Skip to main content
OpenTrials
Recruiting

NCT Number: NCT03417622

Wide Margin vs. Narrow Margin in Postneoadjuvant Lumpectomy

Breast cancer patients often receive systemic drugs as the initial curative treatment of their disease. The initial systemic therapy leads to a variable degree of tumor shrinkage. At present, there is no evidence-based consensus among breast surgeons on the optimal extent of resection after considerable tumor shrinkage and whether resection margin should be designed according to the tumor extent before treatment or the extent after treatment. This trial will help determine the optimal extent of resection in tumors that exhibits a significant change in volume after primary systemic therapy.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Mansoura University Oncology Center

Al Mansurah, DK, 35516, Egypt

Location status: Recruiting

Location contact

Aiman El-Saed, MD,PhD

SUB_INVESTIGATOR

Maha El-Zaafarany, MD

SUB_INVESTIGATOR

Osama Hussein, MD,PhD,FEBS

CONTACT

[email protected]

+2010 9981 5110

About this study

Primary systemic (neoadjuvant) therapy (NAT) is a widely practised curative treatment for invasive breast cancer. Neoadjuvant chemotherapy (before surgery) and adjuvant chemotherapy (after surgery) had equivalent survival rates in major randomized trials. In these studies, preoperative systemic therapy increased the patient's chance to achieve breast conservation. The down side was a clear trend towards increased ipsilateral breast tumor recurrence. Preoperative chemotherapy leads to patchy, irregular cell death known as honeycomb effect and thus may lead to a misleading false negative resection margin of a tumorectomy operation. Even with the advent of oncoplastic techniques which allowed larger resection volumes with satisfactory cosmetic results, rates of re-excision, mastectomy and local relapse did not differ from those after traditional lumpectomy operations. As of today, there is no consensus -based on evidence- on the optimal width of margin in patients who are offered breast conservative surgery (BCS) after systemic therapy. In view of the current uncertainty and lack of evidence, The present trial is designed to answer the following question (Specific aim): Does planning the resection margin according to the pre-treatment tumor extent improve the local recurrence rate in patients receiving breast conservative surgery after systemic therapy?

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Biopsy-proven diagnosis of invasive adenocarcinoma of the breast.
  • Tumor stage T 1-4b
  • Nodal stage N 0-2
  • ASA (American Society of Anesthesiologists) class I-II

Exclusion criteria

  • Patients opting for mastectomy.
  • Patients advised for mastectomy by the treating physician.
  • Patients opting for primary surgical treatment.
  • Patients advised for primary surgical treatment by the treating physician.
  • Metastatic patients.
  • Multifocal tumors.
  • Lobular neoplasia.
  • Current pregnancy or pregnancy less than 6 months from the enrollment date.
  • Active second cancer.

Treatment and study plan

Bracketing

Procedure

At the beginning of therapy, ultrasonographic examination is used to measure the tumor in three dimensions and bracket the tumor using 4-6 metal clips which will serve as markers for the initial tumor extent in case of tumor shrinkage in response to systemic treatment.

neoadjuvant therapy

Drug

All patients will receive primary systemic therapy according to the current institutional guidelines. Drugs include cytotoxic chemotherapy, hormonal therapy and/or anti-HER2/neu therapy as indicated.

Post-treatment volume margin resection

Procedure

The lumpectomy resection margin is planned according to the identifiable tumor at operation. The initial extent of the tumor at diagnosis is not taken in account. If there is complete clinical response to systemic therapy (i.e. no identifiable tumor), the center of the bracketed tissue is biopsied.

Pre-treatment volume margin resection

Procedure

The lumpectomy includes the whole bracketed tissue to take in account the initial tumor extent before systemic therapy.

Primary outcomes

  1. Local recurrence rate.

    Time frame: at 60 months after the date of diagnosis.

    The rate of local recurrence at five years.

Secondary outcomes

  1. Local disease-free survival.

    Time frame: up to 60 months from the date of diagnosis.

    The proportion of patients who remain free of local disease recurrence.

  2. Disease-free survival.

    Time frame: up to 60 months from the date of diagnosis.

    The proportion of patients who remain free of disease recurrence.

  3. Overall survival.

    Time frame: up to 60 months from the date of diagnosis.

    The proportion of patients who are alive.

Other outcomes

  1. Mastectomy rate.

    Time frame: at 6 months from the date of first surgical intervention.

    The proportion of patients who undergo mastectomy after failed conservative surgery.

  2. Cosmetic score.

    Time frame: at 6 months from the date of first surgical intervention.

    Numeric score description of the cosmetic outcome of breast conservative surgery.

Study contacts

Contact information is provided by the study sponsor or research team.

Osama Hussein, MD,PhD,FEBS

CONTACT

[email protected]

+2010 9981 5110

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Surgical Resection Margin According to the Post-treatment Tumor Volume Versus the Pre-treatment Tumor Volume in Breast Conservative Surgery for Invasive Breast Cancer Patients Receiving Primary Systemic Therapy: Randomized Controlled Trial

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Jan 31, 2018
Registry last updated
Feb 25, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.