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Surgical and Patient Reported Outcomes of Robotic Nipple-Sparing Mastectomy (RNSM)

Primary Purpose

Breast Cancer, Surgery--Complications, Genetic Predisposition to Disease

Status
Suspended
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Robotic Nipple-Sparing Mastectomy (RNSM)
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring breast surgery, robotic surgery, nipple sparing mastectomy, genetic predisposition, breast cancer

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women of any age with invasive breast cancer (BC), ductal carcinoma in situ (DCIS), BRCA or other breast cancer genetic mutation carriers or high risk BC female patients who are otherwise candidates for NSM with IPBR will be eligible for the study. For those patients, RNSM-IPBR will be offered. Those who, after thorough discussion of risks and benefits, choose and consent to undergo RNSM-IPBR will be included in the study.

Exclusion Criteria:

  • Heavy smokers (>20 cigarettes a day)
  • Uncompensated Diabetes Mellitus
  • High risk for anesthesia (ASA 4)
  • Inflammatory Breast Cancer
  • Previous thoracic radiation therapy for any reason
  • Pregnancy
  • Psychiatric, addictive, or any disorder which compromises ability to give informed consent for participation in this study

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Robotic Nipple Sparing Mastectomy Arm

Arm Description

Patient cohort undergoing nipple sparing mastectomy with use of robotic dissection.

Outcomes

Primary Outcome Measures

Feasibility of RNSM
Surgical time in minutes
Wound complications
Skin and Nipple necrosis
Margins after RNSM
Margin status (mm)
Breast cancer recurrence
Site of first relapse

Secondary Outcome Measures

Patient Satisfaction
Breast Q Pre and Post-operative Surveys- items measuring satisfaction with appearance, surgical experience, breast shape and symmetry, psychosocial, physical and sexual well being. Lowest score = 0, highest = 100 with higher scores indicating better outcomes / quality of life.
Body Image
Hopwood's Body Image Scale- Scores range from 0 (min distress) to 3 (max distress) for 10 questions. Lowest score = 0, highest = 30 with lower scores indicated lower body image distress.

Full Information

First Posted
October 30, 2019
Last Updated
April 20, 2021
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT04151368
Brief Title
Surgical and Patient Reported Outcomes of Robotic Nipple-Sparing Mastectomy
Acronym
RNSM
Official Title
Robotic Nipple-Sparing Mastectomy With Immediate Prosthetic Breast Reconstruction: Prospective Study of Feasibility, Safety and Patient Satisfaction, Toronto Experience.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Suspended
Why Stopped
Recruitment is temporarily suspended due to COVID. Will resume when appropriate.
Study Start Date
November 1, 2019 (Actual)
Primary Completion Date
November 1, 2022 (Anticipated)
Study Completion Date
November 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Nipple-sparing mastectomy (NSM) with immediate reconstruction is one of the standard of care surgical treatments of breast cancer (BC) and is used for risk reduction in patients with a high risk for BC. While this method shows satisfactory oncologic and good cosmetic outcomes, its drawbacks include compromise of the skin flap vascularization due to skin incision, nipple-areolar complex (NAC) malposition/distortion and visible scar on the breast. NSM also has technical challenges of dissecting and removing larger specimens through limited incisions and concerns regarding oncologic effectiveness due to difficulties in visualizing regions of the breast remote from the incision. To improve cosmetic outcomes after NSM, a modification of this technique using a surgical robotic system was recently described. In a limited number of studies, the robotic NSM (RNSM) with immediate prosthetic breast reconstruction (IPBR) was shown to be feasible and safe, as well as led to excellent cosmetic outcomes and patient satisfaction. There are limited number of centers in North America and none in Canada that offer RNSM-IPBR. The investigators hypothesize that RNSM-IPBR is a feasible and safe technique that can be utilized in our institution and that it can provide superior cosmetic outcomes with less morbidity and higher patient satisfaction compared to the traditional NSM-IPBR. The aim is to conduct a single-arm prospective study to investigate the safety and feasibility, as well as cosmetic, surgical complication and patient satisfaction parameters of NSM-IPBR performed in the University Health Network (UHN). This study will serve a foundation for potential introduction of a novel surgical approach in our institution and will make it available for treatment and prevention of breast cancer in Canadian women. The study will also serve as pilot data for future potential studies, including randomized-controlled trials (RCT) comparing RNSM with conventional NSM. As such, the study will further our approach to innovation in breast surgical oncology within Canada and North America.
Detailed Description
This is a single-arm prospective study to assess feasibility and safety (primary outcomes), as well as patient satisfaction, cosmetic and oncologic outcomes of RNSM-IPBR in women with BC or at high risk of BC treated at UHN. The objectives of the study are to determine: Feasibility of RNSM-IPBR through assessing operative parameters (such as time of procedure, robot docking time, conversion to conventional NSM-IPBR). Safety of RNSM-IPBR through assessing rate of morbidity from surgical complications (such as wound infection, flap and NAC necrosis, postoperative hematoma/bleeding, seroma requiring aspiration, implant loss, anesthesia related complications and need for reoperation with one month due to complications) and mortality due to the procedure. Patient satisfaction from RNSM-IPBR through assessing psychological, physical, sexual well-being, as well as satisfaction with breast, overall outcome and care through patient reported outcomes. Cosmetic outcomes of RNSM-IPBR, such as distortion or malposition of NAC and scarring, rate of reoperation due to unacceptable cosmetic outcomes. Short- and long-term oncologic outcomes of NSM-IPBR, such as positivity of margins, breast cancer incidence and recurrence rate, as well as overall survival. The rationale of the study is to investigate a novel technique of RNSM-IPBR that might have superior cosmetic and patient satisfaction outcomes, as well as lower rates of complications, based on a small number of previously published studies from Europe and Asia. Once enrolled, clinical, radiologic, and pathologic data will be collected for each participant at the initial visit and follow up data will be collected via available electronic patient records. RNSM-IPBR will be performed by previously described method (Toesca et al.) using an extra-mammary axillary incision along the mid-axillary line in the axillary fossa. We will use Da Vinci Si Surgical System® (Intuitive Surgical, Sunnyvale, CA) available at Toronto General Hospital, UHN.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Surgery--Complications, Genetic Predisposition to Disease, Surgery, BRCA1 Mutation, BRCA2 Mutation, Breast Diseases
Keywords
breast surgery, robotic surgery, nipple sparing mastectomy, genetic predisposition, breast cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective Single Arm
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robotic Nipple Sparing Mastectomy Arm
Arm Type
Experimental
Arm Description
Patient cohort undergoing nipple sparing mastectomy with use of robotic dissection.
Intervention Type
Procedure
Intervention Name(s)
Robotic Nipple-Sparing Mastectomy (RNSM)
Intervention Description
RNSM will be performed by previously described method using 3 cm extra-mammary axillary incision along the mid-axillary line in the axillary fossa. We will use Da Vinci Si Surgical System® (Intuitive Surgical, Sunnyvale, CA).
Primary Outcome Measure Information:
Title
Feasibility of RNSM
Description
Surgical time in minutes
Time Frame
1 month
Title
Wound complications
Description
Skin and Nipple necrosis
Time Frame
2 months
Title
Margins after RNSM
Description
Margin status (mm)
Time Frame
1 month
Title
Breast cancer recurrence
Description
Site of first relapse
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Patient Satisfaction
Description
Breast Q Pre and Post-operative Surveys- items measuring satisfaction with appearance, surgical experience, breast shape and symmetry, psychosocial, physical and sexual well being. Lowest score = 0, highest = 100 with higher scores indicating better outcomes / quality of life.
Time Frame
Pre-Operative and 6 and 12 months post-operative
Title
Body Image
Description
Hopwood's Body Image Scale- Scores range from 0 (min distress) to 3 (max distress) for 10 questions. Lowest score = 0, highest = 30 with lower scores indicated lower body image distress.
Time Frame
6 months post-operative

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Female patients with increased lifetime risk of breast cancer Female patients with early stage breast cancer
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women of any age with invasive breast cancer (BC), ductal carcinoma in situ (DCIS), BRCA or other breast cancer genetic mutation carriers or high risk BC female patients who are otherwise candidates for NSM with IPBR will be eligible for the study. For those patients, RNSM-IPBR will be offered. Those who, after thorough discussion of risks and benefits, choose and consent to undergo RNSM-IPBR will be included in the study. Exclusion Criteria: Heavy smokers (>20 cigarettes a day) Uncompensated Diabetes Mellitus High risk for anesthesia (ASA 4) Inflammatory Breast Cancer Previous thoracic radiation therapy for any reason Pregnancy Psychiatric, addictive, or any disorder which compromises ability to give informed consent for participation in this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tulin D Cil, MD, MEd
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G2C4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27810700
Citation
Toesca A, Peradze N, Manconi A, Galimberti V, Intra M, Colleoni M, Bonanni B, Curigliano G, Rietjens M, Viale G, Sacchini V, Veronesi P. Robotic nipple-sparing mastectomy for the treatment of breast cancer: Feasibility and safety study. Breast. 2017 Feb;31:51-56. doi: 10.1016/j.breast.2016.10.009. Epub 2016 Nov 2.
Results Reference
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PubMed Identifier
29959612
Citation
Sarfati B, Struk S, Leymarie N, Honart JF, Alkhashnam H, Tran de Fremicourt K, Conversano A, Rimareix F, Simon M, Michiels S, Kolb F. Robotic Prophylactic Nipple-Sparing Mastectomy with Immediate Prosthetic Breast Reconstruction: A Prospective Study. Ann Surg Oncol. 2018 Sep;25(9):2579-2586. doi: 10.1245/s10434-018-6555-x. Epub 2018 Jun 29.
Results Reference
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Surgical and Patient Reported Outcomes of Robotic Nipple-Sparing Mastectomy

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