Areola Preservation in NSM With Nipple Involvement

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

Background:

During nipple-sparing mastectomy (a surgery that removes breast tissue but keeps the nipple and areola), doctors test the tissue behind the nipple right away. If cancer cells are found in this nipple tissue, current guidelines say the entire nipple and areola must be removed. However, research suggests that when the nipple is involved, the surrounding pigmented skin (the areola) is very rarely affected by cancer. Removing it might be unnecessary and leads to a worse cosmetic outcome, which can impact a woman's self-image and quality of life. Currently, there is no prospective study to guide whether the areola can be safely preserved in this specific situation.

Purpose:

This is a pilot study that aims to explore the feasibility, safety, and early outcomes of a new surgical procedure: preserving the areola and performing immediate nipple reconstruction when cancer is found in the nipple during surgery.

Study Plan:

This is a single-arm, single-center, prospective, exploratory study. Women with early-stage breast cancer who are scheduled for a nipple-sparing mastectomy will be invited. Only if cancer is confirmed in the nipple during their surgery will they be enrolled into the single test group. In this group:

The nipple is removed.

A small ring of tissue from under the areola is tested immediately (second frozen section). If this ring shows no cancer, the areola skin is preserved.

A new nipple is created during the same operation using a local skin flap technique (purse-string suture).

All patients will have immediate breast reconstruction.

We plan to include about 40-60 patients at one hospital. Patients will be closely followed for 3 years with regular check-ups and scans to monitor for any cancer recurrence or complications.

What We Will Measure (Exploratory Endpoints):

Safety \& Feasibility: The success rate of areola preservation (based on negative second frozen section), surgical complication rates (e.g., infection, tissue necrosis).

Early Effectiveness: The rate of cancer returning in the breast/chest wall area within 3 years (local recurrence).

Patient-Reported Outcomes: Patient satisfaction with their breasts and well-being, measured by the BREAST-Q questionnaire before and after surgery.

Why This Study is Important:

This is the first prospective study to systematically evaluate this new surgical approach. The results will provide crucial preliminary data on safety and early outcomes. If the findings are promising, they will form the foundation for designing a larger, controlled trial in the future. Ultimately, this research could lead to a new option that offers women better cosmetic results and improved quality of life after mastectomy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female, age ≥ 18 years.

Pathologically confirmed primary invasive breast carcinoma or ductal carcinoma in situ (DCIS).

Clinical tumor stage cTis-2, N0-2, M0 (AJCC 8th Edition).

Planned for therapeutic nipple-sparing mastectomy (NSM) with immediate reconstruction.

Disqualifiers

Clinical or radiological suspicion of areola or skin involvement.

Inflammatory breast cancer.

Pregnancy or lactation.

Any severe medical or psychiatric condition that, in the investigator's judgment, would preclude safe participation or compliance.

Trial design

Design model

Single group

Treatments tested in this trial

  • Areola-Preserving Nipple-Sparing Mastectomy with Immediate Nipple Reconstruction

    Procedure/Surgery

    This is a combined surgical procedure for patients with intraoperative nipple involvement during nipple-sparing mastectomy. After resection of the involved nipple, a full-thickness peri-areolar tissue margin is harvested for a second intraoperative frozen section. If the margin is negative for carcinoma, the areola skin is preserved. An immediate nipple reconstruction is then performed using a local skin flap technique (e.g., purse-string suture). This is followed by standard immediate breast reconstruction (implant-based or autologous).

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Areola Preservation & Nipple Reconstruction GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Local Recurrence Rate

The incidence of local recurrence in the ipsilateral chest wall/skin or residual breast tissue, assessed by clinical examination and imaging (breast ultrasound and/or MRI), with pathological confirmation for suspected cases.

Time frame
3 years post-surgery

Secondary outcomes

1

Rate of Successful Areola Preservation

The proportion of patients in whom the areola is successfully preserved, defined as having a negative result on the second intraoperative frozen section of the peri-areolar margin.

Time frame
Intraoperative
2

Incidence of Postoperative Complications

The rate of surgical complications, including but not limited to areolar skin necrosis (partial/full), infection, seroma, hematoma, and implant loss/failure.

Time frame
Within 90 days post-surgery
3

Change in Patient-Reported Satisfaction and Well-being

Change in scores from baseline as measured by the validated BREAST-Q questionnaire modules (Satisfaction with Breasts, Psychosocial, Sexual, and Physical Well-being).

Time frame
Baseline, 6, 12, 24, and 36 months post-surgery

Other outcomes

Sponsors and contacts

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