Neoadjuvant Endocrine Therapy for HR+/HER2- Breast Cancer
Evaluating the Response-Guided Therapy With Neoadjuvant Endocrine Therapy to Optimize Adjuvant Treatment in Premenopausal HR+/HER2- Breast Cancer (JCOG2402, Young HOPE)
Recruiting
Phase 3Interventional Study
Breast Cancer
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Pivotal Trial
This treatment is in the last trial phase before FDA approval.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Female
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
950 (estimated)
Sponsor
Tokyo Women's Medical University · Other
Who this trial is looking for
This trial is looking for premenopausal women with a specific type of breast cancer. Participants will receive treatment that may allow them to avoid chemotherapy if their cancer responds well to initial therapy.
Are You a Good Fit for This Trial?
You may be able to join if
I am a woman aged 18 or older
I have HR-positive/HER2-negative breast cancer
I have not had breast cancer before
I have no distant spread of my breast cancer
I am premenopausal and have had my period in the last 12 months
I show adequate organ function
I have ER expression of 10% or more
You may not be able to join if
I have another active cancer that needs treatment
I have an ongoing infection that requires treatment
I am pregnant, breastfeeding, or planning to become pregnant
I have a serious psychiatric condition affecting my daily life
I have unstable angina or a heart attack in the past 6 months
I have uncontrolled high blood pressure
I have uncontrolled diabetes despite treatment
I have interstitial pneumonia or severe lung disease
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Young HOPE/JCOG2402 is a multicenter, randomized phase III study designed to evaluate response-guided therapy following neoadjuvant endocrine therapy to optimize adjuvant treatment in premenopausal HR+/HER2- Breast Cancer.
Premenopausal women with intermediate-risk HR-positive/HER2-negative breast cancer derive benefit from the addition of chemotherapy to endocrine therapy. However, previous stud…
Young HOPE/JCOG2402 is a multicenter, randomized phase III study designed to evaluate response-guided therapy following neoadjuvant endocrine therapy to optimize adjuvant treatment in premenopausal HR+/HER2- Breast Cancer.
Premenopausal women with intermediate-risk HR-positive/HER2-negative breast cancer derive benefit from the addition of chemotherapy to endocrine therapy. However, previous studies have demonstrated that patients who achieve an endocrine response (Ki-67 ≤10%) following neoadjuvant endocrine therapy have excellent outcomes without chemotherapy, irrespective of menopausal status. These findings suggest that endocrine therapy response may serve as a predictive biomarker to identify premenopausal patients who can safely omit chemotherapy.
The primary objective of this study is to evaluate the non-inferiority of an ET response-guided treatment strategy compared with standard surgery followed by adjuvant therapy. The study aims to increase the proportion of patients who can be treated with endocrine therapy alone by omitting chemotherapy in those with highly endocrine-sensitive disease.
Eligible patients are randomized 1:1 to upfront surgery or neoadjuvant endocrine therapy with an aromatase inhibitor and ovarian function suppression. The primary endpoint is EFS. Secondary endpoints include overall survival, relapse-free survival, distant recurrrence-free survival, HR-QOL, the rate of endocrine therapy alone in adjuvant therapy, ET response rate in an Arm B, the rate of non-menopause and safety. A total of 950 patients will be enrolled. Randomization is stratified by cN0 vs cN1, HG1 or 2 vs 3, and institution.
The JCOG2402 trial addresses an unmet need in adjuvant therapy of premenopausal HR-positive, HER2-negative breast cancer with intermediate risk and may contribute to the establishment of a new treatment strategy.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Women aged 18 years or older
2. ECOG PS 0-1
3. HR-positive/HER2-negative breast cancer
4. ER expression ≥ 10%
5. cN0; HG 1: 3 cm\<T≤5 cm, HG 2: 2 cm\<T≤5 cm or HG3: 1 cm\<T≤5 cm cN1; cT\<5 cm and HG 1/HG 2
6. Premenopausal women with spontaneous menses within 12 months
7. No …
Inclusion Criteria:
1. Women aged 18 years or older
2. ECOG PS 0-1
3. HR-positive/HER2-negative breast cancer
4. ER expression ≥ 10%
5. cN0; HG 1: 3 cm\<T≤5 cm, HG 2: 2 cm\<T≤5 cm or HG3: 1 cm\<T≤5 cm cN1; cT\<5 cm and HG 1/HG 2
6. Premenopausal women with spontaneous menses within 12 months
7. No distant metastasis of breast cancer
8. No prior diagnosis of breast cancer.
9. No multiple regions of breast cancer
10. No contralateral breat cancer
11. Adequate organ function
Exclusion Criteria:
1. Presence of active double cancer (synchronous malignancy requiring treatment).
2. Ongoing infectious disease requiring systemic therapy. Fever ≥38.0°C at the time of registration.
3. Women who are pregnant, possibly pregnant, within 28 days postpartum, or breastfeeding; men whose partners intend to become pregnant.
4. Psychiatric illness or symptoms that interfere with daily living and may compromise trial participation.
5. Ongoing systemic administration (oral or IV) of steroids equivalent to ≥10 mg/day of prednisolone or other immunosuppressive agents.
6. Unstable angina (developed or worsened within the past 3 weeks) or myocardial infarction within the past 6 months.
7. Uncontrolled hypertension.
8. Uncontrolled diabetes mellitus despite continuous insulin or oral antidiabetic therapy.
9. Positive for HBs antigen or HCV antibodies (Patients positive for HCV antibodies are not excluded if HCV-RNA is undetectable.)
10. Positive for HIV antibodies (HIV testing is not mandatory.)
11. Presence of interstitial pneumonia, pulmonary fibrosis, or severe emphysema as diagnosed by chest CT.
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