Prerandomization surgical training for the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-32 trial - A randomized phase III clinical trial to compare sentinel node resection to conventional axillary dissection in clinically node-negative breast cancer

被引:74
作者
Harlow, SP
Krag, DN
Julian, TB
Ashikaga, T
Weaver, DL
Feldman, SA
Klimberg, VS
Kusminsky, R
Moffat, FL
Noyes, RD
Beitsch, PD
机构
[1] Univ Vermont, Coll Med, Dept Surg, Burlington, VT 05405 USA
[2] Univ Vermont, Coll Med, Dept Biometry, Burlington, VT 05405 USA
[3] Univ Vermont, Coll Med, Dept Pathol, Burlington, VT 05405 USA
[4] Vermont Canc Ctr, Burlington, VT USA
[5] Allegheny Gen Hosp, Dept Surg, Pittsburgh, PA 15212 USA
[6] St Paul Hosp, Dept Surg, Dallas, TX USA
[7] Beth Israel Deaconess Med Ctr, Dept Surg, New York, NY 10003 USA
[8] Dept Surg, Little Rock, AR USA
[9] Arkansas Canc Res Ctr, Little Rock, AR USA
[10] Charleston Area Med Ctr, Dept Surg, Charleston, WV USA
[11] Univ Miami, Dept Surg, Miami, FL 33152 USA
[12] Sylvester Canc Ctr, Miami, FL USA
[13] LDS Hosp, Dept Surg, Salt Lake City, UT USA
关键词
D O I
10.1097/01.sla.0000149429.39656.94
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective: To train surgeons in a standardized technique of sentinel lymph node biopsy and to prepare them for the requirements of a prospective randomized surgical trial. Summary Background Data: The NSABP B32 trial opened to accrual in May 1999. A significant component of this trial was a prerandomization training phase of surgeons performed by a group of core surgical trainers. The goals of this training phase were to expeditiously instruct surgeons in a standardized technique of sentinel lymph node biopsy and to educate those same surgeons in complete and accurate data collection and source documentation for the trial. Methods: This study is a description of the training data collected in a prospective fashion for the training component for surgeon entry into the B32 trial, evaluating the effectiveness of the training program in regards to surgical outcomes and protocol compliance. Results: Two hundred twenty-six registered surgeons underwent site visit training by a core surgical trainer and 187 completed training and were approved to randomize patients on the trial. The results of 815 training (nontrial) cases demonstrated a technical success rate for identifying sentinel nodes at 96.2% with a false negative rate of 6.7%. A protocol compliance analysis, which included the evaluation of 94 separate fields, showed mean protocol compliance of 98.6% for procedural fields, 95.5% for source documentation fields and 95.0% for data entry fields. Conclusions: This training and quality control program has resulted in a large number of surgeons capable of performing sentinel lymph node biopsy in a standardized fashion with a high degree of protocol compliance and pathologic accuracy. This will ensure optimal results for procedures performed on the randomized phase of the trial.
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页码:48 / 54
页数:7
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