Abstract
Keywords
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Clinical Breast CancerReferences
- Surgical issues in patients with breast cancer receiving neoadjuvant chemotherapy.Nat Rev Clin Oncol. 2015; 12: 335-343
- Neoadjuvant therapy for early-stage breast cancer: current practice, controversies, and future directions.Oncology (Williston Park). 2015; 29: 828-838
- Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes.J Clin Oncol. 2012; 30: 1796-1804
- Neoadjuvant versus adjuvant systemic treatment in breast cancer: a meta-analysis.J Natl Cancer Inst. 2005; 97: 188-194
- Predictors of locoregional recurrence after neoadjuvant chemotherapy: results from combined analysis of National Surgical Adjuvant Breast and Bowel Project B-18 and B-27.J Clin Oncol. 2012; 30: 3960-3966
- Predictors of locoregional recurrence after failure to achieve pathologic complete response to neoadjuvant chemotherapy in triple-negative breast cancer.J Natl Compr Canc Netw. 2019; 17: 348-356
- Pathologic response after neoadjuvant chemotherapy predicts locoregional control in patients with triple negative breast cancer.Adv Radiat Oncol. 2017; 2: 105-109
- Residual cancer burden after neoadjuvant therapy and long-term survival outcomes in breast cancer: a multi-center pooled analysis.2019 (Paper presented at: San Antonio Breast Cancer Symposium, 2019; San Antonio, Texas, December 10-14)
- Neoadjuvant therapy for early-stage breast cancer: a model for individualizing outcomes and tailoring locoregional and systemic therapy.Oncology (Williston Park). 2015; 29 (846): 839-840
- Room for improvement in breast cancer clinical trial design: taking advantage of the preoperative setting.J Comp Eff Res. 2013; 2: 393-403
- Trial-level prediction of long-term outcome based on pathologic complete response (pCR) after neoadjuvant chemotherapy for early-stage breast cancer (EBC).Contemp Clin Trials. 2018; 71: 194-198
- Meta-analysis on the association between pathologic complete response and triple-negative breast cancer after neoadjuvant chemotherapy.World J Surg Oncol. 2014; 12: 95
- Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis.Lancet. 2014; 384: 164-172
United States Food and Drug Administration. Pathologic complete response in neoadjuvant treatment of high-risk early-stage breast cancer: use as an endpoint to support accelerated approval; guidance for industry; availability. Available at: https://www.fda.gov/regulatory-information/search-fda-guidance-documents/pathologic-complete-response-neoadjuvant-treatment-high-risk-early-stage-breast-cancer-use-endpoint. In. Vol 79. Fed Regist2014:60476-60477. Accessed July 27, 2020.
- Comparison of different definitions of pathologic complete response in operable breast cancer: a pooled analysis of three prospective neoadjuvant studies of JBCRG.Breast Cancer. 2015; 22: 586-595
- Significantly higher pathologic complete remission rate after neoadjuvant therapy with trastuzumab, paclitaxel, and epirubicin chemotherapy: results of a randomized trial in human epidermal growth factor receptor 2-positive operable breast cancer.J Clin Oncol. 2005; 23: 3676-3685
- Sequential preoperative or postoperative docetaxel added to preoperative doxorubicin plus cyclophosphamide for operable breast cancer:National Surgical Adjuvant Breast and Bowel Project Protocol B-27.J Clin Oncol. 2006; 24: 2019-2027
- Statistical controversies in clinical research: assessing pathologic complete response as a trial-level surrogate end point for early-stage breast cancer.Ann Oncol. 2016; 27: 10-15
- Prognostic significance of subtype and pathologic response in operable breast cancer; a pooled analysis of prospective neoadjuvant studies of JBCRG.Breast Cancer. 2015; 22: 486-495
- Pathologic complete response as a potential surrogate for the clinical outcome in patients with breast cancer after neoadjuvant therapy: a meta-regression of 29 randomized prospective studies.J Clin Oncol. 2014; 32: 3883-3891
- Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial.Lancet. 2012; 379: 633-640
- Updated results from the phase III ALTTO trial (BIG 2-06; NCCTG (Alliance) N063D) comparing one year of anti-HER2 therapy with lapatinib alone (L), trastuzumab alone (T), their sequence (T → L) or their combination (L + T) in the adjuvant treatment of HER2-positive early breast cancer.J Clin Oncol. 2017; 35: 502
- Neoadjuvant chemotherapy for operable breast cancer.Br J Surg. 2007; 94: 1189-1200
- Pathological complete response (pCR) after neoadjuvant chemotherapy and impact on breast cancer recurrence and survival, stratified by breast cancer subtypes and adjuvant chemotherapy usage: patient-level meta-analyses of over 27,000 patients. Proceedings from the 2018 San Antonio Breast Cancer Symposium (SABCS); December 4-8.2018 (San Antonio, TX)
- Adaptive randomization of veliparib-carboplatin treatment in breast cancer.N Engl J Med. 2016; 375: 23-34
- Pathological complete response predicts event-free and distant disease-free survival in the I-SPY2 TRIAL.Cancer Res. 2018; 78: GS3-GS08
- Adjuvant capecitabine for breast cancer after preoperative chemotherapy.N Engl J Med. 2017; 376: 2147-2159
- The use of neoadjuvant platinum-based chemotherapy in locally advanced breast cancer that is triple negative: retrospective analysis of 144 patients.Breast Cancer Res Treat. 2013; 138: 783-794
- Neoadjuvant chemotherapy for breast cancer: functional tumor volume by MR imaging predicts recurrence-free survival-results from the ACRIN 6657/CALGB 150007 I-SPY 1 TRIAL.Radiology. 2016; 279: 44-55
- Breast cancer subtype influences the accuracy of predicting pathologic response by imaging and clinical breast exam after neoadjuvant chemotherapy.Anticancer Res. 2016; 36: 5389-5395
- TBCRC 008: early change in 18F-FDG uptake on PET predicts response to preoperative systemic therapy in human epidermal growth factor receptor 2-negative primary operable breast cancer.J Nucl Med. 2015; 56: 31-37
- Evaluation of contrast-enhanced ultrasonography for early prediction of response to neoadjuvant chemotherapy in triple negative breast cancer.Cancer Research. 2017; 77 (abstract P4-02-06)
- Prognostic value of tumor-infiltrating lymphocytes on residual disease after primary chemotherapy for triple-negative breast cancer: a retrospective multicenter study.Ann Oncol. 2015; 26: 1518
- Tumor-infiltrating lymphocytes and response to neoadjuvant chemotherapy with or without carboplatin in human epidermal growth factor receptor 2-positive and triple-negative primary breast cancers.J Clin Oncol. 2015; 33: 983-991
- The value of tumor infiltrating lymphocytes (TILs) for predicting response to neoadjuvant chemotherapy in breast cancer: a systematic review and meta-analysis.PLoS One. 2014; 9: e115103
- The prognostic value of tumor-infiltrating lymphocytes in triple-negative breast cancer: a meta-analysis.Breast Cancer Res Treat. 2014; 148: 467-476
- Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.J Clin Oncol. 2015; 33: 304-311
- Abnormalities of the inactive X chromosome are a common feature of BRCA1 mutant and sporadic basal-like breast cancer.Cold Spring Harb Symp Quant Biol. 2005; 70: 93-97
- Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancers.Cancer Res. 2004; 64: 64-71
- X chromosomal abnormalities in basal-like human breast cancer.Cancer Cell. 2006; 9: 121-132
- Hallmarks of ‘BRCAness’ in sporadic cancers.Nat Rev Cancer. 2004; 4: 814-819
- BRCAness revisited.Nat Rev Cancer. 2016; 16: 110-120
- Germline mutations in DNA repair genes may predict neoadjuvant therapy response in triple negative breast patients.Genes Chromosomes Cancer. 2016; 55: 915-924
- BRCAness and prognosis in triple-negative breast cancer patients treated with neoadjuvant chemotherapy.PLoS One. 2016; 11: e0165721
- TBCRC 030: a randomized phase II study of preoperative cisplatin versus paclitaxel in TNBC—evaluating the homologous recombination deficiency (HRD) biomarker.J Clin Oncol. 2019; 37: 507
- Comparison of 12 weeks neoadjuvant nab-paclitaxel combined with carboplatinum vs. gemcitabine in triple negative breast cancer: WSG-ADAPT TN randomized phase II trial. Paper presented at: Oncology Research and Treatment, 2016; August 4-6.2016 (Toronto, Ontario, Canada)
- Efficacy of neoadjuvant carboplatin plus docetaxel in triple-negative breast cancer: combined analysis of two cohorts.Clin Cancer Res. 2017; 23: 649-657
- Pathological response and survival in triple-negative breast cancer following neoadjuvant carboplatin plus docetaxel.Clin Cancer Res. 2018; 24: 5820-5829
- Comparison of residual cancer burden, American Joint Committee on Cancer staging and pathologic complete response in breast cancer after neoadjuvant chemotherapy: results from the I-SPY 1 TRIAL (CALGB 150007/150012; ACRIN 6657).Breast Cancer Res Treat. 2017; 165: 181-191
- Neoadjuvant carboplatin in patients with triple-negative and HER2-positive early breast cancer (GeparSixto; GBG 66): a randomised phase 2 trial.Lancet Oncol. 2014; 15: 747-756
- Neoadjuvant chemotherapy considerations in triple-negative breast cancer.J Target Ther Cancer. 2018; 7: 52-69
- Efficacy of carboplatin-based preoperative chemotherapy for triple-negative breast cancer. A meta-analysis of randomized controlled trials.Saudi Med J. 2017; 38: 18-23
- Impact of the addition of carboplatin and/or bevacizumab to neoadjuvant once-per-week paclitaxel followed by dose-dense doxorubicin and cyclophosphamide on pathologic complete response rates in stage II to III triple-negative breast cancer: CALGB 40603 (Alliance).J Clin Oncol. 2015; 33: 13-21
- Final efficacy and updated safety results of the randomized phase III BEATRICE trial evaluating adjuvant bevacizumab-containing therapy in triple-negative early breast cancer.Ann Oncol. 2017; 28: 754-760
- Neoadjuvant bevacizumab and anthracycline-taxane-based chemotherapy in 678 triple-negative primary breast cancers; results from the geparquinto study (GBG 44).Ann Oncol. 2013; 24: 2978-2984
- Bevacizumab in the neoadjuvant treatment of human epidermal growth factor receptor 2-negative breast cancer: a meta-analysis of randomized controlled trials.Mol Clin Oncol. 2019; 10: 357-365
- Bevacizumab in the treatment of metastatic breast cancer: friend or foe?.Curr Oncol Rep. 2012; 14: 1-11
- NeoTRIPaPDL1 Michelangelo randomized study. Pathologic complete response (pCR) to neoadjuvant treatment with or without atezolizumab in triple negative, early high-risk and locally advanced breast cancer.Cancer Res. 2020; 80 (GS3-04)
- GS3-03. KEYNOTE-522 study of neoadjuvant pembrolizumab + chemotherapy vs placebo + chemotherapy, followed by adjuvant pembrolizumab vs placebo for early triple-negative breast cancer: pathologic complete response in key subgroups and by treatment exposure, residual cancer burden, and breast-conserving surgery.2019 (Presented at San Antonio Breast Cancer Symposium; San Antonio, TX: December 10-14)
- Talazoparib in Patients with Advanced Breast Cancer and a Germline BRCA Mutation.N Engl J Med. 2018; 379: 753-763
- Addition of the PARP inhibitor veliparib plus carboplatin or carboplatin alone to standard neoadjuvant chemotherapy in triple-negative breast cancer (BrighTNess): a randomised, phase 3 trial.Lancet Oncol. 2018; 19: 497-509
- Abstract OT2-01-15: PARTNER-Randomised, phase II/III trial to evaluate the safety and efficacy of the addition of olaparib to platinum-based neoadjuvant chemotherapy in triple negative and/or germline BRCA mutated breast cancer patients.2016 (Presented at San Antonio Breast Cancer Symposium; San Antonio, TX: December 6-10)
- GeparOLA: A randomized phase II trial to assess the efficacy of paclitaxel and olaparib in comparison to paclitaxel/carboplatin followed by epirubicin/cyclophosphamide as neoadjuvant chemotherapy in patients (pts) with HER2-negative early breast cancer (BC) and homologous recombination deficiency (HRD).J Clin Oncol. 2019; 37: 506
- Significantly longer progression-free survival with nab-paclitaxel compared with docetaxel as first-line therapy for metastatic breast cancer.J Clin Oncol. 2009; 27: 3611-3619
- German Breast Group (GBG); Arbeitsgemeinschaft Gynäkologische Onkologie—Breast (AGO-B) Investigators. Nab-paclitaxel versus solvent-based paclitaxel in neoadjuvant chemotherapy for early breast cancer (GeparSepto-GBG 69): a randomised, phase 3 trial.Lancet Oncol. 2016; 17: 345-356
- I-SPY 2: an adaptive breast cancer trial design in the setting of neoadjuvant chemotherapy.Clin Pharmacol Ther. 2009; 86: 97-100
- Phase III randomized, placebo-controlled trial of carboplatin (C) and paclitaxel (P) with/without veliparib (ABT-888) in HER2-BRCA-associated locally advanced or metastatic breast cancer (BC).J Clin Oncol. 2015; 33: 155
- Pembrolizumab plus standard neoadjuvant therapy for high-risk breast cancer (BC): results from I-SPY 2.J Clin Oncol. 2017; 35: 506