SUBMIT is a clinical trial that intends to answer the question whether up front breast surgery in patients with primary distant metastatic breast cancer will result in an improvement of the 2-year survival compared to the survival achieved with systemic therapy and delayed local treatment or systemic therapy alone. Randomization will take place immediately after the diagnosis of primary distant metastatic breast cancer. Patients either randomize for up front surgery of the breast tumor (UFS) followed by systemic therapy or for systemic therapy (ST) potentially followed by delayed local treatment of the breast tumor. The primary endpoint of this trial is the 2-years survival. Quality of life is one of the most important secondary endpoints.
In the Netherlands approximately one out of eight women will be diagnosed with breast cancer; 5% have metastatic disease at presentation. Because metastatic breast cancer is considered to be an incurable disease, it is only treated with a palliative intent. Recent retrospective studies have demonstrated that (complete) resection of the primary tumor significantly improves the outcome of patients with primary metastatic breast cancer. However, other studies showed that the survival benefit in patients who underwent surgery is caused by selection bias. SUBMIT is a clinical trial that intends to answer the question whether up front breast surgery in patients with primary distant metastatic breast cancer will result in an improvement of the 2-year survival compared to the survival achieved with systemic therapy and delayed local treatment or systemic therapy alone. Patients to submit in this study are patients with primary distant metastatic breast cancer, with no prior treatment of the breast cancer, who are 18 years or older and fit enough to undergo surgery and systemic therapy. Exclusion criteria are: history of breast cancer, other malignancy within the last 10 years, surgical treatment or radiotherapy of this breast tumor before randomization, irresectable T4 tumor or synchronous bilateral breastcancer. Randomization will take place immediately after the diagnosis of primary distant metastatic breast cancer. Patients either randomize for up front surgery of the breast tumor (UFS) followed by systemic therapy or for systemic therapy (ST) potentially followed by delayed local treatment of the breast tumor. The primary endpoint of this trial is the 2-years survival. Quality of life is one of the most important secondary endpoints.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
10
surgery of primary tumor, lumpectomy or mastectomy
chemotherapy, immunotherapy or endocrine therapy (possibly followed by local surgery of the breast)
Jeroen Bosch Ziekenhuis
's-Hertogenbosch, Netherlands
Medisch Centrum Alkmaar
Alkmaar, Netherlands
Ziekenhuisgroep Twente
Almelo, Netherlands
Wilhelmina Ziekenhuis
Assen, Netherlands
Rode Kruis Ziekenhuis
Beverwijk, Netherlands
Tergooiziekenhuizen, loc Blaricum
Blaricum, Netherlands
Reinier de Graaf
Delft, Netherlands
Catharina Ziekenhuis
Eindhoven, Netherlands
Maxima Medisch Centrum
Eindhoven, Netherlands
Atrium Medisch Centrum
Heerlen, Netherlands
...and 16 more locations
Survival
Survival is defined in months from the time of randomization until death. Overall survival will be expressed as the median survival in months.
Time frame: participants will be followed until death (expected median survival 31 months for surgery group)
Quality of Life
The EORTC QLQ - C30 and BR23 questionnaires will be used for the measurement of the quality of life. The quality of life will be assessed at 3, 6, 12, 18 months and 2,3,4,5 years after randomisation
Time frame: 5 years after randomisation
Two year survival
The percentage of patients who survive two years after randomization will be determined.
Time frame: 2 yrs after randomisation
Number of unplanned local therapies
The number of patients who will receive local treatment at another point than scheduled
Time frame: 5-6 months after randomisation
Difference in systemic therapy given
register which patients receive what treatments
Time frame: 6 months after randomisation
Determination of pathological resection margin
The definition of a complete resection in this trial means free resection margins for the invasive component.
Time frame: Pathological report approximately 1 day after surgery
Number of treatments of the axillary lymph nodes
register which patients receive these treatments
Time frame: 6 months after randomisation
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