跳至主要内容
临床试验/NCT04891731
NCT04891731Unknown不适用

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

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University0 个研究点目标入组 120 人开始时间: 2021年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
120
主要终点
the suppression proportion of serum estradiol (E2)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 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

排除标准

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

研究组 & 干预措施

leuprorelin 3M plus AIs

leuprorelin 3M: 11.25 mg subcutaneous administration every 3 months for 1 year AIs: anastrozole 1mg /letrozole 2.5mg/exemestane 25mg daily for 1 year

干预措施: AI or TAM (Drug)

leuprorelin 3M plus TAM

leuprorelin 3M: 11.25 mg subcutaneous administration every 3 months for 1 year TAM: daily for 1 year

干预措施: AI or TAM (Drug)

结局指标

主要结局

the suppression proportion of serum estradiol (E2)

时间窗: March,2023

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.

次要结局

  • Quality of Life (QoL)(March,2023)
  • Adverse events(AEs)(March,2023)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Liu Qiang

Doctor

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

相似试验

撤回
4 期
Effect of Cetrorelex Acetate on Ovarian Function in Women Undergoing ChemotherapyOvarian FunctionPreservation of Ovarian Function
NCT00507780Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
进行中(未招募)
不适用
Efficacy and safety of a new Leuprolide acetate 3.75 mg depot formulation, GP-Pharm s.a., when given as palliative treatment to prostate cancer patients - Leuprolide 3.75 mgprostate cancer
EUCTR2005-002880-98-DEGP-Pharm s.a.160
进行中(未招募)
不适用
Efficacy and safety of a new Leuprolide acetate 3.75 mg depot formulation, GP-Pharm s.a., when given as palliative treatment to prostate cancer patients - Leuprolide 3.75 mgMedDRA version: 6.0Level: LLTClassification code 10007113prostate cancer
EUCTR2005-002880-98-HUGP-Pharm s.a.120
进行中(未招募)
不适用
Efficacy and safety of a new Leuprolide acetate 3.75 mg depot formulation, GP-Pharm s.a., when given as palliative treatment to prostate cancer patientsMedDRA version: 14.1Level: LLTClassification code 10007113Term: Cancer of prostateSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Prostate cancer
EUCTR2005-002880-98-ESGP-Pharm s.a120
进行中(未招募)
不适用
Efficacy and safety of a new Leuprolide acetate 3.75 mg depot formulation, GP-Pharm s.a., when given as palliative treatment to prostate cancer patients - Leuprolide 3.75 mgMedDRA version: 6.0Level: LLTClassification code 10007113prostate cancer
EUCTR2005-002880-98-ATGP-Pharm s.a.120