Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05333328
Other study ID # 2021-1151-002
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date February 6, 2023
Est. completion date January 2033

Study information

Verified date December 2022
Source Gangnam Severance Hospital
Contact Sung Gwe Ahn, M.D.,Ph.D.
Phone 0220193370
Email asg2004@yuhs.ac
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Among ER+HER2- premenopausal patients with N1 who undergoes primary breast surgery, we will identify the patients with a genomic low risk using the multigene-assay (OncoFREE®). In these, ovarian function suppression with endocrine therapies including either tamoxifen or aromatase-inhibitors will be administered for 5 years.


Description:

- Among ER+HER2- premenopausal patients with N1 who undergoes primary breast surgery, we will identify the patients with a genomic low risk using the multigene-assay (OncoFREE®). - In these, ovarian function suppression (OFS) with endocrine therapies including either tamoxifen or aromatase-inhibitors will be administered for 5 years. - Either goserelin acetate or leuprorelin Acetate is allowed. - These patients are able to choose bilateral salpingo-oophorectomy instead of OFS. - Chemotherapy is omitted in these patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 418
Est. completion date January 2033
Est. primary completion date January 2028
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - ER+HER2- breast cancer - Premenopausal and age <=50 - T1 or T2 - N1 including micrometastasis - Genomic Low Risk by OncoFREE test® (1-20) Exclusion Criteria: - Postmenopausal women - ER-negative breast cancer

Study Design


Intervention

Drug:
Ovarian function suppression with endocrine treatments
Ovarian function suppression (OFS) with endocrine therapies including either tamoxifen or aromatase-inhibitors will be administered for 5 years. Either goserelin acetate or leuprorelin Acetate is allowed. These patients are able to choose bilateral salpingo-oophorectomy instead of OFS. Chemotherapy is omitted in these patients.

Locations

Country Name City State
Korea, Republic of Gangnam Severance Hospital Seoul Korea
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
Gangnam Severance Hospital Seoul National University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Distant recurrence-free survival The interval between the date of primary surgery and the date of last censored, or distant recurrence or death of any cause 5-years distant recurrence-free survival
Secondary Recurrence-free survival (RFS) The interval between the date of primary surgery and the date of last censored, or any type of recurrence or death of any cause 5-years RFS
Secondary Invasive disease-free survival (iDFS) The interval between the date of primary surgery and the date of last censored, or any type of invasive disease except thyroid cancer or death of any cause 5-years iDFS
See also
  Status Clinical Trial Phase
Recruiting NCT04681911 - Inetetamab Combined With Pyrotinib and Chemotherapy in the Treatment of HER2 Positive Metastatic Breast Cancer Phase 2
Completed NCT04890327 - Web-based Family History Tool N/A
Terminated NCT04066790 - Pyrotinib or Trastuzumab Plus Nab-paclitaxel as Neoadjuvant Therapy in HER2-positive Breast Cancer Phase 2
Completed NCT03591848 - Pilot Study of a Web-based Decision Aid for Young Women With Breast Cancer, During the Proposal for Preservation of Fertility N/A
Recruiting NCT03954197 - Evaluation of Priming Before in Vitro Maturation for Fertility Preservation in Breast Cancer Patients N/A
Terminated NCT02202746 - A Study to Assess the Safety and Efficacy of the VEGFR-FGFR-PDGFR Inhibitor, Lucitanib, Given to Patients With Metastatic Breast Cancer Phase 2
Active, not recruiting NCT01472094 - The Hurria Older PatiEnts (HOPE) With Breast Cancer Study
Completed NCT06049446 - Combining CEM and Magnetic Seed Localization of Non-Palpable Breast Tumors
Withdrawn NCT06057636 - Hypnosis for Pain in Black Women With Advanced Breast Cancer: A Feasibility Study N/A
Recruiting NCT05560334 - A Single-Arm, Open, Exploratory Clinical Study of Pemigatinib in the Treatment of HER2-negative Advanced Breast Cancer Patients With FGFR Alterations Phase 2
Active, not recruiting NCT05501769 - ARV-471 in Combination With Everolimus for the Treatment of Advanced or Metastatic ER+, HER2- Breast Cancer Phase 1
Recruiting NCT04631835 - Phase I Study of the HS-10352 in Patients With Advanced Breast Cancer Phase 1
Completed NCT04307407 - Exercise in Breast Cancer Survivors N/A
Recruiting NCT03544762 - Correlation of 16α-[18F]Fluoro-17β-estradiol PET Imaging With ESR1 Mutation Phase 3
Terminated NCT02482389 - Study of Preoperative Boost Radiotherapy N/A
Enrolling by invitation NCT00068003 - Harvesting Cells for Experimental Cancer Treatments
Completed NCT00226967 - Stress, Diurnal Cortisol, and Breast Cancer Survival
Recruiting NCT06006390 - CEA Targeting Chimeric Antigen Receptor T Lymphocytes (CAR-T) in the Treatment of CEA Positive Advanced Solid Tumors Phase 1/Phase 2
Recruiting NCT06037954 - A Study of Mental Health Care in People With Cancer N/A
Recruiting NCT06019325 - Rhomboid Intercostal Plane Block on Chronic Pain Incidence and Acute Pain Scores After Mastectomy N/A