This randomized controlled trial is to evaluate the impact of additional cavity shaving (CS) on pathological cavity margin (CM) status in breast cancer patients. Patients receiving standard breast-conserving surgery (BCS) will be randomized to intra-operative CM assessment versus intra-operative CS followed by CM assessment. The primary objective of this study is to assess the impact of CS on intra-operative CM status, intra-operative re-excision rate, post-operative CM status and re-excision rate, cosmetic outcomes, and on intraoperative time and medical costs.
After stratified and blocked randomization, the patients' name, admission ID and treatment assignment will be written on a slip of paper, and will be placed in a sealed envelop. A label with the patients' name and admission ID will be placed on the sealed envelop, which will be kept in a locked file. On the day of surgery, a research coordinator will bring the sealed envelope to the operation room. During the standard-of-care BCS, the tumor was excised with a rim of grossly normal tissue. Additional resections are allowed when any of the margins of the tumor-containing specimen were suspected to be inadequate on the basis of standard gross evaluation by surgeons. Prior to intra-operative CM assessment, the research co-ordinator will unseal the envelop and determine which procedure has been designated to the patient. The cosmetic outcome and the quality of life will be evaluated at the day of discharge, after completion of radiotherapy and one year by the patient herself, her partner and a research co-ordinator.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
181
Resect the residual cavity circumferentially (superior, inferior, medial, lateral) and the thickness of the cavity shaving depends on the surgeon's discretion (Recommended 0.5-1.0cm). The principles of the cavity shaving includes: 1) do not compromise the cosmetic outcomes; 2) covers the entire cavity;
For standardized BCS(Chen K, et al. Ann Surg Oncol. 2012), we resect a rim of 1 cm macroscopically normal tissue around the tumor. The anterior and posterior margins of the tumor-containing specimen extended up to the subdermal plane of the skin and down to the pectoralis major fascia, respectively. The anterior and posterior CMs assessment will not be needed. A surgical blade was used for resecting the CMs (superior, inferior, medial and lateral) to render the thickness of the CMs as thin as possible. No procedures were required for distinguishing the inner and outer surface. They were then frozen and cut parallel, but not perpendicular to the largest surface area. CMs were defined as positive when in situ or invasive carcinoma was found intraoperatively by frozen-section analysis.
Sun-Yat-Sen Memorial Hospital of Sun-Yat-Sen University
Guangzhou, Guangdong, China
Positivity rate of CMs by intraoperative frozen section analysis.
Proportion of patients with at least one positive(invasive carcinoma or carcinoma in situ, excluding LCIS) CMs on intraoperative frozen section analysis
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Intra-operative rate of suspected/positive CM
Proportion of patients with at least one positive(invasive carcinoma or carcinoma in situ, excluding LCIS) or suspected CMs on intraoperative frozen section analysis. Suspected CMs were defined as CMs with severe atypical hyperplasia observed by frozen section analysis.
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Rate of intra-operative re-excision for suspected/positive CMs
For patients with positive CMs, intra-operative re-excision was required. For patients with suspected CMs,intra-operative re-excision is left to the surgeon's discretion
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Rate of a second-time surgery for post-operative positive CMs
Positive CMs by post-operative pathological analysis may require a second-time surgery for re-excision.
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Proportion of patients successfully undergone BCT
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Cost-effectiveness of cavity shaving in BCS as measured by operative time of the surgery
Surgery time(start from making the incision to closure) will be analyzed.
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Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Cost-effectiveness of cavity shaving in BCS as measured by medical cost of the surgery
Medical costs will be analyzed.
Time frame: Completion of surgery for all enrolled patients (approximately 12 months)
Cosmetic outcome
Patients', partners' and physicians' perceptions of the cosmetic outcomes as measured by Harvard/NSABP/RTOG criteria
Time frame: One year after surgery.
Adverse events
Time frame: One year after surgery.
Quality of life.
Chinese version of validated QLQ-C30 and QLQ-BR23 questionnaire
Time frame: One year after surgery.