Bone Metastases, Breast Cancer, Stage IV Breast Cancer
Conditions
Keywords
Breast Cancer, Stage IV, Bone Metastasis
Brief summary
This is a national multicenter, prospective, randomized controlled trial. The study aims to compare the 5-year overall survival (OS) between patients receiving primary tumor surgery followed by systemic therapy (surgery group) and those receiving systemic therapy alone (non-surgery group) in patients with de novo Stage IV breast cancer who have solitary bone metastases. Secondary objectives include comparing progression-free survival (PFS), breast cancer-specific survival (BCSS), local control rates, patient-reported outcomes (BREAST-Q, QLQ-C30), safety (surgical complications and systemic therapy toxicities), and cost-effectiveness.
Detailed description
The value of primary tumor resection in de novo stage IV breast cancer (BC) remains debated. While early retrospective studies suggested a potential survival benefit, recent large-scale randomized controlled trials (e.g., JCOG1017, E2108) have shown no OS benefit for the overall stage IV BC population. However, exploratory subgroup analyses consistently point towards a potential benefit for patients with hormone receptor-positive (HR+) disease and low metastatic burden, such as solitary bone metastases. Given the unique biological behavior of HR+ BC and the effectiveness of modern systemic therapies (e.g., endocrine therapy + CDK4/6 inhibitors), it is hypothesized that primary tumor surgery may provide an additional "consolidation" benefit in this specific subgroup by improving local control and potentially prolonging survival. To address this, our team has designed this national multicenter, prospective, randomized controlled trial. This study will enroll patients with de novo stage IV BC confirmed to have only bone metastases. All participants will receive standard systemic therapy based on their molecular subtype. Participants will be randomized 1:1 to either undergo primary tumor surgery (mastectomy or breast-conserving surgery with or without immediate reconstruction) within 4 weeks of randomization, followed by continued systemic therapy, or to receive systemic therapy alone. Palliative radiotherapy for bone metastases is permitted in both arms. The primary endpoint is 5-year overall survival. Secondary endpoints include PFS, BCSS, local control rate, quality of life (BREAST-Q, QLQ-C30), surgical complication rates, and cost analysis. This study will provide high-level evidence to guide personalized treatment decisions for this specific patient subgroup in China.
Interventions
PROCEDUREPrimary Tumor Resection
Surgical removal of the primary breast tumor. The procedure type (mastectomy or breast-conserving surgery) is determined by tumor size, location, and patient preference, and is performed by experienced breast surgeons following national guidelines. Axillary staging (sentinel node biopsy or dissection) is performed concurrently. Immediate breast reconstruction (prosthesis or autologous tissue) may be performed when indicated.
Systemic treatment administered according to the patient's molecular subtype (HR+, HER2+, or Triple-negative) based on Chinese and international clinical guidelines. Regimens include, but are not limited to, endocrine therapy (e.g., letrozole, exemestane) with or without CDK4/6 inhibitors (e.g., palbociclib) for HR+/HER2- disease; anti-HER2 targeted therapy (e.g., trastuzumab, pertuzumab) combined with chemotherapy for HER2+ disease; and chemotherapy (e.g., taxanes, anthracyclines) with or without immunotherapy (e.g., pembrolizumab) for triple-negative disease. All patients with bone metastases routinely receive bone-modifying agents (zoledronic acid or denosumab).
Sponsors
West China Hospital
The Second Affiliated Hospital of Hunan University of Traditional Chinese Medicine
The First Affiliated Hospital of Zhengzhou University
The Nineth Hospital of Shenzhen, Longgang Center Hospital
Baotou Cancer Hospital
Hebei General Hospital
General Hospital of Ningxia Medical University
The First Hospital of Jilin University
Tangshan People's Hospital
Guangdong Women and Children Hospital
Nanchang People's Hospital
Cancer Hospital of Guangxi Medical University
Xinjiang Medical University Cancer Hospital
Anyang Tumor Hospital
The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine
Shanxi Bethune Hospital
Hebei Medical University Fourth Hospital
The Affiliated Hospital of Qingdao University
Suzhou Municipal Hospital
Zhejiang Provincial People's Hospital
Hunan Cancer Hospital
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Shanxi Province Cancer Hospital
The First Hospital of Lanzhou University, Gansu, China
Lanzhou University Second Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Female patients aged 18 to 70 years (inclusive); * Histopathologically confirmed (by core needle biopsy) invasive breast cancer; * Diagnosed with de novo Stage IV breast cancer with metastases confirmed to be limited to bone; * Patients may be enrolled either at initial diagnosis or after receiving first-line systemic therapy; * Willing and able to provide written informed consent.
Exclusion criteria
* Disease progression (per RECIST 1.1 criteria) in the primary tumor, regional lymph nodes, or bone metastases after first-line systemic therapy; * Presence of other primary malignancies; * Severe comorbidities that would preclude surgery or safe administration of systemic therapy (e.g., severe cardiopulmonary disease, uncontrolled diabetes, long-term smoking history with poor pulmonary function, immunodeficiency); * Current participation in another clinical trial that would interfere with the outcomes of this study; * Refusal to provide informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival (OS) | 5 years post-randomization | Time from randomization to death from any cause. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall Survival (OS) | 3 and 10 years post-randomization | Time from randomization to death from any cause. |
| Progression-Free Survival (PFS) | Up to 10 years post-randomization | Time from randomization to first documented disease progression (local progression, regional recurrence, or new/ progressive distant metastases) or death from any cause. |
| Breast Cancer-Specific Survival (BCSS) | Up to 10 years post-randomization | Time from randomization to death due to breast cancer. |
| Patient-Reported Outcomes (PROs) | Baseline, 6 months, 5 years, and 10 years post-randomization. | Quality of life measured by the EORTC QLQ-C30 (global health status/QoL). |
Contacts
CONTACTZhenggui Du
CONTACTLiuying Li
Outcome results
None listed