Sentinel Node Biopsy in Breast Cancer: Omission of Axillary Clearance After Macrometastases. A Randomized Trial.
- Conditions
- Breast Cancer
- Interventions
- Procedure: Omission of axillary clearance
- Registration Number
- NCT02240472
- Lead Sponsor
- Karolinska Institutet
- Brief Summary
Since the introduction of sentinel node biopsy in breast cancer, it has become clear that its use is reliable and reproducible. Today, it is clinical routine to not remove further lymph nodes from the axilla (arm pit) in case the sentinel node (which is the first lymph node/s reached by lymphatic flow from the breast) is free of tumor deposits. It is also routine to leave remaining lymph nodes behind in case the sentinel node contains a minimal cluster of tumor cells, called isolated tumor cells (formerly submicrometastasis). Even in slightly larger tumor deposits, so called micrometastasis (up to 2 mm in size), it has been shown that a completion axillary clearance (removal of further lymph nodes from the arm pit) does not contribute to a better survival. Data from a randomized study indicate that it seems safe to omit axillary clearance even if the sentinel node biopsy shows up to 2 nodes with tumor deposits over 2 mm in size (macrometastasis). These studies have changed clinical practice in many countries, however, it is still debated whether it is safe to omit axillary clearance in the case of sentinel node macrometastasis due to under-recruitment in the aforementioned study. The rationale for omitting extensive axillary surgery is the avoidance of postoperative morbidity such as arm lymphedema, loss of sensation, pain and swelling.
The hypothesis is that refraining from axillary clearance in breast cancer patients with 1-2 sentinel nodes with macrometastasis will not worsen breast cancer-specific survival by more than a maximum of 2.5% after 5 years.
This study is a prospective international randomized trial including 3500 patients.
Breast cancer patients without signs of axillary nodal involvement will be eligible for sentinel node biopsy. Those who are found to have up to two sentinel node containing macrometastasis will be informed about this trial Those wishing to participate will be randomized to either undergo further axillary surgery (clearance) or not. Outcome measures are breast cancer-specific survival, disease-free survival, axillary recurrence rate and overall survival.
- Detailed Description
Details can be found on www.senomac.se
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 2700
- Patients with invasive breast cancer (T1-T3)
- N0 on palpation
- Preoperative ultrasound performed
- Pathology report shows macrometastasis in 1-2 sentinel lymph nodes
- Patients undergo breast-conserving therapy or mastectomy
- The patient must have provided oral and written consent
- Age ≥ 18 years
- Metastases outside of the ipsilateral axilla
- Prior history of invasive breast cancer
- Pregnancy
- Bilateral breast cancer if one side meets exclusion criteria
- Medical contraindication for radiotherapy or systemic treatment
- Inability to absorb or understand the meaning of the study information; for example, through disability, inadequate language skills or dementia.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description No axillary clearance Omission of axillary clearance Patients in this arm will not undergo further axillary surgery after a sentinel node biopsy showing 1-2 nodes with macrometastasis
- Primary Outcome Measures
Name Time Method breast cancer-specific survival up to 15 years death due to breast cancer in both arms measured at a median follow-up of 5, 10 and 15 years
- Secondary Outcome Measures
Name Time Method axillary recurrence rate 5, 10 and 15 years The rate of axillary relapse in specific after a median follow-up of 5, 10 and 15 years
disease-free survival 5, 10 and 15 years Breast cancer recurrence rate in both arms after a median follow-up of 5, 10 and 15 years
overall survival 5, 10 and 15 years The rate of overall deaths after a median follow-up of 5, 10 and 15 years
Trial Locations
- Locations (33)
Athens University Hospital
🇬🇷Athens, Greece
Sydvestjysk Sygehus
🇩🇰Esbjerg, Denmark
Odense University Hospital
🇩🇰Odense, Denmark
Aalborg University Hospital
🇩🇰Aalborg, Denmark
Sygehus Sonderjylland
🇩🇰Aabenraa, Denmark
Aarhus University Hospital
🇩🇰Aarhus, Denmark
Sygehus Lillebaelt
🇩🇰Lillebaelt, Denmark
Randers Regionshospitalet
🇩🇰Randers, Denmark
Regionshospitalet Viborg
🇩🇰Viborg, Denmark
Gävle sjukhus
🇸🇪Gävle, Sweden
Länssjukhuset Ryhov
🇸🇪Jönköping, Sweden
Hallands sjukhus
🇸🇪Halmstad, Sweden
Helsingborg lasarett
🇸🇪Helsingborg, Sweden
Kalmar sjukhus
🇸🇪Kalmar, Sweden
Karlstad sjukhus
🇸🇪Karlstad, Sweden
Malmö/Lund University Hospital
🇸🇪Lund, Sweden
Central Hospital Kristianstad
🇸🇪Kristianstad, Sweden
Linköping University Hospital
🇸🇪Linköping, Sweden
Skaraborgs sjukhus
🇸🇪Skövde/Lidköping, Sweden
Varbergs sjukhus
🇸🇪Varberg, Sweden
Karolinska University Hospital
🇸🇪Stockholm, Sweden
Sundsvall länssjukhus
🇸🇪Sundsvall, Sweden
Southern Gerenal Hospital
🇸🇪Stockholm, Sweden
St. Görans Hospital
🇸🇪Stockholm, Sweden
Uddevalla sjukhus
🇸🇪Uddevalla, Sweden
Akademiska Sjukhuset
🇸🇪Uppsala, Sweden
Umeå University Hospital
🇸🇪Umeå, Sweden
Örebro University Hospital
🇸🇪Örebro, Sweden
Västervik Hospital
🇸🇪Västervik, Sweden
Västerås Central Hospital
🇸🇪Västerås, Sweden
Rigshospitalet
🇩🇰Copenhagen, Denmark
Sahlgrenska University Hospital
🇸🇪Göteborg, Sweden
Blekinge sjukhuset
🇸🇪Karlskrona, Sweden