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Lobular and non-lobular breast cancers differ regarding axillary lymph node metastasis: a cross-sectional study on 4,292 consecutive patients

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Abstract

Invasive lobular carcinoma (ILC) accounts for 8–14% of all breast cancers and carries distinct prognostic and biologic implications. The goal of our study was to investigate the impact of lobular histology on axillary lymph node (ALN) involvement. This is a cross-sectional study of 4,292 consecutive patients surgically treated for breast carcinoma at the University Hospitals Leuven. Logistic regression analysis was used to relate ILC to lymph node involvement while controlling for the following clinicopathologic features: tumor size, multifocal disease, tumor grade, lobular subtype and the combined steroid, and Her-2 status. Odds ratios (ORs) and 95% confidence intervals (CIS) were computed. A subgroup analysis was performed for patients that underwent a sentinel lymph node (SLN) procedure. The observed incidence of ILC was 13%. ILCs were larger, were more often grade II, multifocal, steroid receptor positive and Her-2 negative, and tended to be present in older patients. Incidence of ALN involvement was 42.0% for ILCs versus 38.3% for other tumors (OR 1.17, 95% CI 0.97–1.40). For the SLN subgroup, ILCs were less often ALN positive than non-ILCs (20.5% versus 28.3%, OR 0.66, 95% CI: 0.41–1.00). In the multivariable analysis, the lobular subtype was identified as less likely to have ALN involvement (adjusted OR 0.66, 95% CI 0.53–0.82). The analysis for the SLN subgroup showed comparable results (adjusted OR 0.49, 95% CI 0.30–0.78). This study has demonstrated that the lobular subtype is an independent predictor of lymph node involvement with ILC having a lower incidence of involved lymph nodes. The mildly higher incidence of ALN metastasis in lobular cancers in univariable analysis is not due to the lobular subtype, but due to confounding factors that interact with lymph node involvement.

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References

  1. Patani NR, Dwek MV, Douek M (2007) Predictors of axillary lymph node metastasis in breast cancer: a systematic review. Eur J Surg Oncol 33(4):409–419

    PubMed  CAS  Google Scholar 

  2. Arpino G, Bardou VJ, Clark GM, Elledge RM (2004) Infiltrating lobular carcinoma of the breast: tumor characteristics and clinical outcome. Breast Cancer Res 6(3):R149–R156

    Article  PubMed  Google Scholar 

  3. Cristofanilli M, Gonzalez-Angulo A, Sneige N, Kau SW, Broglio K, Theriault RL, Valero V, Buzdar AU, Kuerer H, Buccholz TA et al (2005) Invasive lobular carcinoma classic type: response to primary chemotherapy and survival outcomes. J Clin Oncol 23(1):41–48

    Article  PubMed  Google Scholar 

  4. Pestalozzi BC, Zahrieh D, Mallon E, Gusterson BA, Price KN, Gelber RD, Holmberg SB, Lindtner J, Snyder R, Thurlimann B et al (2008) Distinct clinical and prognostic features of infiltrating lobular carcinoma of the breast: combined results of 15 International Breast Cancer Study Group clinical trials. J Clin Oncol 26(18):3006–3014

    Article  PubMed  Google Scholar 

  5. Tubiana-Hulin M, Stevens D, Lasry S, Guinebretiere JM, Bouita L, Cohen-Solal C, Cherel P, Rouesse J (2006) Response to neoadjuvant chemotherapy in lobular and ductal breast carcinomas: a retrospective study on 860 patients from one institution. Ann Oncol 17(8):1228–1233

    Article  PubMed  CAS  Google Scholar 

  6. Viale G, Zurrida S, Maiorano E, Mazzarol G, Pruneri G, Paganelli G, Maisonneuve P, Veronesi U (2005) Predicting the status of axillary sentinel lymph nodes in 4351 patients with invasive breast carcinoma treated in a single institution. Cancer 103(3):492–500

    Article  PubMed  Google Scholar 

  7. Wasif N, Maggard MA, Ko CY, Giuliano AE (2010) Invasive lobular vs. ductal breast cancer: a stage-matched comparison of outcomes. Ann Surg Oncol 17(7):1862–1869

    Article  PubMed  Google Scholar 

  8. Neven P, Van Calster B, Van den Bempt I, Van Huffel S, Van Belle V, Hendrickx W, Decock J, Wildiers H, Paridaens R, Amant F et al (2008) Age interacts with the expression of steroid and HER-2 receptors in operable invasive breast cancer. Breast Cancer Res Treat 110(1):153–159

    Article  PubMed  CAS  Google Scholar 

  9. Hastie T, Tibshirani R (1990) Generalized additive models, 1st edn. Chapman and Hall, London; New York

    Google Scholar 

  10. Tubiana M (1998) Benefits and limitations of mass screening. The natural history of breast cancer. Bull Acad Natl Med 182(8):1593–1610 discussion 1610-1591

    PubMed  CAS  Google Scholar 

  11. Bevilacqua JL, Kattan MW, Fey JV, Cody HS III, Borgen PI, Van Zee KJ (2007) Doctor, what are my chances of having a positive sentinel node? A validated nomogram for risk estimation. J Clin Oncol 25(24):3670–3679

    Article  PubMed  Google Scholar 

  12. Voogd AC, Repelaer van Driel OJ, Roumen RM, Crommelin MA, van Beek MW, Coebergh JW (1997) Changing attitudes towards breast-conserving treatment of early breast cancer in the south-eastern Netherlands: results of a survey among surgeons and a registry-based analysis of patterns of care. Eur J Surg Oncol 23(2):134–138

    Article  PubMed  CAS  Google Scholar 

  13. Gann PH, Colilla SA, Gapstur SM, Winchester DJ, Winchester DP (1999) Factors associated with axillary lymph node metastasis from breast carcinoma: descriptive and predictive analyses. Cancer 86(8):1511–1519

    Article  PubMed  CAS  Google Scholar 

  14. Olivotto IA, Jackson JS, Mates D, Andersen S, Davidson W, Bryce CJ, Ragaz J (1998) Prediction of axillary lymph node involvement of women with invasive breast carcinoma: a multivariate analysis. Cancer 83(5):948–955

    Article  PubMed  CAS  Google Scholar 

  15. Velanovich V, Szymanski W (1998) Lymph node metastasis in breast cancer: common prognostic markers lack predictive value. Ann Surg Oncol 5(7):613–619

    Article  PubMed  CAS  Google Scholar 

  16. Voogd AC, Coebergh JW, Repelaer van Driel OJ, Roumen RM, van Beek MW, Vreugdenhil A, Crommelin MA (2000) The risk of nodal metastases in breast cancer patients with clinically negative lymph nodes: a population-based analysis. Breast Cancer Res Treat 62(1):63–69

    Article  PubMed  CAS  Google Scholar 

  17. Sastre-Garau X, Jouve M, Asselain B, Vincent-Salomon A, Beuzeboc P, Dorval T, Durand JC, Fourquet A, Pouillart P (1996) Infiltrating lobular carcinoma of the breast. Clinicopathologic analysis of 975 cases with reference to data on conservative therapy and metastatic patterns. Cancer 77(1):113–120

    Article  PubMed  CAS  Google Scholar 

  18. Cserni G (2006) Histopathologic examination of the sentinel lymph nodes. Breast J 12(5 Suppl 2):S152–S156

    Article  PubMed  Google Scholar 

  19. Patil DT, Susnik B (2008) Keratin immunohistochemistry does not contribute to correct lymph node staging in patients with invasive lobular carcinoma. Hum Pathol 39(7):1011–1017

    Article  PubMed  CAS  Google Scholar 

  20. Maiorano E, Regan MM, Viale G, Mastropasqua MG, Colleoni M, Castiglione-Gertsch M, Price KN, Gelber RD, Goldhirsch A, Coates AS (2010) Prognostic and predictive impact of central necrosis and fibrosis in early breast cancer: results from two International Breast Cancer Study Group randomized trials of chemoendocrine adjuvant therapy. Breast Cancer Res Treat 121(1):211–218

    Article  PubMed  Google Scholar 

  21. Zurrida S, Morabito A, Galimberti V, Luini A, Greco M, Bartoli C, Raselli R, Rossi N, Vessecchia G, Cascinelli N et al (1999) Importance of the level of axillary involvement in relation to traditional variables in the prognosis of breast cancer. Int J Oncol 15(3):475–480

    PubMed  CAS  Google Scholar 

  22. Da Silva L, Parry S, Reid L, Keith P, Waddell N, Kossai M, Clarke C, Lakhani SR, Simpson PT (2008) Aberrant expression of E-cadherin in lobular carcinomas of the breast. Am J Surg Pathol 32(5):773–783

    Article  PubMed  Google Scholar 

  23. Rakha EA, Abd El Rehim D, Pinder SE, Lewis SA, Ellis IO (2005) E-cadherin expression in invasive non-lobular carcinoma of the breast and its prognostic significance. Histopathology 46(6):685–693

    Article  PubMed  CAS  Google Scholar 

  24. Michaelson JS, Silverstein M, Wyatt J, Weber G, Moore R, Halpern E, Kopans DB, Hughes K (2002) Predicting the survival of patients with breast carcinoma using tumor size. Cancer 95(4):713–723

    Article  PubMed  Google Scholar 

  25. Verkooijen HM, Fioretta G, Vlastos G, Morabia A, Schubert H, Sappino AP, Pelte MF, Schafer P, Kurtz J, Bouchardy C (2003) Important increase of invasive lobular breast cancer incidence in Geneva, Switzerland. Int J Cancer 104(6):778–781

    Article  PubMed  CAS  Google Scholar 

  26. Dixon AR, Ellis IO, Elston CW, Blamey RW (1991) A comparison of the clinical metastatic patterns of invasive lobular and ductal carcinomas of the breast. Br J Cancer 63(4):634–635

    Article  PubMed  CAS  Google Scholar 

  27. Gudlaugsson E, Skaland I, Janssen EA, van Diest PJ, Voorhorst FJ, Kjellevold K, zur Hausen A, Baak JP (2010) Prospective multicenter comparison of proliferation and other prognostic factors in lymph node negative lobular invasive breast cancer. Breast Cancer Res Treat 121(1):35–40

    Article  PubMed  CAS  Google Scholar 

  28. Toikkanen S, Pylkkanen L, Joensuu H (1997) Invasive lobular carcinoma of the breast has better short- and long-term survival than invasive ductal carcinoma. Br J Cancer 6(9):1234–1240

    Article  Google Scholar 

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Acknowledgments

BVC is a postdoctoral fellow of the Research Foundation—Flanders (FWO). KVH is supported by a grant from the Agency for Innovation by Science and Technology (IWT).

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Correspondence to A. Smeets.

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T. Vandorpe and A. Smeets contributed equally in this study.

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Vandorpe, T., Smeets, A., Van Calster, B. et al. Lobular and non-lobular breast cancers differ regarding axillary lymph node metastasis: a cross-sectional study on 4,292 consecutive patients. Breast Cancer Res Treat 128, 429–435 (2011). https://doi.org/10.1007/s10549-011-1565-4

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  • DOI: https://doi.org/10.1007/s10549-011-1565-4

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