[1] HARBECK N,GNANT M.Breast cancer[J].Lancet,2017,389(10074):1134-1150.
[2] BALIC M,THOMSSEN C,WURSTLEIN R,et al.St.Gallen/Vienna 2019:A brief summary of the consensus discussion on the optimal primary breast cancer treatment[J].Breast Care (Basel),2019,14(2):103-110.
[3] LIEDTKE C,JACKISCH C,THILL M,et al.AGO recommendations for the diagnosis and treatment of patients with early breast cancer:Update 2018[J].Breast Care (Basel),2018,13(3):196-208.
[4] Early Breast Cancer Trialists' Collaborative Group (EBCTCG),PETO R,DAVIES C,et al.Comparisons between different polychemotherapy regimens for early breast cancer:meta-analyses of long-term outcome among 100,000 women in 123 randomised trials[J].Lancet,2012,379(9814):432-444.
[5] SMITH LA,CORNELIUS VR,PLUMMER CJ,et al.Cardiotoxicity of anthracycline agents for the treatment of cancer:systematic review and meta-analysis of randomised controlled trials[J].BMC Cancer,2010,29(10):337-337.
[6] EWER MS,LIPPMAN SM.Type II chemotherapy-related cardiac dysfunction:time to recognize a new entity[J].J Clin Oncol,2005,23(13):2900-2902.
[7] SCHNEEWEISS A,CHIA S,HICKISH T,et al.Long-term efficacy analysis of the randomised,phase II TRYPHAENA cardiac safety study:Evaluating pertuzumab and trastuzumab plus standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer[J].Eur J Cancer,2018,89:27-35.
[8] GUENANCIA C,LEFEBVRE A,CARDINALE D,et al.Obesity as a risk factor for anthracyclines and trastuzumab cardiotoxicity in breast cancer:A systematic review and Meta-analysis[J].J Clin Oncol,2016,34(26):3157-3165.
[9] KOTWINSKI P,SMITH G,COOPER J,et al.Body surface area and baseline blood pressure predict subclinical anthracycline cardiotoxicity in women treated for early breast cancer[J].PLoS One,2016,11(12):e0165262-e0165262.
[10] VAN RAMSHORST MS,VAN DER VOORT A,VAN WERKHOVEN ED,et al.Neoadjuvant chemotherapy with or without anthracyclines in the presence of dual HER2 blockade for HER2-positive breast cancer (TRAIN-2):a multicentre,open-label,randomised,phase 3 trial[J].Lancet Oncol,2018,19(12):1630-1640.
[11] TANAKA S,MATSUNAMI N,MORISHIMA H,et al.De-escalated neoadjuvant therapy with nanoparticle albumin-bound paclitaxel and trastuzumab for low-risk pure HER2 breast cancer[J].Cancer Chemother Pharmacol,2019,83(6):1099-1104.
[12] NONE.Adjuvant paclitaxel and trastuzumab for node-negative,HER2-positive breast cancer[J].N Engl J Med,2015,373(20):1989.
[13] PICCART M,PROCTER M,FUMAGALLI D,et al.Interim overall survival analysis of APHINITY (BIG 4-11):a randomized multicenter,double-blind,placebo-controlled[J].Cancer Res,2020,80(01):abstr01-04.
[14] SCHNEEWEISS A,CHIA S,HICKISH T,et al.Pertuzumab plus trastuzumab in combination with standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer:a randomized phase II cardiac safety study (TRYPHAENA)[J].Ann Oncol,2013,24(9):2278-2284.
[15] GIANNI L,PIENKOWSKI T,IM YH,et al.Efficacy and safety of neoadjuvant pertuzumab and trastuzumab in women with locally advanced,inflammatory,or early HER2-positive breast cancer (NeoSphere):a randomised multicentre,open-label,phase 2 trial[J].Lancet Oncol,2012,13(1):25-32.
[16] YU AF,SINGH JC,WANG R,et al.Cardiac safety of dual anti-HER2 therapy in the neoadjuvant setting for treatment of HER2-positive breast cancer[J].Oncologist,2017,22(6):642-647.
[17] VAN RAMSHORST MS,VAN WERKHOVEN E,HONKOOP AH,et al.Toxicity of dual HER2-blockade with pertuzumab added to anthracycline versus non-anthracycline containing chemotherapy as neoadjuvant treatment in HER2-positive breast cancer:The TRAIN-2 study[J].Breast,2016,29:153-159.
[18] NITZ UA,GLUZ O,CHRISTGEN M,et al.De-escalation strategies in HER2-positive early breast cancer (EBC):final analysis of the WSG-ADAPT HER2+/HR- phase II trial:efficacy,safety,and predictive markers for 12 weeks of neoadjuvant dual blockade with trastuzumab and pertuzumab±weekly paclitaxel[J].Ann Oncol,2017,28(11):2768-2772.
[19] GIANNI L,BISAGNI G,COLLEONI M,et al.Neoadjuvant treatment with trastuzumab and pertuzumab plus palbociclib and fulvestrant in HER2-positive,ER-positive breast cancer (NA-PHER2):an exploratory,open-label,phase 2 study[J].Lancet Oncol,2018,19(2):249-256.
[20] GUARNERI V,DIECI MV,BISAGNI G,et al.De-escalated therapy for HR+/HER2+ breast cancer patients with Ki67 response after 2-week letrozole:results of the PerELISA neoadjuvant study[J].Ann Oncol,2019,30(6):921-926.
[21] CORTAZAR P,ZHANG L,UNTCH M,et al.Pathological complete response and long-term clinical benefit in breast cancer:the CTNeoBC pooled analysis[J].Lancet,2014,384(9938):164-172.
[22] NONE.Adjuvant pertuzumab and trastuzumab in early HER2-positive breast cancer[J].N Engl J Med,2017,377(7):702.
[23] VON MINCKWITZ G,HUANG CS,MANO MS,et al.Trastuzumab emtansine for residual invasive HER2-positive breast cancer[J].N Engl J Med,2019,380(7):617-628.
[24] CHAN A,DELALOGE S,HOLMES FA,et al.Neratinib after trastuzumab-based adjuvant therapy in patients with HER2-positive breast cancer (ExteNET):a multicentre,randomised,double-blind,placebo-controlled,phase 3 trial[J].Lancet Oncol,2016,17(3):367-377.
[25] PATHAK M,DWIVEDI SN,DEO S,et al.Effectiveness of added targeted therapies to neoadjuvant chemotherapy for breast cancer:A systematic review and Meta-analysis[J].Clin Breast Cancer,2019,19(6):e690-e700.
[26] WANG BC,FU C,XIE LK,et al.Comparative toxicities of neoadjuvant chemotherapy with or without bevacizumab in HER2-negative breast cancer patients:A Meta-analysis[J].Ann Pharmacother,2020,54(6):517-525.
[27] SCHMID P,CORTES J,PUSZTAI L,et al.Pembrolizumab for early triple-negative breast cancer[J].N Engl J Med,2020,382(9):810-821.
[28] GIANNI L,CS H,EGLE D,et al.Pathologic complete response (pCR) to neoadjuvant treatment with or without atezolizumab in triple negative,early high-riskand locally advanced breast cancer.NeoTRIPaPDL1 Michelangelo randomized study[J].Cancer Res,2020,80(01):abstr03-04.
[29] SELIGER B.231PImmunomonitoring of triple negative breast cancer patients undergoing neoadjuvant therapy (GBG89,Geparnuevo trial)[J].Ann Oncol,2018,29(1):suppl8.
[30] BEAR HD,WAN W,ROBIDOUX A,et al.Using the 21-gene assay from core needle biopsies to choose neoadjuvant therapy for breast cancer:A multicenter trial[J].J Surg Oncol,2017,115(8):917-923.
[31] SAVARIDAS SL,SIM YT,VINNICOMBE SJ,et al.Are baseline ultrasound and mammographic features associated with rates of pathological completes response in patients receiving neoadjuvant chemotherapy for breast cancer[J].Cancer Imaging,2019,19(1):67.
[32] KRIZMANICH-CONNIFF KM,PARAMAGUL C,PATTERSON SK,et al.Triple receptor-negative breast cancer:imaging and clinical characteristics[J].AJR Am J Roentgenol,2012,199(2):458-464.
[33] VAN LA PARRA R,TADROS AB,CHECKA CM,et al.Baseline factors predicting a response to neoadjuvant chemotherapy with implications for non-surgical management of triple-negative breast cancer[J].Br J Surg,2018,105(5):535-543.
[34] SCHEEL JR,KIM E,PARTRIDGE SC,et al.MRI,clinical examination,and mammography for preoperative assessment of residual disease and pathologic complete response after neoadjuvant chemotherapy for breast cancer:ACRIN 6657 trial[J].AJR Am J Roentgenol,2018,210(6):1376-1385.
[35] BASIK M,COSTANTINO J,DE LOS SANTOS J,et al.Phase II trial assessing accuracy of tumor bed biopsies in predicting pathologic response in patients with clinical/radiological complete response after neoadjuvant chemotherapy in order to explore the feasibility of breast-conserving surgery without surgery:NRG Oncology[J].Cancer Res,2019,79(1):abstrOT10901.
[36] HEIL J,PFOB A,H-PP S,et al.Diagnosing residual disease and pathologic complete response after neoadjuvant chemotherapy in breast cancer patients by[J].Cancer Res,2020,80(1):abstr05-03.
[37] BLEICHER RJ.Timing and delays in breast cancer evaluation and treatment[J].Ann Surg Oncol,2018,25(10):2829-2838.
[38] ZHAN QH,FU JQ,FU FM,et al.Survival and time to initiation of adjuvant chemotherapy among breast cancer patients:a systematic review and meta-analysis[J].Oncotarget,2018,9(2):2739-2751.
[39] SULEMAN K,ALMALIK O,HAQUE E,et al.Does the timing of surgery after neoadjuvant therapy in breast cancer patients affect the outcome[J].Oncology,2020,98(3):168-173.
[40] WHITE RL JR,PALMER PP,TRUFAN SJ,et al.Does neoadjuvant chemotherapy for breast cancer affect lymph node harvest rates[J].Am Surg,2019,85(7):690-694.
[41] ROSENBERGER LH,REN Y,THOMAS SM,et al.Axillary lymph node dissection in node-positive breast cancer:are ten nodes adequate and when is enough,enough[J].Breast Cancer Res Treat,2019,179(3):661-670.
[42] ERBES T,ORLOWSKA-VOLK M,ZUR HAUSEN A,et al.Neoadjuvant chemotherapy in breast cancer significantly reduces number of yielded lymph nodes by axillary dissection[J].BMC Cancer,2014,03(14):4.
[43] NGUYEN TT,HOSKIN TL,DAY CN,et al.Decreasing use of axillary dissection in node-positive breast cancer patients treated with neoadjuvant chemotherapy[J].Ann Surg Oncol,2018,25(9):2596-2602.
[44] VON MINCKWITZ G,UNTCH M,BLOHMER JU,et al.Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes[J].J Clin Oncol,2012,30(15):1796-1804.
[45] CAUDLE AS,YANG WT,KRISHNAMURTHY S,et al.Improved axillary evaluation following neoadjuvant therapy for patients with node-positive breast cancer using selective evaluation of clipped nodes:Implementation of targeted axillary dissection[J].J Clin Oncol,2016,34(10):1072-1078.
[46] GIULIANO AE,BALLMAN KV,MCCALL L,et al.Effect of axillary dissection vs no axillary dissection on 10-year overall survival among women with invasive breast cancer and sentinel node metastasis:The ACOSOG Z0011 (alliance) randomized clinical trial[J].JAMA,2017,318(10):918-926.
[47] CHOI J,LAWS A,HU J,et al.Margins in breast-conserving surgery after neoadjuvant therapy[J].Ann Surg Oncol,2018,25(12):3541-3547.
[48] LIN J,LIN KJ,WANG YF,et al.Association of surgical margins with local recurrence in patients undergoing breast-conserving surgery after neoadjuvant chemotherapy[J].BMC Cancer,2020,20(1):451.