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Density Lowering Effect of OFS Add on to TMX(DELFINO Trial)

Density Lowering Effect of Ovarian Function Suppression in Premenopausal Breast Cancer Patients Who Had no Density Change With One Year of Tamoxifen Treatment

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03664895
Enrollment
224
Registered
2018-09-11
Start date
2018-09-03
Completion date
2024-12-31
Last updated
2023-12-04

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

Conditions

Breast Cancer Invasive

Keywords

premenopausal women, MMG density, Ovary function suppression

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) 1. 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) 2. Check MMG Density via Volpara After 1yr TMX (At1yrMD) Check menopausal status after 1yr TMX(Menstruation episode or FSH \<30) 3. MMG Density Reduction(MDR =BaMD-AtMD ) at 1yr 4. MDR ≥5% -\> Keep go on TMX MDR \<5% -\> 1:1 randomization -\> Keep go on TMX vs OFS add on to TMX 5. Analysis : 5yr MDR (1'endpoint), 5yr DFS(2'endpoint), 5yr OS 6. 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

Interventions

DRUGLeuplin or zoladex

OFS(Leuplin or zoladex) add on to TMX

Sponsors

Seoul National University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
MMG density Reduction5 years

Secondary

MeasureTime frame
Disease free survival5 years

Other

MeasureTime frame
overall survival5 years

Countries

South Korea

Contacts

Primary ContactEun-Shin Lee
silvershoe99@gmail.com82-2-2072-0173

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026