Actively Recruiting
Adjuvant Metronomic Capecitabine Plus Endocrine Therapy for HR+/HER2- Primary Breast Cancer
Led by Henan Cancer Hospital · Updated on 2024-11-04
1979
Participants Needed
1
Research Sites
361 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Breast cancer (BC) is one of most prevalent malignant tumors in the world. According to the 2020 edition of the global cancer statistics report, the incidence rate of BC has overtaken lung cancer to become the most commonly diagnosed cancer. In the past three decades, survival of patients with primary BC have been notably improved, mainly due to early detection of the disease and advances in adjuvant treatments such as endocrine therapy, chemotherapy, and anti-HER2 therapy. Patients with HR-positive and HER2-negative primary BC account for approximately 70% of all cases of early breast cancer. Endocrine therapy is the core treatment for this subtype of BC. Tamoxifen, aromatase inhibitor or their sequential administration can reduce the recurrence and mortality of this BC subtype. The results of TEXT/SOFT study showed that, compared with the traditional 5-year tamoxifen treatment, tamoxifen + OFS or aromatase inhibitor + OFS can further improve the survival of HR+/HER2- breast cancer patients. However, for premenopausal BC patients with HR+/HER2-, only 82.5% (tamoxifen plus OFS) and 85.7% (aromatase inhibitor plus OFS) of 5-year DFS were achieved. For postmenopausal BC patients, the 5-year DFS was only about 84% with aromatase inhibitors. Therefore, the survival of HR+/ HER2- BC patients needs to be further improved. Metronomic chemotherapy refers to the use of the minimum effective dose of chemotherapy drugs for long-term, uninterrupted administration to achieve anti-tumor effect. Metronomic chemotherapy has gradually been verified in clinical practice in the past 20 years. In 2020, SYSUCC-001 study has confirmed that capecitabine (650 mg/ m2 bid, for 1 years) can reduce the risk of 5-year DFS events by 36% in TNBC patients in addition to standard treatment. Besides, POTENT study has confirmed that the combination of endocrine therapy and S-1 (for one year) can further reduce the risk of iDFS by 37% in HR+/HER2- BC patients who have completed the standard treatment. Compared with capecitabine, S-1 has no indication for BC and it is not in the recommendation for BC treatment in the guidelines. Therefore, the investigators conduct this study to explore whether adjuvant Capecitabine metronomic chemotherapy for one year can further improve the survival of BC patients with HR+/ HER2- in addition to standard treatment.
CONDITIONS
Official Title
Adjuvant Metronomic Capecitabine Plus Endocrine Therapy for HR+/HER2- Primary Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 18 to 70 years
- Known menstrual status at start of treatment
- Invasive breast cancer confirmed as HR-positive and HER2-negative by histopathology
- Completed radical surgery and chemotherapy; if neoadjuvant chemotherapy was given, must have residual disease or lymph node metastasis before treatment
- Treatment within specific timelines: no more than 1 year after surgery, at least 21 days after last chemotherapy, at least 14 days after last radiotherapy, and endocrine therapy less than 6 months before study entry
- Adequate bone marrow and organ function as shown by lab tests
- Cardiac ejection fraction of 55% or higher if anthracycline chemotherapy was used
- Negative pregnancy test within 14 days before randomization for women of childbearing age
- ECOG performance status of 0 or 1
- Signed informed consent voluntarily
You will not qualify if you...
- Active double primary cancers with less than or equal to 5 years disease-free interval
- Bilateral breast cancer except if contralateral ductal carcinoma in situ has been removed by surgery
- Previous oral 5-FU treatment for more than 2 weeks
- Severe diarrhea
- Serious complications such as uncontrolled diabetes, uncontrolled hypertension, unstable angina or arrhythmias requiring treatment, cirrhosis or liver failure, interstitial pneumonia, pulmonary fibrosis, severe emphysema, active infection, or other serious conditions
- Recent myocardial infarction within 6 months
- History of fluorouracil allergy
- Pregnant or breastfeeding women
- Other conditions making patient unsuitable for the study
AI-Screening
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Trial Site Locations
Total: 1 location
1
Henan cancer hospital
Zhengzhou, Henan, China
Actively Recruiting
Research Team
Z
Zhenzhen Liu
CONTACT
J
Jiujun Zhu
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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