Impact of neoadjuvant chemotherapy and pathological complete response on eligibility for breast-conserving surgery in patients with early breast cancer: A meta-analysis

被引:38
作者
Criscitiello, Carmen [1 ]
Golshan, Mehra [2 ,3 ,4 ]
Barry, William T. [4 ]
Viale, Giulia [1 ,5 ]
Wong, Stephanie [2 ,3 ]
Santangelo, Michele [4 ]
Curigliano, Giuseppe [1 ,5 ]
机构
[1] European Inst Oncol, Div New Drug Dev, Milan, Italy
[2] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Univ Federico II, Dept Adv Biomed Sci, Gen Surg, Naples, Italy
[5] Univ Milan, Dept Oncol & Hematooncol, Milan, Italy
关键词
Neoadjuvant therapy; Breast cancer; Mastectomy; Quadrantectomy; SURGICAL ADJUVANT BREAST; INDUCTION CHEMOTHERAPY; OPEN-LABEL; RANDOMIZED-TRIAL; SYSTEMIC THERAPY; CONSERVATION; TRASTUZUMAB; MULTICENTER; PERTUZUMAB; LAPATINIB;
D O I
10.1016/j.ejca.2018.03.023
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We conducted a meta-analysis of randomised trials evaluating pathological complete response (pCR) and surgical outcomes after neoadjuvant systemic therapy (NST) in patients with early breast cancer (EBC). Patients and methods: The primary outcome was breast-conserving surgery (BCT) rate. Secondary outcomes were pCR rate and association to BCT. Meta-analyses were performed using random effects models that use inverse-variance weighting for each treatment arm based on evaluable patients. Point estimates are reported with 95% confidence interval (CI), and p < 0.05 was considered statistically significant. Results: Thirty-six studies were identified (N = 12,311 patients). We selected for the analysis 16 of 36 studies reporting both pCR and BCT for at least one treatment arm. Arms per study ranged from one to six; 42 independent units were available to evaluate the association between pCR and BCT. BCT rate ranged 5-76% across arms with an average BCT of 57% (95% CI 52-62%). Significant heterogeneity was observed among the trials (Cochrane Q = 787, p < 0.001, I-2 = 97%). In the meta-regression model, BCT rates were not significantly associated with year of first patient-in (p = 0.89), grade (p = 0.93) and hormonereceptor status (p = 0.39). Clinical N-stage (p = 0.01) and human epidermal growth factor receptor (HER2) status (p = 0.03) were significantly associated with BCT. pCR rate ranged 3e60% across studies. The average pCR across all study arms was 24% (95% CI 19-29%). No association was observed between pCR rate in a study arm and the resulting BCT rate in a univariate model (p = 0.34) nor after adjusting for HER2 and clinical nodal status (p = 0.82). In the subset of 14 multi-arm studies, no significant association was seen between the differences in pCR and BCT between treatment arms (p = 0.27). Conclusions: pCR does not increase BCT in patients receiving NST for EBC. (C) 2018 Elsevier Ltd. All rights reserved.
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页码:1 / 6
页数:6
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