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Published in: Breast Cancer Research and Treatment 3/2020

01-04-2020 | Metastasis | Epidemiology

Management of the axilla in breast cancer: outcome analysis in a series of ductal versus lobular invasive cancers

Authors: S. P. Corona, M. Bortul, S. Scomersi, C. Bigal, C. Bottin, F. Zanconati, S. B. Fox, F. Giudici, D. Generali

Published in: Breast Cancer Research and Treatment | Issue 3/2020

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Abstract

Introduction

Axillary lymph node dissection (ALND) has been considered essential for the staging of breast cancer (BC). As the impact of tumor biology on clinical outcomes is recognized, a surgical de-escalation approach is being implemented. We performed a retrospective study focused on surgical management of the axilla in invasive lobular carcinoma (ILC) versus invasive ductal carcinoma (IDC).

Materials and methods

1151 newly diagnosed BCs, IDCs (79.6%) or ILCs (20.4%), were selected among patients treated at our Breast Cancer Unit from 2012 to 2018. Tumor characteristics and clinical information were collected and predictors of further metastasis after positive sentinel lymph node biopsy (SLNB) analyzed in relation to disease-free survival (DFS) and overall survival (OS).

Results

27.5% of patients with ILC had ≥ 3 metastatic lymph nodes at ALND after positive SLNB versus 11.48% of IDCs (p = 0.04). Risk predictors of further metastasis at ALND were the presence of > 2 positive lymph nodes at SLNB (OR = 4.72, 95% CI 1.15–19.5 p = 0.03), T3–T4 tumors (OR = 4.93, 95% CI 1.10–22.2, p = 0.03) and Non-Luminal BC (OR = 2.74, 95% CI 1.16–6.50, p = 0.02). The lobular histotype was not associated with the risk of further metastasis at ALND (OR = 1.62, 95% CI 0.77–3.41, p = 0.20).

Conclusions

ILC histology is not associated with higher risk of further metastasis at ALND in our analysis. However, surgical management decisions should be taken considering tumor histotype, biology and expected sensitivity to adjuvant therapies.
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Literature
1.
go back to reference Lowery AJ, Kell MR, Glynn RW et al (2012) Locoregional recurrence after breast cancer surgery: a systematic review by receptor phenotype. Breast Cancer Res Treat 133(3):831–841CrossRef Lowery AJ, Kell MR, Glynn RW et al (2012) Locoregional recurrence after breast cancer surgery: a systematic review by receptor phenotype. Breast Cancer Res Treat 133(3):831–841CrossRef
2.
go back to reference Lucci A, Mc Call LM, Beitsch PD et al (2007) American College of Surgeons Oncology Group: surgical complication associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group Trial Z0011. J Clin Oncol 25(24):3657–3663CrossRef Lucci A, Mc Call LM, Beitsch PD et al (2007) American College of Surgeons Oncology Group: surgical complication associated with sentinel lymph node dissection (SLND) plus axillary lymph node dissection compared with SLND alone in the American College of Surgeons Oncology Group Trial Z0011. J Clin Oncol 25(24):3657–3663CrossRef
4.
go back to reference Giuliano AE, Ballman KV, McCall L et al (2017) 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. JAMA 318:918–925CrossRef Giuliano AE, Ballman KV, McCall L et al (2017) 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. JAMA 318:918–925CrossRef
5.
go back to reference Fisher B, Anderson S, Bryant J et al (2002) Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med 347:1233–1241CrossRef Fisher B, Anderson S, Bryant J et al (2002) Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. N Engl J Med 347:1233–1241CrossRef
6.
go back to reference Mansel RE, Fallowfield L, Kissin M et al (2006) Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J NatlCancerInst 98:599–609 Mansel RE, Fallowfield L, Kissin M et al (2006) Randomized multicenter trial of sentinel node biopsy versus standard axillary treatment in operable breast cancer: the ALMANAC Trial. J NatlCancerInst 98:599–609
7.
go back to reference Veronesi U, Viale G, Paganelli G et al (2010) Sentinel lymph node biopsy in breast cancer: ten-year results of a randomized controlled study. Ann Surg 251:595–600CrossRef Veronesi U, Viale G, Paganelli G et al (2010) Sentinel lymph node biopsy in breast cancer: ten-year results of a randomized controlled study. Ann Surg 251:595–600CrossRef
8.
go back to reference Krag DN, Anderson SJ, Julian TB et al (2010) Sentinel lymph-node resection compared with conventional axillary lymph-node dissection in clinically node-negative patients with breast cancer: overall survival findings from the NSABP B-32 randomized phase 3 trial. Lancet Oncol 11:927–933CrossRef Krag DN, Anderson SJ, Julian TB et al (2010) Sentinel lymph-node resection compared with conventional axillary lymph-node dissection in clinically node-negative patients with breast cancer: overall survival findings from the NSABP B-32 randomized phase 3 trial. Lancet Oncol 11:927–933CrossRef
9.
go back to reference Giuliano AE, Hunt KK, Ballman KV et al (2011) Axillary dissection vs no axillary dissection in women with invasive breast cancer and sentinel node metastasis: a randomized clinical trial. JAMA 305:569–575CrossRef Giuliano AE, Hunt KK, Ballman KV et al (2011) Axillary dissection vs no axillary dissection in women with invasive breast cancer and sentinel node metastasis: a randomized clinical trial. JAMA 305:569–575CrossRef
11.
14.
go back to reference Bevilacqua JL, Kattan MW, Fey JV et al (2007) Doctor, what are my chances of having a positive sentinel node? A validated nomogram for risk estimation. J Clin Oncol 25:3670–3679CrossRef Bevilacqua JL, Kattan MW, Fey JV et al (2007) Doctor, what are my chances of having a positive sentinel node? A validated nomogram for risk estimation. J Clin Oncol 25:3670–3679CrossRef
15.
go back to reference Chen JY, Chen JJ, Yang BL, et al. Predicting sentinel lymph node metastasis in a Chinese breast cancer population: assessment of an existing nomogram and a new predictive nomogram. Breast Canc Res Treat 2012;135:839e48CrossRef Chen JY, Chen JJ, Yang BL, et al. Predicting sentinel lymph node metastasis in a Chinese breast cancer population: assessment of an existing nomogram and a new predictive nomogram. Breast Canc Res Treat 2012;135:839e48CrossRef
16.
go back to reference Yeniay L, Carti E, Karaca C et al (2012) A new and simple predictive formula for nonsentinel lymph node metastasis in breast cancer patients with positive sentinel lymph nodes, and validation of 3 different nomograms in Turkish breast cancer patients. Breast Care 7:397–402CrossRef Yeniay L, Carti E, Karaca C et al (2012) A new and simple predictive formula for nonsentinel lymph node metastasis in breast cancer patients with positive sentinel lymph nodes, and validation of 3 different nomograms in Turkish breast cancer patients. Breast Care 7:397–402CrossRef
17.
go back to reference Coombs N, Chen W, Taylor R, Boyages J (2007) A decision tool for predicting sentinel node accuracy from breast tumor size and grade. Breast J 13:593–598CrossRef Coombs N, Chen W, Taylor R, Boyages J (2007) A decision tool for predicting sentinel node accuracy from breast tumor size and grade. Breast J 13:593–598CrossRef
19.
go back to reference Fernandez B, Paish EC, Green AR et al. Lymph-node metastases in invasive lobular carcinoma are different from those in ductal carcinoma of the breast. J Clin Pathol 2011;64:995–1000CrossRefPubMed Fernandez B, Paish EC, Green AR et al. Lymph-node metastases in invasive lobular carcinoma are different from those in ductal carcinoma of the breast. J Clin Pathol 2011;64:995–1000CrossRefPubMed
22.
go back to reference Gebhardt BJ, Thomas J, Horne ZD et al. Is completion axillary lymph node dissection necessary in patients who are underrepresented in the ACOSOG Z0011 trial? Adv Radiat Oncol 2018:3(3): 258–264.doi: 10.1016/j.adro.2018.03.004.CrossRefPubMedPubMedCentral Gebhardt BJ, Thomas J, Horne ZD et al. Is completion axillary lymph node dissection necessary in patients who are underrepresented in the ACOSOG Z0011 trial? Adv Radiat Oncol 2018:3(3): 258–264.doi: 10.1016/j.adro.2018.03.004.CrossRefPubMedPubMedCentral
24.
go back to reference Donker M, van Tienhoven G, Straver ME et al (2014) Radiotherapy or surgery of the axilla after a positive sentinel node in breast cancer (EORTC 10981–22023 AMAROS): a randomised, multicentre, open-label, phase 3 non-inferiority trial. Lancet Oncol 15:1303–1310CrossRef Donker M, van Tienhoven G, Straver ME et al (2014) Radiotherapy or surgery of the axilla after a positive sentinel node in breast cancer (EORTC 10981–22023 AMAROS): a randomised, multicentre, open-label, phase 3 non-inferiority trial. Lancet Oncol 15:1303–1310CrossRef
25.
go back to reference Adachi Y, Ishiguro J, Kotani H et al (2016) Comparison of clinical outcomes between luminal invasive ductal carcinoma and luminal invasive lobular carcinoma. BMC Cancer 16:248CrossRef Adachi Y, Ishiguro J, Kotani H et al (2016) Comparison of clinical outcomes between luminal invasive ductal carcinoma and luminal invasive lobular carcinoma. BMC Cancer 16:248CrossRef
26.
go back to reference Van Wyhe RD, Claudle AS, Shaitelman SF et al (2018) A component of lobular carcinoma in clinically lymph node–negative patients predicts for an increased likelihood of upstaging to pathologic stage III breast cancer. Advances in Radiation Oncology 3:252–257CrossRef Van Wyhe RD, Claudle AS, Shaitelman SF et al (2018) A component of lobular carcinoma in clinically lymph node–negative patients predicts for an increased likelihood of upstaging to pathologic stage III breast cancer. Advances in Radiation Oncology 3:252–257CrossRef
27.
go back to reference Arpino G, Bardou VJ, Clark GM et al (2004) Infiltrating lobular carcinoma of the breast: tumor characteristics and clinical outcome. Breast Cancer Res 6:R149–R156CrossRef Arpino G, Bardou VJ, Clark GM et al (2004) Infiltrating lobular carcinoma of the breast: tumor characteristics and clinical outcome. Breast Cancer Res 6:R149–R156CrossRef
28.
go back to reference Li CI, Uribe DJ, Daling JR (2005) Clinical characteristics of different histologic types of breast cancer. Br J Cancer 93:1046–1052CrossRef Li CI, Uribe DJ, Daling JR (2005) Clinical characteristics of different histologic types of breast cancer. Br J Cancer 93:1046–1052CrossRef
29.
go back to reference Weinberg ES, Dickson D, White L et al (2004) Cytokeratin staining for intraoperative evaluation of sentinel lymph nodes in patients with invasive lobular carcinoma. Am J Surg 188:419–422CrossRef Weinberg ES, Dickson D, White L et al (2004) Cytokeratin staining for intraoperative evaluation of sentinel lymph nodes in patients with invasive lobular carcinoma. Am J Surg 188:419–422CrossRef
30.
32.
go back to reference Tiernan JP, Verghese ET, Nair A et al (2014) Systematic review and meta-analysis of cytokeratin 19-based one-step nucleic acid amplification versus histopathology for sentinel lymph node assessment in breast cancer. Br J Surg 101:298–306 (PMID: 24536007) CrossRef Tiernan JP, Verghese ET, Nair A et al (2014) Systematic review and meta-analysis of cytokeratin 19-based one-step nucleic acid amplification versus histopathology for sentinel lymph node assessment in breast cancer. Br J Surg 101:298–306 (PMID: 24536007) CrossRef
33.
go back to reference Wasif N, Maggard MA, Ko CY et al. Invasive lobular vs. ductal breast cancer: a stage-matched comparison of outcomes. Ann Surg Oncol. 2010; 17: 1862–1869CrossRef Wasif N, Maggard MA, Ko CY et al. Invasive lobular vs. ductal breast cancer: a stage-matched comparison of outcomes. Ann Surg Oncol. 2010; 17: 1862–1869CrossRef
34.
go back to reference Hsiao YH, Tsai HD, Chou MC et al (2011) The myoepithelial cell layer may serve as a potential trigger factor for different outcomes of stage-matched invasive lobular and ductal breast cancers. Int J Biol Sci 7:147–153CrossRef Hsiao YH, Tsai HD, Chou MC et al (2011) The myoepithelial cell layer may serve as a potential trigger factor for different outcomes of stage-matched invasive lobular and ductal breast cancers. Int J Biol Sci 7:147–153CrossRef
36.
go back to reference Truin W, Voogd AC, Vreugdenhil G et al (2012) Effect of adjuvant chemotherapy in postmenopausal patients with invasive ductal versus lobular breast cancer. Ann Oncol 23:2859–2865CrossRef Truin W, Voogd AC, Vreugdenhil G et al (2012) Effect of adjuvant chemotherapy in postmenopausal patients with invasive ductal versus lobular breast cancer. Ann Oncol 23:2859–2865CrossRef
37.
go back to reference Davies C, Godwin J, Gray R et al (2011) Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: patient-level metaanalysis of randomised trials. Lancet 378:771–784CrossRef Davies C, Godwin J, Gray R et al (2011) Relevance of breast cancer hormone receptors and other factors to the efficacy of adjuvant tamoxifen: patient-level metaanalysis of randomised trials. Lancet 378:771–784CrossRef
38.
go back to reference MetzgerFilho O, Giobbie-Hurder A, Mallon E et al (2015) Relative effectiveness of letrozole compared with tamoxifen for patients with lobular carcinoma in the BIG 1–98 trial. J Clin Oncol 33:2772–2779CrossRef MetzgerFilho O, Giobbie-Hurder A, Mallon E et al (2015) Relative effectiveness of letrozole compared with tamoxifen for patients with lobular carcinoma in the BIG 1–98 trial. J Clin Oncol 33:2772–2779CrossRef
39.
go back to reference Rakha EA, Ellis IO (2010) Lobular breast carcinoma and its variants. Semin Diagn Pathol 27:49–61CrossRef Rakha EA, Ellis IO (2010) Lobular breast carcinoma and its variants. Semin Diagn Pathol 27:49–61CrossRef
40.
go back to reference Braunstein LZ, Brock JE, Chen YH et al (2015) Invasive lobular carcinoma of the breast: local recurrence after breast-conserving therapy by subtype approximation and surgical margin. Breast Cancer Res Treat 149:555–564CrossRef Braunstein LZ, Brock JE, Chen YH et al (2015) Invasive lobular carcinoma of the breast: local recurrence after breast-conserving therapy by subtype approximation and surgical margin. Breast Cancer Res Treat 149:555–564CrossRef
41.
go back to reference Sagara Y, Barry WT, Mallory MA et al (2015) Surgical options and locoregional recurrence in patients diagnosed with invasive lobular carcinoma of the breast. Ann Surg Oncol 22:4280–4286CrossRef Sagara Y, Barry WT, Mallory MA et al (2015) Surgical options and locoregional recurrence in patients diagnosed with invasive lobular carcinoma of the breast. Ann Surg Oncol 22:4280–4286CrossRef
42.
go back to reference Stecklein SR, Shen X, Mitchell MP (2016) Post-mastectomy radiation therapy for invasive lobular carcinoma: a comparative utilization and outcomes study. Clin Breast Cancer 16:319–326CrossRef Stecklein SR, Shen X, Mitchell MP (2016) Post-mastectomy radiation therapy for invasive lobular carcinoma: a comparative utilization and outcomes study. Clin Breast Cancer 16:319–326CrossRef
Metadata
Title
Management of the axilla in breast cancer: outcome analysis in a series of ductal versus lobular invasive cancers
Authors
S. P. Corona
M. Bortul
S. Scomersi
C. Bigal
C. Bottin
F. Zanconati
S. B. Fox
F. Giudici
D. Generali
Publication date
01-04-2020
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 3/2020
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-020-05565-x

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