Eliminating Breast Surgery for Invasive Cancer with Exceptional Response to Neoadjuvant Systemic Therapy: Prospective Multicenter Clinical Trial Planned Initial Feasibility Endpoint

被引:8
作者
Johnson, Helen M. [1 ]
Valero, Vicente [2 ]
Yang, Wei T. [3 ]
Smith, Benjamin D. [4 ]
Krishnamurthy, Savitri [5 ]
Shen, Yu [6 ]
Lin, Heather [6 ]
Lucci, Anthony [1 ]
Rauch, Gaiane M. [3 ,7 ]
Kuerer, Henry M. [1 ,8 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Breast Surg Oncol, Houston, TX USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Breast Imaging, Houston, TX USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Radiat Oncol, Houston, TX USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX USA
[7] Univ Texas MD Anderson Canc Ctr, Dept Abdominal Imaging, Houston, TX USA
[8] Univ Texas MD Anderson Canc Ctr, Breast Programs MD Anderson Canc Network, 1515 Holcombe Blvd,Unit 1434, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
TRASTUZUMAB; EFFICACY;
D O I
10.1097/XCS.0000000000000670
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: Response to neoadjuvant systemic therapy (NST) for breast cancer enables tailoring of subsequent therapy. Image-guided breast biopsy after NST can accurately predict a pathologic complete response (pCR). The feasibility phase of the clinical trial reported here assesses omission of breast surgery followed by radiotherapy in terms of local recurrence before trial expansion. STUDY DESIGN: Women with unicentric, cT1-2 N0-1 M0 triple-negative (TNBC) or human epidermal growth factor receptor 2-positive breast cancer (HER2+BC) cancer with <2 cm residual disease on post-NST imaging were eligible to enroll. If no residual invasive or in situ disease was identified by image-guided, vacuum-assisted core biopsy (VACB), breast surgery was omitted, and radiotherapy delivered. The primary endpoint for the feasibility phase was ipsilateral breast tumor recurrence at 6 months. If any recurrence occurred during the feasibility phase the trial would halt. RESULTS: Thirteen patients were enrolled from March 2017 to October 2018. The mean age was 60.8 years (range 51 to 75) and most patients were White (69.2%) and non-Hispanic/Latino (84.6%). All patients had invasive ductal carcinoma (6 TNBC, 7 HER2+BC). Mean tumor size was 2.4 cm (range 0.9 to 5.0) before NST and 0.7 cm (range 0 to 1.8) after NST. Seven patients (53.8%) had residual disease identified on VACB; the remaining 6 (46.2%) comprised the feasibility cohort. At a median follow-up of 44.3 months (range 41.3 to 51.3) there was no ipsilateral breast tumor recurrence in this cohort. CONCLUSIONS: These early data suggest that omission of breast surgery in patients with invasive TNBC and HER2+BC with no evidence of residual disease on standardized VACB after NST is potentially feasible. Results from the expansion phase of this clinical trial will be reported per protocol prespecified analyses. (J Am Coll Surg 2023;237:101-108. (c) 2023 by the American College of Surgeons. Published by Wolters Kluwer Health, Inc. All rights reserved.)
引用
收藏
页码:101 / 108
页数:8
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