Skip to main content
Top
Published in: Breast Cancer Research and Treatment 2/2019

Open Access 01-11-2019 | Breast Cancer | Clinical trial

Pathologic complete response and outcomes by intrinsic subtypes in NSABP B-41, a randomized neoadjuvant trial of chemotherapy with trastuzumab, lapatinib, or the combination

Authors: Sandra M. Swain, Gong Tang, Peter C. Lucas, André Robidoux, David Goerlitz, Brent T. Harris, Hanna Bandos, Charles E. Geyer Jr., Priya Rastogi, Eleftherios P. Mamounas, Norman Wolmark

Published in: Breast Cancer Research and Treatment | Issue 2/2019

Login to get access

Abstract

Purpose

NSABP B-41, a phase three randomized trial, evaluated neoadjuvant lapatinib, trastuzumab, or the combination with chemotherapy in patients with HER2-positive operable breast cancer. Though no significant difference in pathologic complete response (pCR) was found among the three arms, pCR was associated with prolonged survival. We analyzed tumor intrinsic subtypes with Prediction Analysis of Microarray 50 in a subset of B-41 patients to determine their value in predicting HER2-targeting benefit.

Methods

Pearson’s Chi square test and logistic regression were used to compare pCR in the breast and nodes (ypT0/Tis ypN0). Kaplan–Meier estimates and Cox models were used to compare event-free and overall survival among subtypes.

Results

Intrinsic subtypes were determined in 271 baseline core biopsy samples. The pCR rate among patients with HER2-enriched (HER2E) subtype was greater compared to other subtypes combined (120/197, 60.9% versus 19/74, 25.7%; p < 0.001). In multivariate analysis among patients receiving trastuzumab-containing regimens (with clinical factors and HER2E subtype as factors), HER2E subtype was most strongly associated with pCR [OR 8.41 (95% CI 2.52–28.1) p < 0.001]. Patients with HER2E tumors did not benefit more from dual HER2-targeted therapy versus trastuzumab. The pCR rate was higher among HER2E tumors versus other subtypes in both estrogen receptor-positive and -negative tumors (p ≤ 0.001). Higher ESR1 gene expression was associated with lower pCR rate. No association was observed between subtype and long-term outcomes.

Conclusion

Patients with HER2E tumors were most likely to attain pCR versus other subtypes. HER2E subtype represents a favorable marker for predicting HER2-targeting benefit, particularly with trastuzumab-based therapies.
Appendix
Available only for authorised users
Literature
1.
2.
go back to reference Cameron D, Piccart-Gebhart MJ, Gelber RD et al (2017) 11 years’ follow-up of trastuzumab after adjuvant chemotherapy in HER2-positive early breast cancer: final analysis of the HERceptin Adjuvant (HERA) trial. Lancet 389:1195–1205CrossRefPubMedPubMedCentral Cameron D, Piccart-Gebhart MJ, Gelber RD et al (2017) 11 years’ follow-up of trastuzumab after adjuvant chemotherapy in HER2-positive early breast cancer: final analysis of the HERceptin Adjuvant (HERA) trial. Lancet 389:1195–1205CrossRefPubMedPubMedCentral
3.
go back to reference Cortazar P, Zhang L, Untch M et al (2014) Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis. Lancet 384:164–172CrossRefPubMed Cortazar P, Zhang L, Untch M et al (2014) Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis. Lancet 384:164–172CrossRefPubMed
4.
go back to reference Baselga J, Bradbury I, Eidtmann H et al (2012) Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial. Lancet 379:633–640CrossRefPubMedPubMedCentral Baselga J, Bradbury I, Eidtmann H et al (2012) Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial. Lancet 379:633–640CrossRefPubMedPubMedCentral
5.
go back to reference Robidoux A, Tang G, Rastogi P et al (2013) Lapatinib as a component of neoadjuvant therapy for HER2-positive operable breast cancer (NSABP protocol B-41): an open-label, randomised phase 3 trial. Lancet Oncol 14:1183–1192CrossRefPubMed Robidoux A, Tang G, Rastogi P et al (2013) Lapatinib as a component of neoadjuvant therapy for HER2-positive operable breast cancer (NSABP protocol B-41): an open-label, randomised phase 3 trial. Lancet Oncol 14:1183–1192CrossRefPubMed
6.
go back to reference Carey LA, Berry DA, Cirrincione CT et al (2016) Molecular heterogeneity and response to neoadjuvant human epidermal growth factor receptor 2 targeting in CALGB 40601, a randomized phase III trial of paclitaxel plus trastuzumab with or without lapatinib. J Clin Oncol 34:542–549CrossRefPubMed Carey LA, Berry DA, Cirrincione CT et al (2016) Molecular heterogeneity and response to neoadjuvant human epidermal growth factor receptor 2 targeting in CALGB 40601, a randomized phase III trial of paclitaxel plus trastuzumab with or without lapatinib. J Clin Oncol 34:542–549CrossRefPubMed
7.
go back to reference Hicks M, Macrae ER, Abdel-Rasoul M et al (2015) Neoadjuvant dual HER2-targeted therapy with lapatinib and trastuzumab improves pathologic complete response in patients with early stage HER2-positive breast cancer: a meta-analysis of randomized prospective clinical trials. Oncologist 20:337–343CrossRefPubMedPubMedCentral Hicks M, Macrae ER, Abdel-Rasoul M et al (2015) Neoadjuvant dual HER2-targeted therapy with lapatinib and trastuzumab improves pathologic complete response in patients with early stage HER2-positive breast cancer: a meta-analysis of randomized prospective clinical trials. Oncologist 20:337–343CrossRefPubMedPubMedCentral
8.
go back to reference Clavarezza M, Puntoni M, Gennari A et al (2016) Dual block with lapatinib and trastuzumab versus single-agent trastuzumab combined with chemotherapy as neoadjuvant treatment of HER2-positive breast cancer: a meta-analysis of randomized trials. Clin Cancer Res 22:4594–4603CrossRefPubMed Clavarezza M, Puntoni M, Gennari A et al (2016) Dual block with lapatinib and trastuzumab versus single-agent trastuzumab combined with chemotherapy as neoadjuvant treatment of HER2-positive breast cancer: a meta-analysis of randomized trials. Clin Cancer Res 22:4594–4603CrossRefPubMed
9.
go back to reference Robidoux A, Tang G, Rastogi P et al (2016) Evaluation of lapatinib as a component of neoadjuvant therapy for HER2 + operable breast cancer: five year outcomes of NSABP protocol B-41. J Clin Oncol 34:501CrossRef Robidoux A, Tang G, Rastogi P et al (2016) Evaluation of lapatinib as a component of neoadjuvant therapy for HER2 + operable breast cancer: five year outcomes of NSABP protocol B-41. J Clin Oncol 34:501CrossRef
10.
11.
go back to reference Dieci MV, Prat A, Tagliafico E et al (2016) Integrated evaluation of PAM50 subtypes and immune modulation of pCR in HER2-positive breast cancer patients treated with chemotherapy and HER2-targeted agents in the CherLOB trial. Ann Oncol 27:1867–1873CrossRefPubMed Dieci MV, Prat A, Tagliafico E et al (2016) Integrated evaluation of PAM50 subtypes and immune modulation of pCR in HER2-positive breast cancer patients treated with chemotherapy and HER2-targeted agents in the CherLOB trial. Ann Oncol 27:1867–1873CrossRefPubMed
12.
go back to reference Prat A, Bianchini G, Thomas M et al (2014) Research-based PAM50 subtype predictor identifies higher responses and improved survival outcomes in HER2-positive breast cancer in the NOAH study. Clin Cancer Res 20:511–521CrossRefPubMed Prat A, Bianchini G, Thomas M et al (2014) Research-based PAM50 subtype predictor identifies higher responses and improved survival outcomes in HER2-positive breast cancer in the NOAH study. Clin Cancer Res 20:511–521CrossRefPubMed
13.
go back to reference Fumagalli D, Venet D, Ignatiadis M et al (2017) RNA sequencing to predict response to neoadjuvant anti-HER2 therapy: a secondary analysis of the NeoALTTO randomized clinical trial. JAMA Oncol 3:227–234CrossRefPubMedPubMedCentral Fumagalli D, Venet D, Ignatiadis M et al (2017) RNA sequencing to predict response to neoadjuvant anti-HER2 therapy: a secondary analysis of the NeoALTTO randomized clinical trial. JAMA Oncol 3:227–234CrossRefPubMedPubMedCentral
14.
go back to reference McShane LM, Altman DG, Sauerbrei W et al (2005) Reporting recommendations for tumor marker prognostic studies (REMARK). J Natl Cancer Inst 97:1180–1184CrossRefPubMed McShane LM, Altman DG, Sauerbrei W et al (2005) Reporting recommendations for tumor marker prognostic studies (REMARK). J Natl Cancer Inst 97:1180–1184CrossRefPubMed
15.
go back to reference Jørgensen CL, Nielsen TO, Bjerre KD et al (2014) PAM50 breast cancer intrinsic subtypes and effect of gemcitabine in advanced breast cancer patients. Acta Oncol 53:776–787CrossRefPubMed Jørgensen CL, Nielsen TO, Bjerre KD et al (2014) PAM50 breast cancer intrinsic subtypes and effect of gemcitabine in advanced breast cancer patients. Acta Oncol 53:776–787CrossRefPubMed
16.
go back to reference Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B Stat Methodol 57:289–300 Benjamini Y, Hochberg Y (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Series B Stat Methodol 57:289–300
17.
go back to reference Hommel G (1988) A stagewise rejective multiple test procedure based on a modified Bonferroni test. Biometrika 75:383–386CrossRef Hommel G (1988) A stagewise rejective multiple test procedure based on a modified Bonferroni test. Biometrika 75:383–386CrossRef
18.
go back to reference Akaike H (1974) A new look at the statistical model identification. IEEE Trans Automat Contr 19:716–723CrossRef Akaike H (1974) A new look at the statistical model identification. IEEE Trans Automat Contr 19:716–723CrossRef
19.
go back to reference Gianni L, Pienkowski T, Im Y-H et al (2012) 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. Lancet Oncol 13:25–32CrossRefPubMed Gianni L, Pienkowski T, Im Y-H et al (2012) 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. Lancet Oncol 13:25–32CrossRefPubMed
20.
go back to reference Cejalvo JM, Pascuala T, Fernández-Martíneze A et al (2018) Clinical implications of the non-luminal intrinsic subtypes in hormone receptor-positive breast cancer. Cancer Treat Rev 67:63–70CrossRefPubMed Cejalvo JM, Pascuala T, Fernández-Martíneze A et al (2018) Clinical implications of the non-luminal intrinsic subtypes in hormone receptor-positive breast cancer. Cancer Treat Rev 67:63–70CrossRefPubMed
21.
go back to reference Llombart-Cussac A, Cortés J, Paré L et al (2017) HER2-enriched subtype as a predictor of pathological complete response following trastuzumab and lapatinib without chemotherapy in early-stage HER2-positive breast cancer (PAMELA): an open-label, single-group, multicentre, phase 2 trial. Lancet Oncol 18:545–554CrossRefPubMed Llombart-Cussac A, Cortés J, Paré L et al (2017) HER2-enriched subtype as a predictor of pathological complete response following trastuzumab and lapatinib without chemotherapy in early-stage HER2-positive breast cancer (PAMELA): an open-label, single-group, multicentre, phase 2 trial. Lancet Oncol 18:545–554CrossRefPubMed
22.
go back to reference Buzdar AU, Ibrahim NK, Francis D et al (2005) Buzdar 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 23:3676–3685CrossRefPubMed Buzdar AU, Ibrahim NK, Francis D et al (2005) Buzdar 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 23:3676–3685CrossRefPubMed
24.
go back to reference Guarneri V, Frassoldati A, Bottini A et al (2012) Preoperative chemotherapy plus trastuzumab, lapatinib, or both in human epidermal growth factor receptor 2–positive operable breast cancer: results of the randomized phase II CHER-LOB study. J Clin Oncol 30:1989–1995CrossRefPubMed Guarneri V, Frassoldati A, Bottini A et al (2012) Preoperative chemotherapy plus trastuzumab, lapatinib, or both in human epidermal growth factor receptor 2–positive operable breast cancer: results of the randomized phase II CHER-LOB study. J Clin Oncol 30:1989–1995CrossRefPubMed
25.
go back to reference Prat A, Cheang MCU, Galvan P et al (2016) Prognostic value of intrinsic subtypes in hormone receptor– positive metastatic breast cancer treated with letrozole with or without lapatinib. JAMA Oncol 2:1287–1294CrossRefPubMed Prat A, Cheang MCU, Galvan P et al (2016) Prognostic value of intrinsic subtypes in hormone receptor– positive metastatic breast cancer treated with letrozole with or without lapatinib. JAMA Oncol 2:1287–1294CrossRefPubMed
26.
go back to reference Fernandez-Martinez A, Tanioka M, Fan C et al (2019) Genomic-based predictive biomarkers to anti-HER2 therapies: a combined analysis of CALGB 40601 (Alliance) and PAMELA clinical trials. J Clin Oncol 37:571CrossRef Fernandez-Martinez A, Tanioka M, Fan C et al (2019) Genomic-based predictive biomarkers to anti-HER2 therapies: a combined analysis of CALGB 40601 (Alliance) and PAMELA clinical trials. J Clin Oncol 37:571CrossRef
27.
go back to reference Swain SM, Ewer MS, Viale G et al (2018) Pertuzumab, trastuzumab, and standard anthracycline- and taxane-based chemotherapy for the neoadjuvant treatment of patients with HER2-positive localized breast cancer (BERENICE): a phase II, open-label, multicentre, multinational cardiac safety study. Ann Oncol 29:646–653CrossRefPubMed Swain SM, Ewer MS, Viale G et al (2018) Pertuzumab, trastuzumab, and standard anthracycline- and taxane-based chemotherapy for the neoadjuvant treatment of patients with HER2-positive localized breast cancer (BERENICE): a phase II, open-label, multicentre, multinational cardiac safety study. Ann Oncol 29:646–653CrossRefPubMed
Metadata
Title
Pathologic complete response and outcomes by intrinsic subtypes in NSABP B-41, a randomized neoadjuvant trial of chemotherapy with trastuzumab, lapatinib, or the combination
Authors
Sandra M. Swain
Gong Tang
Peter C. Lucas
André Robidoux
David Goerlitz
Brent T. Harris
Hanna Bandos
Charles E. Geyer Jr.
Priya Rastogi
Eleftherios P. Mamounas
Norman Wolmark
Publication date
01-11-2019
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 2/2019
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-019-05398-3

Other articles of this Issue 2/2019

Breast Cancer Research and Treatment 2/2019 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine