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Sentinel Node Biopsy in Breast Cancer: Omission of Axillary Clearance After Macrometastases. A Randomized Trial.

Primary Purpose

Breast Cancer

Status
Active
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Omission of axillary clearance
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring sentinel node biopsy, lymph node metastasis, survival

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 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

Exclusion Criteria:

  • 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.

Sites / Locations

  • Sygehus Sonderjylland
  • Aalborg University Hospital
  • Aarhus University Hospital
  • Rigshospitalet
  • Sydvestjysk Sygehus
  • Sygehus Lillebaelt
  • Odense University Hospital
  • Randers Regionshospitalet
  • Regionshospitalet Viborg
  • Athens University Hospital
  • Gävle sjukhus
  • Sahlgrenska University Hospital
  • Hallands sjukhus
  • Helsingborg lasarett
  • Länssjukhuset Ryhov
  • Kalmar sjukhus
  • Blekinge sjukhuset
  • Karlstad sjukhus
  • Central Hospital Kristianstad
  • Linköping University Hospital
  • Malmö/Lund University Hospital
  • Skaraborgs sjukhus
  • Karolinska University Hospital
  • Southern Gerenal Hospital
  • St. Görans Hospital
  • Sundsvall länssjukhus
  • Uddevalla sjukhus
  • Umeå University Hospital
  • Akademiska Sjukhuset
  • Varbergs sjukhus
  • Västervik Hospital
  • Västerås Central Hospital
  • Örebro University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Axillary clearance

No axillary clearance

Arm Description

Patients in this arm will be treated by completion axillary clearance after a sentinel node biopsy showing 1-2 nodes with macrometastasis

Patients in this arm will not undergo further axillary surgery after a sentinel node biopsy showing 1-2 nodes with macrometastasis

Outcomes

Primary Outcome Measures

breast cancer-specific survival
death due to breast cancer in both arms measured at a median follow-up of 5, 10 and 15 years

Secondary Outcome Measures

disease-free survival
Breast cancer recurrence rate in both arms after a median follow-up of 5, 10 and 15 years
axillary recurrence rate
The rate of axillary relapse in specific after a median follow-up of 5, 10 and 15 years
overall survival
The rate of overall deaths after a median follow-up of 5, 10 and 15 years

Full Information

First Posted
September 11, 2014
Last Updated
October 4, 2023
Sponsor
Karolinska Institutet
Collaborators
The Swedish Research Council, Swedish Cancer Foundation, Nordic Cancer Union
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1. Study Identification

Unique Protocol Identification Number
NCT02240472
Brief Title
Sentinel Node Biopsy in Breast Cancer: Omission of Axillary Clearance After Macrometastases. A Randomized Trial.
Official Title
Survival and Axillary Recurrence Following Sentinel Node-positive Breast Cancer Without Completion Axillary Lymph Node Dissection - a Randomized Study of Patients With Macrometastases in the Sentinel Node
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 27, 2015 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
December 31, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
The Swedish Research Council, Swedish Cancer Foundation, Nordic Cancer Union

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer
Keywords
sentinel node biopsy, lymph node metastasis, survival

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2700 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Axillary clearance
Arm Type
No Intervention
Arm Description
Patients in this arm will be treated by completion axillary clearance after a sentinel node biopsy showing 1-2 nodes with macrometastasis
Arm Title
No axillary clearance
Arm Type
Experimental
Arm Description
Patients in this arm will not undergo further axillary surgery after a sentinel node biopsy showing 1-2 nodes with macrometastasis
Intervention Type
Procedure
Intervention Name(s)
Omission of axillary clearance
Intervention Description
The intervention is the omission of completion axillary clearance after the detection of sentinel node macrometastasis
Primary Outcome Measure Information:
Title
breast cancer-specific survival
Description
death due to breast cancer in both arms measured at a median follow-up of 5, 10 and 15 years
Time Frame
up to 15 years
Secondary Outcome Measure Information:
Title
disease-free survival
Description
Breast cancer recurrence rate in both arms after a median follow-up of 5, 10 and 15 years
Time Frame
5, 10 and 15 years
Title
axillary recurrence rate
Description
The rate of axillary relapse in specific after a median follow-up of 5, 10 and 15 years
Time Frame
5, 10 and 15 years
Title
overall survival
Description
The rate of overall deaths after a median follow-up of 5, 10 and 15 years
Time Frame
5, 10 and 15 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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 Exclusion Criteria: 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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jana de Boniface, PhD
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jan Frisell, Professor
Organizational Affiliation
Karolinska University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Leif Bergkvist, Professor
Organizational Affiliation
Central Hospital Västerås
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Yvette Andersson, PhD
Organizational Affiliation
Central Hospital Västerås
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lisa Ryden, Professor
Organizational Affiliation
Lund University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Malin Sund, Professor
Organizational Affiliation
Umeå University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Olofsson Roger, PhD
Organizational Affiliation
Sahlgrenska University Hospital, Sweden
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Johan Ahlgren, PhD
Organizational Affiliation
Region Örebro County
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Dan Lundstedt, PhD
Organizational Affiliation
Sahlgrenska University Hospital, Sweden
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Peer Christiansen, Professor
Organizational Affiliation
Aarhus University Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tove Tvedskov Filtenborg, MD
Organizational Affiliation
Rigshospitalet Copenhagen, Dnmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Michalis Kontos, PhD
Organizational Affiliation
University of Athens
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Birgitte Offersen, Professor
Organizational Affiliation
University of Aarhus
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Thorsten Kühn, Professor
Organizational Affiliation
Klinikum Esslingen
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Toralf Reimer, Professor
Organizational Affiliation
Universität Rostock
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Oreste Gentilini
Organizational Affiliation
San Raffaele Hospital, Milano
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Roland Reitsamer
Organizational Affiliation
Universitätsklinikum Salzburg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sygehus Sonderjylland
City
Aabenraa
Country
Denmark
Facility Name
Aalborg University Hospital
City
Aalborg
Country
Denmark
Facility Name
Aarhus University Hospital
City
Aarhus
Country
Denmark
Facility Name
Rigshospitalet
City
Copenhagen
Country
Denmark
Facility Name
Sydvestjysk Sygehus
City
Esbjerg
Country
Denmark
Facility Name
Sygehus Lillebaelt
City
Lillebaelt
Country
Denmark
Facility Name
Odense University Hospital
City
Odense
Country
Denmark
Facility Name
Randers Regionshospitalet
City
Randers
Country
Denmark
Facility Name
Regionshospitalet Viborg
City
Viborg
Country
Denmark
Facility Name
Athens University Hospital
City
Athens
Country
Greece
Facility Name
Gävle sjukhus
City
Gävle
Country
Sweden
Facility Name
Sahlgrenska University Hospital
City
Göteborg
Country
Sweden
Facility Name
Hallands sjukhus
City
Halmstad
Country
Sweden
Facility Name
Helsingborg lasarett
City
Helsingborg
Country
Sweden
Facility Name
Länssjukhuset Ryhov
City
Jönköping
Country
Sweden
Facility Name
Kalmar sjukhus
City
Kalmar
Country
Sweden
Facility Name
Blekinge sjukhuset
City
Karlskrona
Country
Sweden
Facility Name
Karlstad sjukhus
City
Karlstad
Country
Sweden
Facility Name
Central Hospital Kristianstad
City
Kristianstad
Country
Sweden
Facility Name
Linköping University Hospital
City
Linköping
Country
Sweden
Facility Name
Malmö/Lund University Hospital
City
Lund
Country
Sweden
Facility Name
Skaraborgs sjukhus
City
Skövde/Lidköping
Country
Sweden
Facility Name
Karolinska University Hospital
City
Stockholm
Country
Sweden
Facility Name
Southern Gerenal Hospital
City
Stockholm
Country
Sweden
Facility Name
St. Görans Hospital
City
Stockholm
Country
Sweden
Facility Name
Sundsvall länssjukhus
City
Sundsvall
Country
Sweden
Facility Name
Uddevalla sjukhus
City
Uddevalla
Country
Sweden
Facility Name
Umeå University Hospital
City
Umeå
Country
Sweden
Facility Name
Akademiska Sjukhuset
City
Uppsala
Country
Sweden
Facility Name
Varbergs sjukhus
City
Varberg
Country
Sweden
Facility Name
Västervik Hospital
City
Västervik
Country
Sweden
Facility Name
Västerås Central Hospital
City
Västerås
Country
Sweden
Facility Name
Örebro University Hospital
City
Örebro
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
35279508
Citation
Appelgren M, Sackey H, Wengstrom Y, Johansson K, Ahlgren J, Andersson Y, Bergkvist L, Frisell J, Lundstedt D, Ryden L, Sund M, Alkner S, Vrou Offersen B, Filtenborg Tvedskov T, Christiansen P, de Boniface J; SENOMAC Trialists' Group. Patient-reported outcomes one year after positive sentinel lymph node biopsy with or without axillary lymph node dissection in the randomized SENOMAC trial. Breast. 2022 Jun;63:16-23. doi: 10.1016/j.breast.2022.02.013. Epub 2022 Mar 1.
Results Reference
derived
PubMed Identifier
31989379
Citation
de Boniface J, Ahlgren J, Andersson Y, Bergkvist L, Frisell J, Lundstedt D, Olofsson Bagge R, Ryden L, Sund M; SENOMAC Trialists' Group. The generalisability of randomised clinical trials: an interim external validity analysis of the ongoing SENOMAC trial in sentinel lymph node-positive breast cancer. Breast Cancer Res Treat. 2020 Feb;180(1):167-176. doi: 10.1007/s10549-020-05537-1. Epub 2020 Jan 27.
Results Reference
derived
PubMed Identifier
28549453
Citation
de Boniface J, Frisell J, Andersson Y, Bergkvist L, Ahlgren J, Ryden L, Olofsson Bagge R, Sund M, Johansson H, Lundstedt D; SENOMAC Trialists' Group. Survival and axillary recurrence following sentinel node-positive breast cancer without completion axillary lymph node dissection: the randomized controlled SENOMAC trial. BMC Cancer. 2017 May 26;17(1):379. doi: 10.1186/s12885-017-3361-y.
Results Reference
derived
Links:
URL
http://senomac.se
Description
study homepage
Available IPD and Supporting Information:
Available IPD/Information Type
Study Protocol
Available IPD/Information URL
http://senomac.se/Home/study%20protocol.html
Available IPD/Information Comments
Study protocol and patient information (English)

Learn more about this trial

Sentinel Node Biopsy in Breast Cancer: Omission of Axillary Clearance After Macrometastases. A Randomized Trial.

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