Wide Margin vs. Narrow Margin in Postneoadjuvant Lumpectomy

Sponsor
Mansoura University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03417622
Collaborator
(none)
370
1
2
84
4.4

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Bracketing
  • Drug: Neoadjuvant therapy
  • Procedure: Post-treatment volume margin resection
  • Procedure: Pre-treatment volume margin resection
Phase 3

Detailed Description

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?

Study Design

Study Type:
Interventional
Anticipated Enrollment :
370 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official 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
Actual Study Start Date :
Aug 1, 2019
Anticipated Primary Completion Date :
Aug 1, 2026
Anticipated Study Completion Date :
Aug 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Post-treatment volume-resection margin

Lumpectomy is performed with resection margin of the clinically / radiologically identifiable post-treatment tumor.

Procedure: Bracketing
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.

Drug: Neoadjuvant therapy
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.

Procedure: Post-treatment volume margin resection
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.

Active Comparator: Pre-treatment volume-resection margin

Lumpectomy is performed with resection margin of the bracketed tissue.

Procedure: Bracketing
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.

Drug: Neoadjuvant therapy
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.

Procedure: Pre-treatment volume margin resection
The lumpectomy includes the whole bracketed tissue to take in account the initial tumor extent before systemic therapy.

Outcome Measures

Primary Outcome Measures

  1. Local recurrence rate. [at 60 months after the date of diagnosis.]

    The rate of local recurrence at five years.

Secondary Outcome Measures

  1. Local disease-free survival. [up to 60 months from the date of diagnosis.]

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

  2. Disease-free survival. [up to 60 months from the date of diagnosis.]

    The proportion of patients who remain free of disease recurrence.

  3. Overall survival. [up to 60 months from the date of diagnosis.]

    The proportion of patients who are alive.

Other Outcome Measures

  1. Mastectomy rate. [at 6 months from the date of first surgical intervention.]

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

  2. Cosmetic score. [at 6 months from the date of first surgical intervention.]

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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mansoura University Oncology Center Mansourah DK Egypt 35516

Sponsors and Collaborators

  • Mansoura University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Osama Hussein, Professor of surgery (surgical oncology), Mansoura University
ClinicalTrials.gov Identifier:
NCT03417622
Other Study ID Numbers:
  • R.18.02.33
First Posted:
Jan 31, 2018
Last Update Posted:
Feb 25, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Osama Hussein, Professor of surgery (surgical oncology), Mansoura University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 25, 2021