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Systemic Therapy With or Without Upfront Surgery in Metastatic Breast Cancer (SUBMIT)

Primary Purpose

Metastatic Breast Cancer

Status
Terminated
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
upfront breast surgery
systemic therapy
Sponsored by
Jeroen Bosch Ziekenhuis
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Metastatic Breast Cancer focused on measuring survival, systemic therapy, upfront surgery

Eligibility Criteria

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

Inclusion Criteria:

  • Newly diagnosed primary distant metastatic breast cancer (M1)
  • Anticipated survival of at least 6 months
  • Histologically proven breast cancer
  • Hormonal and HER2Neu status should be known
  • T1-T3, resectable T4 status, N0-N3
  • Performance status of the patient should allow surgery / systemic therapy
  • Co-morbidity of the patient should allow surgery / systemic therapy
  • Age > 18 years
  • Written informed consent

Exclusion Criteria:

  • Primary invasive breast cancer in medical history
  • Other malignancy within the last 10 years, besides basal cell carcinoma of the skin or early stage cervical cancer
  • Surgical treatment / radiotherapy of this breast tumor before randomization
  • Irresectable T4 breast tumor
  • Synchronous bilateral breast cancer

Sites / Locations

  • Medisch Centrum Alkmaar
  • Ziekenhuisgroep Twente
  • Wilhelmina Ziekenhuis
  • Rode Kruis Ziekenhuis
  • Tergooiziekenhuizen, loc Blaricum
  • Reinier de Graaf
  • Jeroen Bosch Ziekenhuis
  • Haga Ziekenhuis, Loc. Leijweg
  • Ziekenhuis Bronovo
  • Catharina Ziekenhuis
  • Maxima Medisch Centrum
  • Atrium Medisch Centrum
  • Ziekenhuis Elkerliek, loc Helmond
  • Ziekenhuisgroep Twente, Loc. SMT
  • Spaarne Ziekenhuis
  • Medisch Centrum Leeuwarden
  • Diaconessenhuis
  • Maastricht University Medical Center
  • St. Antonius Ziekenhuis, Loc. Nieuwegein
  • Canisius-Wilhelmina Ziekenhuis
  • UMC St. Radboud
  • Ikazia Ziekenhuis
  • Orbis Medisch Centrum
  • St. Elisabeth Ziekenhuis
  • Viecuri Medisch Centrum, loc. St Maartens Gasthuis
  • Isala Klinieken

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Upfront surgery

Systemic therapy

Arm Description

Upfront surgery followed by systemic treatment

Systemic therapy possibly followed by local treatment of the breast tumor

Outcomes

Primary Outcome Measures

Survival
Survival is defined in months from the time of randomization until death. Overall survival will be expressed as the median survival in months.

Secondary Outcome Measures

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
Two year survival
The percentage of patients who survive two years after randomization will be determined.
Number of unplanned local therapies
The number of patients who will receive local treatment at another point than scheduled
Difference in systemic therapy given
register which patients receive what treatments
Determination of pathological resection margin
The definition of a complete resection in this trial means free resection margins for the invasive component.
Number of treatments of the axillary lymph nodes
register which patients receive these treatments

Full Information

First Posted
July 5, 2011
Last Updated
February 2, 2014
Sponsor
Jeroen Bosch Ziekenhuis
Collaborators
Borstkanker Onderzoek Groep, Comprehensive Cancer Centre The Netherlands
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1. Study Identification

Unique Protocol Identification Number
NCT01392586
Brief Title
Systemic Therapy With or Without Upfront Surgery in Metastatic Breast Cancer
Acronym
SUBMIT
Official Title
Systemic Therapy With or Without Up Front Surgery of the Primary Tumor in Breast Cancer Patients With Distant Metastases at Initial presenTation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Terminated
Why Stopped
due to low accrual rate
Study Start Date
February 2012 (undefined)
Primary Completion Date
January 2014 (Actual)
Study Completion Date
January 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Jeroen Bosch Ziekenhuis
Collaborators
Borstkanker Onderzoek Groep, Comprehensive Cancer Centre The Netherlands

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Metastatic Breast Cancer
Keywords
survival, systemic therapy, upfront surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Upfront surgery
Arm Type
Experimental
Arm Description
Upfront surgery followed by systemic treatment
Arm Title
Systemic therapy
Arm Type
Other
Arm Description
Systemic therapy possibly followed by local treatment of the breast tumor
Intervention Type
Procedure
Intervention Name(s)
upfront breast surgery
Intervention Description
surgery of primary tumor, lumpectomy or mastectomy
Intervention Type
Other
Intervention Name(s)
systemic therapy
Intervention Description
chemotherapy, immunotherapy or endocrine therapy (possibly followed by local surgery of the breast)
Primary Outcome Measure Information:
Title
Survival
Description
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)
Secondary Outcome Measure Information:
Title
Quality of Life
Description
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
Title
Two year survival
Description
The percentage of patients who survive two years after randomization will be determined.
Time Frame
2 yrs after randomisation
Title
Number of unplanned local therapies
Description
The number of patients who will receive local treatment at another point than scheduled
Time Frame
5-6 months after randomisation
Title
Difference in systemic therapy given
Description
register which patients receive what treatments
Time Frame
6 months after randomisation
Title
Determination of pathological resection margin
Description
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
Title
Number of treatments of the axillary lymph nodes
Description
register which patients receive these treatments
Time Frame
6 months after randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newly diagnosed primary distant metastatic breast cancer (M1) Anticipated survival of at least 6 months Histologically proven breast cancer Hormonal and HER2Neu status should be known T1-T3, resectable T4 status, N0-N3 Performance status of the patient should allow surgery / systemic therapy Co-morbidity of the patient should allow surgery / systemic therapy Age > 18 years Written informed consent Exclusion Criteria: Primary invasive breast cancer in medical history Other malignancy within the last 10 years, besides basal cell carcinoma of the skin or early stage cervical cancer Surgical treatment / radiotherapy of this breast tumor before randomization Irresectable T4 breast tumor Synchronous bilateral breast cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
M.F. Ernst, dr
Organizational Affiliation
Jeroen Bosch Ziekenhuis
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
A.C. Voogd, dr
Organizational Affiliation
Maastricht University Medical Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
V.C.G. Tjan-Heijnen, Prof, dr
Organizational Affiliation
Maastricht University Medical Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medisch Centrum Alkmaar
City
Alkmaar
Country
Netherlands
Facility Name
Ziekenhuisgroep Twente
City
Almelo
Country
Netherlands
Facility Name
Wilhelmina Ziekenhuis
City
Assen
Country
Netherlands
Facility Name
Rode Kruis Ziekenhuis
City
Beverwijk
Country
Netherlands
Facility Name
Tergooiziekenhuizen, loc Blaricum
City
Blaricum
Country
Netherlands
Facility Name
Reinier de Graaf
City
Delft
Country
Netherlands
Facility Name
Jeroen Bosch Ziekenhuis
City
Den Bosch
Country
Netherlands
Facility Name
Haga Ziekenhuis, Loc. Leijweg
City
Den Haag
Country
Netherlands
Facility Name
Ziekenhuis Bronovo
City
Den Haag
Country
Netherlands
Facility Name
Catharina Ziekenhuis
City
Eindhoven
Country
Netherlands
Facility Name
Maxima Medisch Centrum
City
Eindhoven
Country
Netherlands
Facility Name
Atrium Medisch Centrum
City
Heerlen
Country
Netherlands
Facility Name
Ziekenhuis Elkerliek, loc Helmond
City
Helmond
Country
Netherlands
Facility Name
Ziekenhuisgroep Twente, Loc. SMT
City
Hengelo
Country
Netherlands
Facility Name
Spaarne Ziekenhuis
City
Hoofddorp
Country
Netherlands
Facility Name
Medisch Centrum Leeuwarden
City
Leeuwarden
Country
Netherlands
Facility Name
Diaconessenhuis
City
Leiden
Country
Netherlands
Facility Name
Maastricht University Medical Center
City
Maastricht
Country
Netherlands
Facility Name
St. Antonius Ziekenhuis, Loc. Nieuwegein
City
Nieuwegein
Country
Netherlands
Facility Name
Canisius-Wilhelmina Ziekenhuis
City
Nijmegen
Country
Netherlands
Facility Name
UMC St. Radboud
City
Nijmegen
Country
Netherlands
Facility Name
Ikazia Ziekenhuis
City
Rotterdam
Country
Netherlands
Facility Name
Orbis Medisch Centrum
City
Sittard
Country
Netherlands
Facility Name
St. Elisabeth Ziekenhuis
City
Tilburg
Country
Netherlands
Facility Name
Viecuri Medisch Centrum, loc. St Maartens Gasthuis
City
Venlo
Country
Netherlands
Facility Name
Isala Klinieken
City
Zwolle
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
22469291
Citation
Ruiterkamp J, Voogd AC, Tjan-Heijnen VC, Bosscha K, van der Linden YM, Rutgers EJ, Boven E, van der Sangen MJ, Ernst MF; Dutch Breast Cancer Trialists' Group (BOOG). SUBMIT: Systemic therapy with or without up front surgery of the primary tumor in breast cancer patients with distant metastases at initial presentation. BMC Surg. 2012 Apr 2;12:5. doi: 10.1186/1471-2482-12-5.
Results Reference
derived

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Systemic Therapy With or Without Upfront Surgery in Metastatic Breast Cancer

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