Eliminating the breast cancer surgery paradigm after neoadjuvant systemic therapy: current evidence and future challenges

被引:128
|
作者
Heil, J. [1 ]
Kuerer, H. M. [2 ]
Pfob, A. [1 ]
Rauch, G. [3 ,4 ,5 ,6 ]
Sinn, H. P. [7 ]
Golatta, M. [1 ]
Liefers, G. J. [8 ]
Peeters, M. J. Vrancken [9 ]
机构
[1] Heidelberg Univ, Breast Unit, Dept Gynaecol, Neuenheimer Feld 440, D-69120 Heidelberg, Germany
[2] Univ Texas MD Anderson Canc Ctr, Dept Breast Surg Oncol, Houston, TX 77030 USA
[3] Charite Univ Hosp Med, Inst Biometry & Clin Epidemiol, Berlin, Germany
[4] Free Univ Berlin, Berlin, Germany
[5] Humboldt Univ, Berlin, Germany
[6] Berlin Inst Hlth, Berlin, Germany
[7] Heidelberg Univ, Dept Pathol, Heidelberg, Germany
[8] Leiden Univ, Med Ctr, Dept Surg, Leiden, Netherlands
[9] Netherlands Canc Inst, Div Surg Oncol, Amsterdam, Netherlands
关键词
breast cancer; individualized treatment; neoadjuvant systemic therapy; oncology; surgery; PATHOLOGICAL COMPLETE RESPONSE; 20-YEAR FOLLOW-UP; CONSERVING THERAPY; CHEMOTHERAPY; NODE; MASTECTOMY; BIOPSY; IDENTIFICATION; METAANALYSIS; MULTICENTER;
D O I
10.1016/j.annonc.2019.10.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In patients with operable early breast cancer, neoadjuvant systemic treatment (NST) is a standard approach. Indications have expanded from downstaging of locally advanced breast cancer to facilitate breast conservation, to in vivo drug-sensitivity testing. The pattern of response to NST is used to tailor systemic and locoregional treatment, that is, to escalate treatment in nonresponders and de-escalate treatment in responders. Here we discuss four questions that guide our current thinking about 'response-adjusted' surgery of the breast after NST. (i) What critical diagnostic outcome measures should be used when analyzing diagnostic tools to identify patients with pathologic complete response (pCR) after NST? (ii) How can we assess response with the least morbidity and best accuracy possible? (iii) What oncological consequences may ensue if we rely on a nonsurgical-generated diagnosis of, for example, minimally invasive biopsy proven pCR, knowing that we may miss minimal residual disease in some cases? (iv) How should we design clinical trials on de-escalation of surgical treatment after NST?
引用
收藏
页码:61 / 71
页数:11
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