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A Randomized Phase III Study of Response-Guided Therapy Following Neoadjuvant Endocrine Therapy to Optimize Adjuvant Treatment in Premenopausal HR+/HER2- Breast Cancer (JCOG2402, Young HOPE)

Status: Recruiting
Location: See all (49) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Women aged 18 years or older

• ECOG PS 0-1

• HR-positive/HER2-negative breast cancer

• ER expression ≥ 10%

• 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

• Premenopausal women with spontaneous menses within 12 months

• No distant metastasis of breast cancer

• No prior diagnosis of breast cancer.

• No multiple regions of breast cancer

⁃ No contralateral breat cancer

⁃ Adequate organ function

Locations
Other Locations
Japan
Akita University Hospita
RECRUITING
Akita
Chiba Cancer Center
RECRUITING
Chiba
National Hospital Organization Kyushu Cancer Center
RECRUITING
Fukuoka
Fukushima Medical University Hospital
RECRUITING
Fukushima
National Hospital Organization Fukuyama Medical Center
RECRUITING
Fukuyama
Hamamatsu University School of Medicine
NOT_YET_RECRUITING
Hamamatsu
Kansai Medical University Hospital
RECRUITING
Hirakata
Hiroshima City North Medical Center Asa Citizens Hospital
RECRUITING
Hiroshima
Hiroshima University Hospital
RECRUITING
Hiroshima
Ibaraki Prefectural Central Hospital
RECRUITING
Ibaraki
Tokai University Hospital
RECRUITING
Isehara
Social medical corporation Hakuaikai Sagara Hospital
RECRUITING
Kagoshima
National Cancer Center Hospital East
RECRUITING
Kashiwa
Saitama Medical Center
RECRUITING
Kawagoe
Kitakyushu Municipal Medical Center
RECRUITING
Kitakyushu
National Hospital Organization Kure Medical Center
RECRUITING
Kure
Gunma University Hospital
RECRUITING
Maebashi
National Hospital Organization Shikoku Cancer Center
RECRUITING
Matsuyama
Aichi Cancer Center
RECRUITING
Nagoya
Nagoya City University
RECRUITING
Nagoya
Nagoya University Hospital
RECRUITING
Nagoya
NHO Nagoya Medical Center
RECRUITING
Nagoya
Niigata Cancer Center Hospital
RECRUITING
Niigata
National Hospital Organization Nagasaki Medical Center
RECRUITING
Ōmura
National Hospital Organization Osaka National Hospital
RECRUITING
Osaka
Osaka International Cancer Institute
NOT_YET_RECRUITING
Osaka
Gunma Prefectural Cancer Center
RECRUITING
Ōta-ku
Kitasato University Hospital
RECRUITING
Sagamihara
Saitama Cancer Center
RECRUITING
Saitama
Kindai University Hospital
RECRUITING
Sakai
Hokkaido Cancer Center
RECRUITING
Sapporo
Tohoku University Hospital
RECRUITING
Sendai
Shizuoka Cancer Center
RECRUITING
Shizuoka
Shizuoka General Hospital
RECRUITING
Shizuoka
Institute of Science Tokyo Hospital
RECRUITING
Tokyo
National Cancer Center Hospital
RECRUITING
Tokyo
National Center for Global Health and Medicine
RECRUITING
Tokyo
National Hospital Organization Tokyo Medical Center
RECRUITING
Tokyo
Showa Medical University Hospital
RECRUITING
Tokyo
St.Luke's International Hospital
RECRUITING
Tokyo
The Cancer Institute Hospital of Japanese Foundation for Cancer Research
RECRUITING
Tokyo
Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital
RECRUITING
Tokyo
Tokyo Women's Medical University Hospital
NOT_YET_RECRUITING
Tokyo
Toranomon Hospital
RECRUITING
Tokyo
Mie University Hospital
RECRUITING
Tsu
Tsukuba University Hospital
RECRUITING
Tsukuba
Yamaguchi University Hospital
RECRUITING
Ube
Yao Municipal Hospital
RECRUITING
Yao
Kanagawa Cancer Center
RECRUITING
Yokohama
Contact Information
Primary
Makiko Ono, MD
makikono@gmail.com
+81333538111
Time Frame
Start Date: 2026-01-28
Estimated Completion Date: 2039-01-27
Participants
Target number of participants: 950
Treatments
Active_comparator: Upfront surgery (Arm A)
Participants in Arm A will undergo breast surgery and adjuvant systemic treatment.
Experimental: Neoadjuvant endocrine therapy (Arm B)
Participants in Arm B will receive neoadjuvant endocrine therapy of aromatase inhibitor and OFS for three months, followed by breast surgery.
Related Therapeutic Areas
Sponsors
Leads: Tokyo Women's Medical University
Collaborators: Japan Clinical Oncology Group

This content was sourced from clinicaltrials.gov