Endocrine Therapy Base on 21-gene RS

NCT ID: NCT07311122

Last Updated: 2025-12-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

4000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2026-01-01

Study Completion Date

2028-12-31

Brief Summary

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Among patients aged ≤50 years with hormone receptor-positive, HER2-negative breast cancer and pathologic nodal stage pN0-1-limited to those with an Oncotype DX® Recurrence Score (RS) of 11-25 for pN0 and ≤25 for pN1-, we will investigate the followings:

i) Real-world patterns of adjuvant therapy (systemic chemotherapy and endocrine therapy) and radiotherapy according to N stage and Oncotype DX® RS.

ii) Clinicopathologic characteristics of each patient subgroup by adjuvant treatment modality and RS category.

iii) Survival outcomes and independent prognostic factors according to RS. iv) Survival analyses by adjuvant treatment modality, stratified by RS category, clinical risk, and N stage.

Through these analyses, we aim to establish clinical evidence on whether endocrine therapy combined with ovarian function suppression (OFS) can substitute for adjuvant chemotherapy in HR+/HER2- patients with pN0-1 disease within the above RS ranges, and-if so-to define the patient subsets for whom this substitution is appropriate.

Detailed Description

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Conditions

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Breast Cancer

Keywords

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Breast cancer Hormone receptor-positive Oncotype DX Chemotherapy Ovarian function suppression

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Oncotype DX

All patients received Oncotype DX test.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

1. Histologically confirmed breast cancer.
2. Age ≤50 years at initial diagnosis.
3. Premenopausal at diagnosis, defined as any of the following:

A. History of menstruation within 6 months prior to diagnosis. B. Serum FSH \< 30 mIU/mL. C. If criteria A or B are unavailable, women aged ≤50 years are considered premenopausal.
4. Underwent curative-intent breast cancer surgery between January 2012 and December 2021.
5. Pathologic tumor stage pT1-pT3 after surgery.
6. Pathologic nodal stage pN0-pN1 after surgery.
7. Hormone receptor-positive disease by immunohistochemistry (IHC): estrogen receptor (ER) and/or progesterone receptor (PR) positive (≥1% positive cells or Allred score ≥3).
8. HER2-negative disease per ASCO/CAP guidelines: IHC 0 or 1+; if IHC 2+, in situ hybridization (FISH or SISH) negative.
9. Oncotype DX® performed, meeting one of the following Recurrence Score (RS) ranges:

A. pN0: RS 11-25. B. pN1: RS ≤25.

Exclusion Criteria

1. Evidence of distant (systemic) metastasis at diagnosis.
2. Postmenopausal status at diagnosis, defined as any of the following:

A. Prior bilateral oophorectomy before the breast cancer diagnosis (considered postmenopausal).

B. Prior unilateral oophorectomy alone is not considered postmenopausal (classified as premenopausal).

C. Bilateral oophorectomy performed after breast cancer surgery for therapeutic purposes is not an exclusion; such patients will be categorized as having received ovarian function suppression (OFS).

D. Serum FSH ≥ 30 mIU/mL.
3. Hormone receptor-negative or HER2-positive disease.
4. Insufficient or unclear data regarding the type of adjuvant therapy received.
5. History of another malignancy treated before the breast cancer diagnosis, except for thyroid cancer and non-melanoma skin cancer.
6. Bilateral breast cancer.
7. Receipt of neoadjuvant systemic therapy prior to surgery.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Gangnam Severance Hospital

OTHER

Sponsor Role lead

Responsible Party

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Soong June Bae

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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KBCSG 38

Identifier Type: -

Identifier Source: org_study_id