
  • Eastern Cooperative Oncology Group performance status of Grade 0 or 1

Who cannot join

  • Bilateral oophorectomy or ovarian irradiation
  • No use of other OFS drugs

Trial locations and contacts

No sites are listed yet.

Jingna Lin, MD contact

18819430558

229320178@qq.com

Yudong Li, MD contact

020-34071156

910870698@qq.com

About this study

Official title: Efficacy and Safety of Leuprorelin Acetate Every-3-months Depot Plus an Aromatase Inhibitor or Tamoxifen in Premenopausal Women With Hormone Receptor-positive Breast Cancer: a Clinical Prospective Observational Study

Leuprorelin, a LHRH agonist, acts as a potent inhibitor of gonadotropin secretion and is commonly used for the treatment of hormone-responsive prostate cancer, premenopausal HR+ breast cancer, endometriosis and uterine fibroids. It is currently available in 1M, 3M, 6M for subcutaneous administration. Initially administration would stimulate an increase in LH and FSH, causing a transient increase of E2 in 2-4 weeks. Continuous administration results in a subsequent decrease in E2 levels, as a result of decreased levels of luteinizing LH and FSH. After stopping injection, ovarian function could gradually recover. Adverse events related to leuprorelin include flushing, mood swings and urogenital symptoms.

At present, the treatment of premenopausal breast cancer mainly includes 1M and 3M GnRHa. Leuprorelin 11.25mg dosage form is currently the only 3M GnRHa in China that has gotten breast cancer indications. The use of 3M GnRHa could improve patients' compliance and reduce injection discomfort. However, previous studies about GnRHa alone or in combination with TAM or AIs usually used 1M GnRHa. There have been few studies reporting the suppression effects of E2 levels and clinical outcome with leuprorelin 3M in combination with TAM or AIs.

Read the detailed description

Background:

There are some differences in the age of onset of breast cancer, histopathological types, and treatment methods between Asians and non-Asians. Incidence peaks at age 40-50 in Asian women, with more than half of premenopausal patients, but 65-70 years in US women, most of which are postmenopausal[1]. Besides, compared with Americans, Asian women younger than 50 have a higher prevalence of luminal A breast cancer and less basal-like subtype. Therefore, the application of OFS has always been the focus for the treatment of premenopausal women with HR+ breast cancer in Asia.

OFS therapy includes oophorectomy, ovarian radiation, and the use of GnRHa. Several studies have shown that the use of GnRHa in premenopausal women can achieve similar efficacy to oophorectomy and ovarian radiation therapy. As GnRHa has the advantages of non-invasiveness and reversibility, it has gradually replaced oophorectomy and ovarian radiation, and has become the main method of OFS in premenopausal women with HR+ breast cancer. Meanwhile, GnRHa in combination with TAM or AIs is increasingly used for premenopausal HR+ breast cancer patients. Previous studies have revealed that GnRHa alone or in combination with TAM or AIs has shown effective estrogen suppression and certain survival benefits for most patients with breast cancer. In addition, the 5-year follow-up results of the TEXT / SOFT study in 2014 showed that compared with OFS + TAM, OFS + AI treatment significantly improved DFS, prolonged cancer-free survival time and distant recurrence-free metastasis[8, 9]. The 9-year follow-up results of the TEXT / SOFT study in 2019 indicated that OFS + AI versus OFS + TAM or TAM single drugs, years of distant recurrence risk in patients with high risk of recurrence have an absolute benefit rate of 10-15 %, Intermediate risk is 4-5%, low-risk benefit is not obvious. In 2019, the ABCCG reviewed ESO-ESMO and St. Gallen's treatment recommendations for HR+/ Her-2 negative breast cancer in premenopausal women, discussed controversial issues and pointed out that patients with low recurrence risk can be treated with TAM alone. For patients with high risk of recurrence, chemotherapy + OFS + AI should be given. It indicates that not all premenopausal HR+ patients with early breast cancer need auxiliary OFS, and more clinical trials on OFSin premenopausal HR + patients are necessary and worthwhile.

Leuprorelin, a LHRH agonist, acts as a potent inhibitor of gonadotropin secretion and is commonly used for the treatment of hormone-responsive prostate cancer, premenopausal HR+ breast cancer, endometriosis and uterine fibroids. It is currently available in 1M, 3M, 6M for subcutaneous administration. Initially administration would stimulate an increase in LH and FSH, causing a transient increase of E2 in 2-4 weeks. Continuous administration results in a subsequent decrease in E2 levels, as a result of decreased levels of luteinizing LH and FSH. After stopping injection, ovarian function could gradually recover. Adverse events related to leuprorelin include flushing, mood swings and urogenital symptoms.

At present, the treatment of premenopausal breast cancer mainly includes 1M and 3M GnRHa. Leuprorelin 11.25mg dosage form is currently the only 3M GnRHa in China that has gotten breast cancer indications. The use of 3M GnRHa could improve patients' compliance and reduce injection discomfort. However, previous studies about GnRHa alone or in combination with TAM or AIs usually used 1M GnRHa. There have been few studies reporting the suppression effects of E2 levels and clinical outcome with leuprorelin 3M in combination with TAM or AIs.

To further investigate the suppression effects of E2 levels of 3M GnRHa, we conducted a single-arm, prospective clinical observational study evaluating the efficacy and safety of adjuvant therapy with leuprorelin 3M in combination with TAM or AIs in premenopausal HR+ breast cancer.

Being tested
AI or TAM

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • AI or TAMDrug

    This is an observational study, the researcher will describe the ratio of E2 control between leuprorelin plus TAM or leuprorelin plus AIs patients based on the actual clinical use.

Study groups in NCT04891731
Study groupRoleWhat they receive
leuprorelin 3M plus AIsleuprorelin 3M: 11.25 mg subcutaneous administration every 3 months for 1 year AIs: anastrozole 1mg /letrozole 2.5mg/exemestane 25mg daily for 1 year
Receives: Drug: AI or TAM
leuprorelin 3M plus TAMleuprorelin 3M: 11.25 mg subcutaneous administration every 3 months for 1 year TAM: daily for 1 year
Receives: Drug: AI or TAM

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. the suppression proportion of serum estradiol (E2)

    The suppression proportion of serum estradiol (E2) to the menopausal level (E2≤30 pg/mL) at different time points (4, 12, 24, 36 and 48 weeks) during the first year for leuprorelin 3M depot plus TAM or AIs.

    Measured: March,2023

Secondary outcomes (2)
  1. Quality of Life (QoL)

    To evaluate the Quality of Life (QoL) of Patient who receive Leu 3M depot for OFS treatment evaluated by FACT-B and FACT-ES questionnaire.

    Measured: March,2023

  2. Adverse events(AEs)

    To observe the incidence of adverse events(AEs).

    Measured: March,2023

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 May 2021
  2. Study startMay 2021 (estimated)
  3. Primary completionMay 2023 (estimated)
  4. Study completionSep 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04891731
Sponsor's protocol ID
SunYatsenU2H-LQ5
Status last verified
May 2021
First submitted
17 May 2021
Last updated
18 May 2021
Results posted
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Hormone Receptor-positive Breast Cancer, run by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 May 2021. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Jingna Lin, MD (18819430558, 229320178@qq.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

the suppression proportion of serum estradiol (E2) (time frame: March,2023). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 May 2021.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in