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Does Autologous Fat Transplantation Improve Results and Reduce Complications in Breast Reconstruction With Implants?

Primary Purpose

Breast Neoplasms

Status
Unknown status
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Autologous fat transplantation
Expander prosthesis
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Neoplasms focused on measuring Mammaplasty, Transplantation, Autologous, Mastectomy, Breast Implants, Radiotherapy, Adjuvant

Eligibility Criteria

25 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Previously undergone mastectomy and adjuvant radiotherapy.
  • Will undergo breast reconstruction with expander prosthesis.
  • Mammogram and ultrasound performed maximum three month prior surgery.
  • At least one year since last operation or radiotherapy.

Exclusion Criteria:

  • Known breast cancer relapse
  • Distant metastases except axillary
  • Any contraindication for anaesthesia
  • Systemic disease such as diabetes mellitus type I.
  • BMI >30 (if the patients lose weight they are eligible)

Sites / Locations

  • Karolinska Institutet, Department of Molecular Medicine and Surgery, Karolinska University Hospital, Department of Reconstructive Plastic Surgery

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Breast reconstruction with implant

Autologous fat transplantation

Arm Description

The patients will undergo breast reconstruction with an expander prosthesis.

The patients will undergo lipofilling as a pre-treatment before they will undergo breast reconstruction with an expander prosthesis.

Outcomes

Primary Outcome Measures

Frequency of reoperations
Frequency of complications

Secondary Outcome Measures

Total days in hospital during fat transplantation and reconstruction with prosthesis
Number of days spent at the hospital for surgery including both day surgery with fat transplantation and reconstruction with prosthesis.
Number of appointments as outpatient after breast reconstruction.
Number of appointments with surgeon and nurse as outpatient after the reconstructive surgery is performed.
Aesthetic evaluation of the results of the breast reconstruction
Aesthetic outcome is evaluated by plastic surgeons through assessment of standardized photographies of the patients.
Patient reported outcome
Breast Q is a validated questionnaire for quality of life

Full Information

First Posted
December 22, 2014
Last Updated
April 15, 2019
Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02637635
Brief Title
Does Autologous Fat Transplantation Improve Results and Reduce Complications in Breast Reconstruction With Implants?
Official Title
Does Pre-treatment With Autologous Fat Transplantation Improve Results and Reduce Complication Rate After Breast Reconstruction With Implants? A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 2012 (undefined)
Primary Completion Date
January 2020 (Anticipated)
Study Completion Date
January 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
Karolinska University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine if autologous fat transplantation as a pre-treatment gives better results in breast reconstruction with implants after mastectomy and radiotherapy. One group is randomized to conventional reconstruction with implant and one to pre-treatment prior reconstruction with implant. Our aims are: To study whether lipofilling can decrease the number of reoperations and complications such as postoperative infections or not. Evaluate the aesthetic results and the patients' experiences. For both these aims the hypothesis is that pre-treatment is in favour for the outcomes.
Detailed Description
All patients will undergo breast reconstruction with expander implant. Half of the patients will be randomized to pre-treatment with lipofilling before the reconstruction. The randomization will be carried out with block randomization. A certain person that has not met the patients has been assigned to do this. Fat transplantation: The fat will be harvested manually with dry technique using a Coleman cannula on a 10 ml syringe. There after the syringes and fat are centrifuged at 3000 rpm for 3 minutes. Liquid fat from lysed cells and blood will be separated from the purified fat cells and discarded. The fat graft will then be injected fan-shaped in multiple layers into the subcutaneous tissues of the breast using another blunt cannula with a diameter of 1.29 mm. If necessary to obtain a volume of 100 ml fat injected the procedure will be repeated. All sessions will be performed under general anesthesia in day surgery. Three month later the patients will undergo breast reconstruction with expander prosthesis. Those patients that are randomized to not undergo pre-treatment will undergo breast reconstruction with expander prosthesis immediately. After the reconstruction all patients will have as many appointments as necessary for expansion with a breast nurse at our clinic. If necessary the patient will also meet the surgeon. After the month the patients have a routine doctors appointment. After 6, 12 and 24 month the patients will be followed up with objective measurements of breast symmetry and they will fill in quality of life formularies. In this study we are using the validated formulary called Breast Q and a study specific formulary. At 24 month standardized photos of the breasts will be taken.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasms
Keywords
Mammaplasty, Transplantation, Autologous, Mastectomy, Breast Implants, Radiotherapy, Adjuvant

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Breast reconstruction with implant
Arm Type
Experimental
Arm Description
The patients will undergo breast reconstruction with an expander prosthesis.
Arm Title
Autologous fat transplantation
Arm Type
Experimental
Arm Description
The patients will undergo lipofilling as a pre-treatment before they will undergo breast reconstruction with an expander prosthesis.
Intervention Type
Procedure
Intervention Name(s)
Autologous fat transplantation
Other Intervention Name(s)
lipofilling, fat grafting, lipomodelling
Intervention Description
100 ml of autologous fat will be injected to the reconstruction area 3 month prior the breast reconstruction with expander prosthesis.
Intervention Type
Procedure
Intervention Name(s)
Expander prosthesis
Other Intervention Name(s)
implant
Intervention Description
breast reconstruction with expander prosthesis.
Primary Outcome Measure Information:
Title
Frequency of reoperations
Time Frame
Two years on from reconstruction with prosthesis
Title
Frequency of complications
Time Frame
Two years on from reconstruction with prosthesis
Secondary Outcome Measure Information:
Title
Total days in hospital during fat transplantation and reconstruction with prosthesis
Description
Number of days spent at the hospital for surgery including both day surgery with fat transplantation and reconstruction with prosthesis.
Time Frame
4 month
Title
Number of appointments as outpatient after breast reconstruction.
Description
Number of appointments with surgeon and nurse as outpatient after the reconstructive surgery is performed.
Time Frame
Two years on from reconstruction with prosthesis
Title
Aesthetic evaluation of the results of the breast reconstruction
Description
Aesthetic outcome is evaluated by plastic surgeons through assessment of standardized photographies of the patients.
Time Frame
Two years on from reconstruction with prosthesis
Title
Patient reported outcome
Description
Breast Q is a validated questionnaire for quality of life
Time Frame
Measured at 6, 12 and 24 month from reconstruction with prosthesis

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Previously undergone mastectomy and adjuvant radiotherapy. Will undergo breast reconstruction with expander prosthesis. Mammogram and ultrasound performed maximum three month prior surgery. At least one year since last operation or radiotherapy. Exclusion Criteria: Known breast cancer relapse Distant metastases except axillary Any contraindication for anaesthesia Systemic disease such as diabetes mellitus type I. BMI >30 (if the patients lose weight they are eligible)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Inkeri Schultz, PhD
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Åsa Edsander-Nord, Docent
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Marie Wickman Chantereau, Professor
Official's Role
Study Director
Facility Information:
Facility Name
Karolinska Institutet, Department of Molecular Medicine and Surgery, Karolinska University Hospital, Department of Reconstructive Plastic Surgery
City
Stockholm
ZIP/Postal Code
17177
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
20048576
Citation
Serra-Renom JM, Munoz-Olmo JL, Serra-Mestre JM. Fat grafting in postmastectomy breast reconstruction with expanders and prostheses in patients who have received radiotherapy: formation of new subcutaneous tissue. Plast Reconstr Surg. 2010 Jan;125(1):12-18. doi: 10.1097/PRS.0b013e3181c49458.
Results Reference
background
PubMed Identifier
17415234
Citation
Rigotti G, Marchi A, Galie M, Baroni G, Benati D, Krampera M, Pasini A, Sbarbati A. Clinical treatment of radiotherapy tissue damage by lipoaspirate transplant: a healing process mediated by adipose-derived adult stem cells. Plast Reconstr Surg. 2007 Apr 15;119(5):1409-1422. doi: 10.1097/01.prs.0000256047.47909.71.
Results Reference
background
PubMed Identifier
21514910
Citation
Sarfati I, Ihrai T, Kaufman G, Nos C, Clough KB. Adipose-tissue grafting to the post-mastectomy irradiated chest wall: preparing the ground for implant reconstruction. J Plast Reconstr Aesthet Surg. 2011 Sep;64(9):1161-6. doi: 10.1016/j.bjps.2011.03.031. Epub 2011 Apr 22.
Results Reference
background
PubMed Identifier
19730294
Citation
Mojallal A, Lequeux C, Shipkov C, Breton P, Foyatier JL, Braye F, Damour O. Improvement of skin quality after fat grafting: clinical observation and an animal study. Plast Reconstr Surg. 2009 Sep;124(3):765-774. doi: 10.1097/PRS.0b013e3181b17b8f.
Results Reference
background
Links:
URL
http://www.swebcg.se/index.asp?P=Start
Description
Swedish Breast Cancer Group. Provides national guidelines for breast cancer treatment etc.

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Does Autologous Fat Transplantation Improve Results and Reduce Complications in Breast Reconstruction With Implants?

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