Register for email alerts and news feeds:
This journal | BMJ Group
rss
Published Online First: 23 March 2006. doi:10.1136/jcp.2005.033043
Journal of Clinical Pathology 2006;59:729-735
Copyright © 2006 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists.

ORIGINAL ARTICLE

Basal-like breast carcinomas: clinical outcome and response to chemotherapy

S Banerjee1, J S Reis-Filho2,3, S Ashley4, D Steele2, A Ashworth2, S R Lakhani5 and I E Smith1

1 Breast Unit, Royal Marsden Hospital, London, UK
2 The Breakthough Breast Cancer Research Centre, Institute of Cancer Research, London
3 Life and Health Sciences Research Institute (ICVS), University of Minho, Braga, Portugal
4 Department of Computing, Royal Marsden Hospital, Sutton, UK
5 Molecular and Cellular Pathology, School of Medicine, The University of Queensland, Mayne Medical School, Herston, Australia

Correspondence to:
Correspondence to:
Professor I E Smith
Breast Unit, Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK; ian.smith{at}rmh.nhs.uk

Background: Grade-III invasive ductal carcinomas of no special type (IDCs-NST) constitute a heterogeneous group of tumours with different clinical behaviour and response to chemotherapy. As many as 25% of all grade-III IDCs-NST are known to harbour a basal-like phenotype, as defined by gene expression profiling or immunohistochemistry for basal cytokeratins. Patients with basal-like breast carcinomas (BLBC) are reported to have a shorter disease-free and overall survival.

Material and methods: A retrospective analysis of 49 patients with BLBC (as defined by basal cytokeratin expression) and 49 controls matched for age, nodal status and grade was carried out. Histological features, immunohistochemical findings for oestrogen receptor (ER), progesterone receptor (PgR) and HER2, and clinical outcome and survival after adjuvant chemotherapy were compared between the two groups.

Results: It was more likely for patients with BLBCs to be found negative for ER (p<0.0001), PgR (p<0.0001) and HER2 (p<0.01) than controls. Patients with BLBCs were found to have a significantly higher recurrence rate (p<0.05) and were associated with significantly shorter disease-free and overall survival (both p<0.05). In the group of patients who received anthracycline-based adjuvant chemotherapy (BLBC group, n = 47; controls, n = 49), both disease-free and overall survival were found to be significantly shorter in the BLBC group (p<0.05).

Conclusions: BLBCs are a distinct clinical and pathological entity, characterised by high nuclear grade, lack of hormone receptors and HER2 expression and a more aggressive clinical course. Standard adjuvant chemotherapy seems to be less effective in these tumours and new therapeutic approaches are indicated.

Abbreviations: BLBC, basal-like breast carcinoma; Ck, cytokeratin; EGFR, epidermal growth factor receptor; ER, oestrogen receptor; IDCs-NST, invasive ductal carcinomas of no special type; PgR, progesterone receptor


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Corkery, B., Crown, J., Clynes, M., O'Donovan, N. (2009). Epidermal growth factor receptor as a potential therapeutic target in triple-negative breast cancer. Ann Oncol 20: 862-867 [Abstract] [Full Text]  
  • Rakha, E. A., Elsheikh, S. E., Aleskandarany, M. A., Habashi, H. O., Green, A. R., Powe, D. G., El-Sayed, M. E., Benhasouna, A., Brunet, J.-S., Akslen, L. A., Evans, A. J., Blamey, R., Reis-Filho, J. S., Foulkes, W. D., Ellis, I. O. (2009). Triple-Negative Breast Cancer: Distinguishing between Basal and Nonbasal Subtypes. Clin. Cancer Res. 15: 2302-2310 [Abstract] [Full Text]  
  • Gobert, M., Treilleux, I., Bendriss-Vermare, N., Bachelot, T., Goddard-Leon, S., Arfi, V., Biota, C., Doffin, A. C., Durand, I., Olive, D., Perez, S., Pasqual, N., Faure, C., Ray-Coquard, I., Puisieux, A., Caux, C., Blay, J.-Y., Menetrier-Caux, C. (2009). Regulatory T Cells Recruited through CCL22/CCR4 Are Selectively Activated in Lymphoid Infiltrates Surrounding Primary Breast Tumors and Lead to an Adverse Clinical Outcome. Cancer Res. 69: 2000-2009 [Abstract] [Full Text]  
  • Cserni, G. (2008). Commentary on in-transit lymph node metastases in breast cancer: a possible source of local recurrence after Sentinel Node procedure. J. Clin. Pathol. 61: 1233-1235 [Full Text]  
  • Luck, A. A., Evans, A. J., James, J. J., Rakha, E. A., Paish, E. C., Green, A. R., Ellis, I. O. (2008). Breast Carcinoma with Basal Phenotype: Mammographic Findings. Am. J. Roentgenol. 191: 346-351 [Abstract] [Full Text]  
  • Walker, R A (2008). Immunohistochemical markers as predictive tools for breast cancer. J. Clin. Pathol. 61: 689-696 [Abstract] [Full Text]  
  • Rakha, E. A., Reis-Filho, J. S., Ellis, I. O. (2008). Basal-Like Breast Cancer: A Critical Review. JCO 26: 2568-2581 [Abstract] [Full Text]  
  • Korsching, E, Jeffrey, S S, Meinerz, W, Decker, T, Boecker, W, Buerger, H (2008). Basal carcinoma of the breast revisited: an old entity with new interpretations. J. Clin. Pathol. 61: 553-560 [Abstract] [Full Text]  
  • Eralp, Y., Derin, D., Ozluk, Y., Yavuz, E., Guney, N., Saip, P., Muslumanoglu, M., Igci, A., Kucucuk, S., Dincer, M., Aydiner, A., Topuz, E. (2008). MAPK overexpression is associated with anthracycline resistance and increased risk for recurrence in patients with triple-negative breast cancer. Ann Oncol 19: 669-674 [Abstract] [Full Text]  
  • Cheang, M. C.U., Voduc, D., Bajdik, C., Leung, S., McKinney, S., Chia, S. K., Perou, C. M., Nielsen, T. O. (2008). Basal-Like Breast Cancer Defined by Five Biomarkers Has Superior Prognostic Value than Triple-Negative Phenotype. Clin. Cancer Res. 14: 1368-1376 [Abstract] [Full Text]  
  • Winter, J. (2008). Morphological and immunophenotypic analysis of basal-like carcinoma of the breast. Bioscience Horizons 1: 19-27 [Abstract] [Full Text]  
  • Lu, S., Simin, K., Khan, A., Mercurio, A. M. (2008). Analysis of Integrin {beta}4 Expression in Human Breast Cancer: Association with Basal-like Tumors and Prognostic Significance. Clin. Cancer Res. 14: 1050-1058 [Abstract] [Full Text]  
  • Da Silva, L, Clarke, C, Lakhani, S R (2007). Demystifying basal-like breast carcinomas. J. Clin. Pathol. 60: 1328-1332 [Abstract] [Full Text]  
  • Wienke, D., Davies, G. C., Johnson, D. A., Sturge, J., Lambros, M. B.K., Savage, K., Elsheikh, S. E., Green, A. R., Ellis, I. O., Robertson, D., Reis-Filho, J. S., Isacke, C. M. (2007). The Collagen Receptor Endo180 (CD280) Is Expressed on Basal-like Breast Tumor Cells and Promotes Tumor Growth In vivo. Cancer Res. 67: 10230-10240 [Abstract] [Full Text]  
  • Altundag, K., Dede, D. S, Purnak, T. (2007). Albumin-bound paclitaxel (ABI-007; Abraxane) in the management of basal-like breast carcinoma. J. Clin. Pathol. 60: 958-958 [Full Text]  
  • Dent, R., Trudeau, M., Pritchard, K. I., Hanna, W. M., Kahn, H. K., Sawka, C. A., Lickley, L. A., Rawlinson, E., Sun, P., Narod, S. A. (2007). Triple-Negative Breast Cancer: Clinical Features and Patterns of Recurrence. Clin. Cancer Res. 13: 4429-4434 [Abstract] [Full Text]  
  • Verlinden, L., Vanden Bempt, I., Eelen, G., Drijkoningen, M., Verlinden, I., Marchal, K., De Wolf-Peeters, C., Christiaens, M.-R., Michiels, L., Bouillon, R., Verstuyf, A. (2007). The E2F-Regulated Gene Chk1 Is Highly Expressed in Triple-Negative Estrogen Receptor /Progesterone Receptor /HER-2 Breast Carcinomas. Cancer Res. 67: 6574-6581 [Abstract] [Full Text]  

eLetters:

Read all eLetters

Re: Basal-like breast carcinomas
Rosella Silvestrini
JCP Online, 12 Jun 2006 [Full text]

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Pathology jobs

Pathology jobs