Outcomes of Breast Conservative Surgery for Post Chemotherapy Tumour Size After Response to Neoadjuvant Chemotherapy
NCT ID: NCT05115279
Last Updated: 2021-11-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
1 participants
INTERVENTIONAL
2021-06-01
2024-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Complete pathological response after neoadjuvant systemic treatment is high, while complete clinical response rates are even higher. Because it is difficult to localize the original tumor bed after a complete clinical and radiological response, marking the tumor before the start of neoadjuvant systemic treatment is required to enable breast-conserving surgery afterward. Achieving adequate margins of excision is an important component of breast surgery. Local recurrence rates are significantly higher for patients who have positive margins of excision (9) some prospective and retrospective data suggested that patients with BCT after neoadjuvant therapy may have an increased risk for the development of a local recurrence .
If this were true, there would be no further advantage of neoadjuvant therapy and this treatment option could be questioned altogether.
A common question raised with respect to performing breast-conserving therapy after neoadjuvant chemotherapy is the volume of breast tissue that should be resected
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1. Inclusion criteria:
1. Female patients with operable breast cancer
2. Female Patient aged from 20 to 60 years old
3. Patients who are fit for general anesthesia.
4. Patients who provide a written informed consent.
5. Patient who agree to provide short term outcome data and agree to provide contact information to provide contact information.
2. Exclusion criteria:
1. Female patients less than 20 years old
2. Stage 4 breast cancer
3. Patient has no pathological or clinical response to NACT
4. Patients who are contraindicated for radiotherapy
5. Pregnant patients in first trimester
6. Patient with inflammatory carcinoma
3. Sample Size Calculation:
Prospective trial study include 50 patient whom fulfilled the inclusion criteria 2.4.4 -Study tools (in detail, e.g., lab methods, instruments, steps, chemicals, …): This prospective study is including patients will be diagnosed breast cancer and will receive neoadjuvant chemotherapy .
All patients underwent a preoperative clinical evaluation including physical examination (PE), ultrasonography, mammograph and MRI then biopsies of the breast tumor were performed to determine the histological subtype and receptor status Methods
Pro-operative preparation:
After confirming diagnosis of breast cancer and its molecular type patient undergoing marking the tumor and axillary lymph nodes by clips before receiving neoadjuvant chemotherapy.
Making Virtual pre-operative breast conserving surgical technique based on the previous tumor size
The Surgical steps:
* Depending on new tumor size ,site of the tumor ,breast cup size and degree of breast ptosis ;oncoplastic breast conserving technique would be selected
* A prophylactic antibiotic as first generation cephalosporin is given intravenous.
* Skin preparation by povidine iodine.
* Excision of the mass with safety margin.
* Sentinel axillary lymph node or complete axillary clearance depend on axillary lymph node status
* All specimens were oriented with sutures
* A frozen section examination of the specimen was performed intraoperative
* When the margin status was inadequate, a re-excision was performed
* Closure as drawn by different oncoplastic technique
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Breast conservative Surgury after neuadjvant chemotherapy
Breast conservative Surgury
breast conservative surgery for post chemotherapy tumour size
* Skin preparation by povidine iodine.
* Excision of the mass with safety margin.
* Sentinel axillary lymph node or complete axillary clearance depend on axillary lymph node status
* All specimens were oriented with sutures
* A frozen section examination of the specimen was performed intraoperative
* When the margin status was inadequate, a re-excision was performed
* Closure as drawn by different oncoplastic technique
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
breast conservative surgery for post chemotherapy tumour size
* Skin preparation by povidine iodine.
* Excision of the mass with safety margin.
* Sentinel axillary lymph node or complete axillary clearance depend on axillary lymph node status
* All specimens were oriented with sutures
* A frozen section examination of the specimen was performed intraoperative
* When the margin status was inadequate, a re-excision was performed
* Closure as drawn by different oncoplastic technique
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Female Patient aged from 20 to 60 years old
3. Patients who are fit for general anesthesia.
4. Patients who provide a written informed consent.
5. Patient who agree to provide short term outcome data and agree to provide contact information to provide contact information.
Exclusion Criteria
1. Female patients less than 20 years old
2. Stage 4 breast cancer
3. Patient has no pathological or clinical response to NACT
4. Patients who are contraindicated for radiotherapy
5. Pregnant patients in first trimester
6. Patient with inflammatory carcinoma
20 Years
60 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Assiut University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
samir hosny mahmoud
breast surgeon
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Assuit university
Asyut, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Assuit
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
assuitu faculty of medicine
Identifier Type: -
Identifier Source: org_study_id