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CTRI Number  CTRI/2020/04/024578 [Registered on: 13/04/2020] Trial Registered Prospectively
Last Modified On: 01/04/2020
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Other (Specify) [Intraoperative ultrasound]  
Study Design  Single Arm Study 
Public Title of Study   The use of ultrasound in detecting and guiding non-palpable tumor resection in breast conservation surgery after chemotherapy: A pilot study  
Scientific Title of Study   Role of intraoperative ultrasound in breast conservation surgery for non-palpable residual disease after neoadjuvant chemotherapy: A Prospective pilot study  
Trial Acronym   
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Paul Augustine 
Designation  Additional Professor 
Affiliation  Regional Cancer Centre 
Address  Department of Surgical Oncology, Regional Cancer Centre

Thiruvananthapuram
KERALA
695011
India 
Phone  9447220035  
Fax    
Email  augustpaul@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Vijayasarathy S  
Designation  MCh Surgical resident  
Affiliation  Regional Cancer Centre, Trivandrum  
Address  Department of Surgical Oncology, Regional Cancer Centre

Thiruvananthapuram
KERALA
695011
India 
Phone  9176618802  
Fax    
Email  vijayasarathy1988@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Vijayasarathy S  
Designation  MCh Surgical resident  
Affiliation  Regional Cancer Centre, Trivandrum  
Address  Department of Surgical Oncology, Regional Cancer Centre


KERALA
695011
India 
Phone  9176618802  
Fax    
Email  vijayasarathy1988@gmail.com  
 
Source of Monetary or Material Support  
Regional Cancer Centre, Thiruvananthapuram 
 
Primary Sponsor  
Name  Regional Cancer Centre 
Address  Thiruvananthapuram 
Type of Sponsor  Research institution and hospital 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Vijayasarathy S  Regional Cancer Centre  Division of Surgical Oncology
Thiruvananthapuram
KERALA 
9176618802

vijayasarathy1988@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Human Ethics Committee  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: C50-C50||Malignant neoplasms of breast,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Intraoperative ultrasound  use of ultrasound during breast conserving surgery for margins  
Comparator Agent  Palpatory method  Use of palpation for assessment of margins during breast conserving surgery 
 
Inclusion Criteria  
Age From  25.00 Year(s)
Age To  75.00 Year(s)
Gender  Female 
Details  All patients with non-palpable residual lesion(radiologically detected) after NACT in breast cancer undergoing BCS in RCC, Trivandrum

 
 
ExclusionCriteria 
Details   
 
Method of Generating Random Sequence   Not Applicable 
Method of Concealment   Not Applicable 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
To compare adequacy of margin status by intraoperative ultrasound with frozen section analysis and final histopathology report  1 month after surgery 
 
Secondary Outcome  
Outcome  TimePoints 
To determine the rate of margin positivity and re-excision
To assess the impact of IOUS on resection volumes and cosmetic outcome
 
1 month after surgery 
 
Target Sample Size   Total Sample Size="30"
Sample Size from India="30" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   15/04/2020 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="0"
Months="10"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   NIL 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Brief Summary  

Complete clinical response after neoadjuvant chemotherapy (NACT) in breast cancer makes localization of residual lesion challenging. This may lead to margin positivity and excess resection volumes in breast conserving surgery (BCS). Subsequently the cosmetic outcome is also affected. Currently there is no standard method for the preoperative localization or the amount of breast tissue to be resected in BCS. Recent literature has stated that intraoperative ultrasound (IOUS) gives good results in terms of localization of residual lesion, reducing re-excision rates, facilitating minimal breast tissue resection and better cosmetic outcome. 



Aim


To study the feasibility of intraoperative ultrasound in localization of non-palpable residual lesion(radiologically detected) in BCS after NACT and evaluate the efficiency of the procedure



Objectives

Primary:   

  1. To compare adequacy of margin status by IOUS with frozen section analysis and final histopathology report

Secondary

  1. To determine the rate of margin positivity and re-excision 

  2. To assess the impact of IOUS on resection volumes and cosmetic outcome 



Methodology

Study type-  Prospective

Study setting-  Regional Cancer Centre, Trivandrum

Study population-  Patients with non-palpable residual lesion(radiologically detected) after NACT in breast cancer undergoing BCS in RCC, Trivandrum

Sample size- 30


Inclusion criteria 

All patients with non-palpable residual lesion(radiologically detected) after NACT in breast cancer undergoing BCS in RCC, Trivandrum


Exclusion criteria

  1. Multiple residual lesions

  2. Patients with previous surgery of affected breast 



Technique


The marking of skin projection of residual lesion, measurement of size and distance of lesion from skin(mm) is done by the sonologist just prior to surgery. On table, breast tissue is held in uniform position throughout the procedure by hand. Linear array transducer probe covered with a sterile  glove that enables it to be used in the surgical field) is positioned and residual lesion is localised. A guide wire or needle is inserted into the residual lesion. Lesion size, lesion-to-skin distance and the lesion-to-pectoral fascia distance are measured in millimeters.

After making the incision, the skin flap is raised with the goal of obtaining 1 cm margin of healthy breast tissue around the tumour. Tumor resection margins marked using blue dye over breast tissue by insulin syringe and extent of dissection is guided by repeated use of ultrasound from different angles. The location and depth of the lesion will be continuously monitored to ensure the maintenance of adequate resection margins. Subsequently, a spherical lump of breast tissue excised with the desired 1 cm margin. If tumour location does not permit a clear 1 cm deep margin, pectoralis major fascia is taken. The wound bed is examined by ultrasound for residual lesion. The excised specimen is examined by ultrasound to  confirm adequate margins. If the margin appeared less than 1cm desired margin, additional breast tissue is resected in that direction. The specimen will be subjected to frozen section analysis and the margin status will be compared. 


Post procedure


All patients will undergo axillary dissection. According to the final histopathology report, patient will receive adjuvant treatment as per standard protocol.



Calculation of Volumes and Resection Ratio

Parameters

1. Tumor diameter 

2. Three dimensions of the surgical specimen

Volumes

1.TV(tumor volume)

2.ORV(optimal resection volume)

3.TRV(total resection volume). 


  • Tumor is defined as sphere. The diameter of the tumor (pT) corresponds to largest distance(in cm) between points on lesion margin. 

TV = 4/3 p r3

p=3.14

  • ORV is defined as spherical volume of tumor with an added 1.0 cm margin of healthy breast tissue

ORV = 4/3 p (r + 1.0 cm)3

  • TRV represents volume of surgical specimen  defined as an ellipsoid. The three dimensions of the surgical specimen (in cm), as measured by the pathologist.

TRV = 4/3 p abc 

a, b, and c representing half of each of the three dimensions of surgical specimen

  • ERV represents the excess resection volume obtained by calculating the difference between total and optimal resection volumes.

ERV = TRV-ORV

  • CRR represents the calculated resection ratio

CRR = TRV/ORV


If re-excision is performed, the re-excision volumes(4/3p(r)3) will be calculated and TRV will be the sum of resection volumes. In a perfect excision, TRV = ORV and CRR= 1.0. If TRV is twice the size of ORV, then CRR will be  2.0.


Margin status


If no residual cancer cells are found at resection margin, margin will be considered negative. For negative margins, the distance to the nearest margin(mm) will be noted. Margins will be considered positive when cancer cells are microscopically present at resection margin.


Cosmesis assessment


Patient will be followed up as per standard protocol for breast cancer. Cosmesis will be assessed at one month by patient and treating surgeon team independently. Patients will rate cosmesis using visual analogue scale as not satisfied, satisfied or extremely satisfied. Surgeon team will rate as acceptable, good or excellent. 


 
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