Actively Recruiting

Age: 18Years - 90Years
FEMALE
NCT06888388

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

Age: 18Years - 90Years
FEMALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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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

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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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