Density Lowering Effect of "OFS Add on to TMX"(DELFINO Trial)
Primary Purpose
Breast Cancer Invasive
Status
Recruiting
Phase
Phase 3
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Leuplin or zoladex
Sponsored by
About this trial
This is an interventional treatment trial for Breast Cancer Invasive focused on measuring premenopausal women, MMG density, Ovary function suppression
Eligibility Criteria
Inclusion Criteria:
- Premenopausal women, ER+ breast cancer, stage I~III, underwent standard treatment including surgery, Planned TMX
- available MMG density check via Volpara
Exclusion Criteria:
- Bilateral breast cancer
- Prior endocrine therapy
- Postmenopausal status
- unavailable MMG density check via volpara before and after TMX
Sites / Locations
- Seoul National University HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
No Intervention
Active Comparator
Arm Label
observation arm(TMX, MDR≥5%)
control arm(TMX, MDR<5%)
OFS add arm(TMX + OFS, MDR<5%)
Arm Description
keep go on TMX
keep go on TMX
OFS add on to TMX
Outcomes
Primary Outcome Measures
MMG density Reduction
Secondary Outcome Measures
Disease free survival
Full Information
NCT ID
NCT03664895
First Posted
September 7, 2018
Last Updated
October 16, 2022
Sponsor
Seoul National University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03664895
Brief Title
Density Lowering Effect of "OFS Add on to TMX"(DELFINO Trial)
Official Title
Density Lowering Effect of Ovarian Function Suppression in Premenopausal Breast Cancer Patients Who Had no Density Change With One Year of Tamoxifen Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 3, 2018 (Actual)
Primary Completion Date
September 2, 2023 (Anticipated)
Study Completion Date
October 2, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Seoul National University Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
DELFINO tial is designed to investigate the role of "OFS add on to TMX ", based on MMG density as a surrogate marker in premenopausal women
Premise - MMG density as a surrogate marker of hormone therapy
Assumption - "Add on OFS to TMX" would have further decrease of density
3-arm(Observation arm + Randomised 2-arm), phase III, RCT with 1:1 allocation
Detailed Description
Enroll : Sep03,2018~(Planned N= 224)
Inclusion criteria
Premenopausal
ER+
Planned tamoxifen(TMX)
No planned ovary function suppression(OFS)
Regardless of ChemoTx
Mammography(MMG) density check via Volpara*(=Baseline MMG density, BaMD) (*Volpara= software to check MMG density)
Check MMG Density via Volpara After 1yr TMX (At1yrMD) Check menopausal status after 1yr TMX(Menstruation episode or FSH <30)
MMG Density Reduction(MDR =BaMD-AtMD ) at 1yr
MDR ≥5% -> Keep go on TMX MDR <5% -> 1:1 randomization -> Keep go on TMX vs OFS add on to TMX
Analysis : 5yr MDR (1'endpoint), 5yr DFS(2'endpoint), 5yr OS
Calculation of patients' number In previous study(<Kim et al. Breast Can Res 2012>) MDR (Mammography Density Reduction) was found in about 50% of all patients who received endocrine therapy.
Expected
MDR in "TMX only" cohort -> 6 ± 7%
MDR in "OFS add on to TMX" -> 10 ± 7%
after 1yr, Significance level 5%, average MDR 4% difference, 80% power, 10% dropout rate => 1:1 randomization Number = 112(56:56) Total number = 224
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Invasive
Keywords
premenopausal women, MMG density, Ovary function suppression
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
224 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
observation arm(TMX, MDR≥5%)
Arm Type
No Intervention
Arm Description
keep go on TMX
Arm Title
control arm(TMX, MDR<5%)
Arm Type
No Intervention
Arm Description
keep go on TMX
Arm Title
OFS add arm(TMX + OFS, MDR<5%)
Arm Type
Active Comparator
Arm Description
OFS add on to TMX
Intervention Type
Drug
Intervention Name(s)
Leuplin or zoladex
Intervention Description
OFS(Leuplin or zoladex) add on to TMX
Primary Outcome Measure Information:
Title
MMG density Reduction
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Disease free survival
Time Frame
5 years
Other Pre-specified Outcome Measures:
Title
overall survival
Time Frame
5 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Premenopausal women, ER+ breast cancer, stage I~III, underwent standard treatment including surgery, Planned TMX
available MMG density check via Volpara
Exclusion Criteria:
Bilateral breast cancer
Prior endocrine therapy
Postmenopausal status
unavailable MMG density check via volpara before and after TMX
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eun-Shin Lee
Phone
82-2-2072-0173
Email
silvershoe99@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wonshik Han
Organizational Affiliation
Seoul National University College of Medicine/Seoul National University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
ZIP/Postal Code
110-744
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wonshik Han, MD PhD
Phone
82-2-2072-1958
Email
hanw@snu.ac.kr
First Name & Middle Initial & Last Name & Degree
Eun-Shin Lee, MD
Email
silvershoe99@gmail.com
First Name & Middle Initial & Last Name & Degree
Eun-Shin Lee, MD
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Density Lowering Effect of "OFS Add on to TMX"(DELFINO Trial)
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