Long-term Safety of Nipple Sparing Mastectomy in Women With High Penetrance Breast Cancer Susceptibility Genes in Breast Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-90
SponsorSir Mortimer B. Davis - Jewish General Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Assigned female sex at birth

Age 18 years or older

Confirmed GPV in BRCA1, BRCA2, PALB2, TP53, CDH1 or PTEN identified on pre-symptomatic genetic testing

Disqualifiers

History of breast cancer prior to genetic testing

History of ovarian cancer prior to genetic testing

History of bilateral mastectomy performed prior to genetic testing

Presence of a variant of uncertain significance (VUS) in the absence of another GPV in BRCA1, BRCA2, PALB2, TP53, CDH1 or PTEN.

Trial population

Female patients aged 18-years or older with a confirmed GPV in BRCA1, BRCA2, PALB2, TP53, CDH1 or PTEN identified on pre-symptomatic genetic testing performed between January 1, 1994-June 30, 2024

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Nipple Sparing Mastectomy (NSM)

    Procedure/Surgery

    Nipple sparing mastectomy (NSM) is a surgical procedure which removes all macroscopic breast glandular tissue while retaining the skin as well as the nipple areola complex.

  • Skin-Sparing Mastectomy (SSM)

    Procedure/Surgery

    Skin sparing mastectomy (SSM) is a procedure that removes the nipple and areola complex along with all visible macroscopic breast glandular tissue.

  • Total (Simple) Mastectomy

    Procedure/Surgery

    Total (Simple) Mastectomy is a traditional mastectomy approach that removes the breast glandular tissue with a large overlying area of skin including the nipple and areola complex to allow for flat closure.

Treatment groups

4,700 Participants
are divided into 2 treatment groups
Group A: Risk Reducing Mastectomy3 interventions
Group B: Active surveillance0 interventions

Trial outcomes

Primary outcomes

1

Incidence of breast cancer following RRM

The primary outcome of interest is the incidence of breast cancer following RRM, defined as a histologically confirmed diagnosis of in situ or invasive breast cancer present within the nipple/areola, skin, subcutaneous tissue of the chest wall/reconstructed breast, or axillary lymph nodes. Patients with clinically occult invasive breast cancer diagnosed at the time of RRM (ie. on mastectomy pathology) will be excluded from the primary outcome analysis.

Time frame
10 years

Secondary outcomes

1

Incidence of RRM

To evaluate uptake of RRM versus active surveillance amongst an international cohort of unaffected women with high-penetrance GPVs in BRCA1/2, PALB2, CDH1, PTEN, or TP53

Time frame
10 years
2

Incidence of post-operative complications

To evaluate post-operative complications and supplemental surgery following NSM, SSM, and total mastectomy in those undergoing RRM

Time frame
10 years
3

Incidence of pathologic outcomes following NSM

To evaluate pathologic outcomes following RRM, including the presence of high-risk lesions or occult in situ and/or invasive malignancy

Time frame
10 years
4

Number of participants using endocrine prevention

To explore the use of endocrine prevention in unaffected women with high-penetrance GPVs in BRCA1/2, PALB2, CDH1, PTEN, or TP53 who elect to undergo active surveillance

Time frame
10 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Sir Mortimer B. Davis - Jewish General Hospital

Lead sponsor

Cancer Research Society

Collaborator

Quebec Breast Cancer Foundation

Collaborator