Actively Recruiting
Long-term Safety of Nipple Sparing Mastectomy in Women With High Penetrance Breast Cancer Susceptibility Genes in Breast Cancer
Led by Sir Mortimer B. Davis - Jewish General Hospital · Updated on 2025-12-08
4700
Participants Needed
12
Research Sites
156 weeks
Total Duration
On this page
Sponsors
S
Sir Mortimer B. Davis - Jewish General Hospital
Lead Sponsor
C
Cancer Research Society
Collaborating Sponsor
AI-Summary
What this Trial Is About
Patients with a germline pathogenic variant (GPV) in high-penetrance breast cancer susceptibility genes who are considering risk reducing mastectomy (RRM) often strongly desire to keep their nipple areola complex but inquire as to whether it is safe to do so. Relative to traditional or skin sparing mastectomy (SSM) techniques, nipple sparing mastectomy (NSM) is associated with improved psychosocial and sexual well-being and is significantly better for body image and reducing feelings of disfigurement. Despite this, guidelines have yet to endorse the use of NSM over other RRM techniques, stating that more data and longer follow-up are needed to confirm it as a safe and effective strategy in GPV carriers. As NSM was not routinely adopted in high-risk patient populations undergoing RRM before 2010, there has been little data to inform the long-term oncologic safety of NSM. Well-designed studies have reported low to negligible rates of subsequent breast cancer in BRCA1/2 carriers following NSM, but have been limited by short median follow-up of less than 3 years. The current study is designed to confirm, with longer follow-up, prior findings on the oncologic safety of NSM in unaffected BRCA1/2 carriers. The investigators will also expand data to other high-penetrance GPV carriers, including PALB2, CDH1, PTEN, and TP53, for whom there is little-to-no data on outcomes following RRM.
CONDITIONS
Official Title
Long-term Safety of Nipple Sparing Mastectomy in Women With High Penetrance Breast Cancer Susceptibility Genes in Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Assigned female sex at birth
- Age 18 years or older
- Confirmed germline pathogenic variant (GPV) in BRCA1, BRCA2, PALB2, TP53, CDH1, or PTEN found through presymptomatic genetic testing
You will not qualify if you...
- History of breast cancer before genetic testing
- History of ovarian cancer before genetic testing
- History of bilateral mastectomy before genetic testing
- Presence of a variant of uncertain significance (VUS) without another confirmed GPV in BRCA1, BRCA2, PALB2, TP53, CDH1, or PTEN
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 12 locations
1
Yale University
New Haven, Connecticut, United States, 06510
Actively Recruiting
2
Brigham and Women's Hospital - Dana-Farber Brigham Cancer Center
Boston, Massachusetts, United States, 02115
Not Yet Recruiting
3
Memorial Sloan Kettering Cancer Center (MSKCC)
New York, New York, United States, 10065
Not Yet Recruiting
4
University of Pennsylvania
Philadelphia, Pennsylvania, United States, 19104-6205
Actively Recruiting
5
University of Melbourne, Peter MacCallum Cancer Center
Melbourne, Australia
Not Yet Recruiting
6
Ziekenhuis Aan de Stroom
Antwerp, Belgium, 2030
Active, Not Recruiting
7
University of Calgary
Calgary, Alberta, Canada, T2N 4N1
Actively Recruiting
8
Hamilton Health Sciences
Hamilton, Ontario, Canada, L8L 2X2
Actively Recruiting
9
Women's College Hospital, University of Toronto
Toronto, Ontario, Canada
Not Yet Recruiting
10
Jewish General Hospital
Montreal, Quebec, Canada, H3T1E2
Actively Recruiting
11
CHU de Quebec Université laval
Québec, Quebec, Canada, G1S 4L8
Actively Recruiting
12
Champalimaud Foundation, University of Lisbon
Lisbon, Portugal
Not Yet Recruiting
Research Team
S
Stephanie Wong, MD
CONTACT
S
Sarah Sabboobeh, MSc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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