Literature DB >> 15027887

The interaction of oestrogen receptor status and pathological features with adjuvant treatment in relation to survival in patients with operable breast cancer: a retrospective study of 2660 patients.

D M Barnes1, R R Millis, C E Gillett, K Ryder, D Skilton, I S Fentiman, R D Rubens.   

Abstract

The oestrogen receptor (ER) status of 2660 patients with primary breast cancer has been related to the effect of different adjuvant systemic therapies on survival. However, as patients in the various treatment groups also had different prognostic features comparison between treatments was difficult. Over 90% of patients receiving tamoxifen (Tam) were postmenopausal compared with <20% of those receiving chemotherapy (CT). The latter had more positive nodes (85% vs 54%) and grade III tumours (54% vs 30%) than the Tam group. The combined CT and Tam group had similar characteristics to the CT alone group. The current reported increase in the proportion of women with ER+ tumours is explained by immunohistochemical analysis of ER and screening programmes. ER status was unrelated to survival in patients with small, low grade, node-negative tumours which was no different from that expected for age-matched women taken from the general population. The value of adjuvant treatment in these patients is therefore questionable. In those given any adjuvant treatment, survival of women with ER+ tumours was prolonged, with the greatest effect being seen in those receiving Tam. Patients with ER- tumours benefited from CT but the addition of Tam to CT improved survival only in those with ER+ tumours. ER status is now established as a major predictive factor for treatment selection in primary disease. Studies of prognostic and predictive markers may be invalidated by use of adjuvant therapy and selection criteria for different treatments. Survival will be influenced by both tumour biology and therapy. This important consideration must be remembered when analysing new markers, particularly in small studies.

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Year:  2004        PMID: 15027887     DOI: 10.1677/erc.0.0110085

Source DB:  PubMed          Journal:  Endocr Relat Cancer        ISSN: 1351-0088            Impact factor:   5.678


  7 in total

1.  Suppressor of cytokine signalling 2 (SOCS-2) expression in breast carcinoma.

Authors:  F Farabegoli; C Ceccarelli; D Santini; M Taffurelli
Journal:  J Clin Pathol       Date:  2005-10       Impact factor: 3.411

2.  A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH.

Authors:  R Roylance; P Gorman; T Papior; Y-L Wan; M Ives; J E Watson; C Collins; N Wortham; C Langford; H Fiegler; N Carter; C Gillett; P Sasieni; S Pinder; A Hanby; I Tomlinson
Journal:  Oncogene       Date:  2006-05-15       Impact factor: 9.867

3.  Improved surgical outcomes for breast cancer patients receiving neoadjuvant aromatase inhibitor therapy: results from a multicenter phase II trial.

Authors:  John A Olson; G Thomas Budd; Lisa A Carey; Lyndsay A Harris; Laura J Esserman; Gini F Fleming; Paul K Marcom; George S Leight; Therese Giuntoli; Paul Commean; Kyongtae Bae; Jingqin Luo; Matthew J Ellis
Journal:  J Am Coll Surg       Date:  2009-05       Impact factor: 6.113

4.  Tumor angiogenesis: pericytes and maturation are not to be ignored.

Authors:  Elham Fakhrejahani; Masakazu Toi
Journal:  J Oncol       Date:  2011-10-09       Impact factor: 4.375

Review 5.  Precision Medicine in Hormone Receptor-Positive Breast Cancer.

Authors:  Azadeh Nasrazadani; Roby A Thomas; Steffi Oesterreich; Adrian V Lee
Journal:  Front Oncol       Date:  2018-05-04       Impact factor: 6.244

6.  Exomes of Ductal Luminal Breast Cancer Patients from Southwest Colombia: Gene Mutational Profile and Related Expression Alterations.

Authors:  Carolina Cortes-Urrea; Fernando Bueno-Gutiérrez; Melissa Solarte; Miguel Guevara-Burbano; Fabian Tobar-Tosse; Patricia E Vélez-Varela; Juan Carlos Bonilla; Guillermo Barreto; Jaime Velasco-Medina; Pedro A Moreno; Javier De Las Rivas
Journal:  Biomolecules       Date:  2020-04-30

7.  Induction of ErbB-3 expression by alpha6beta4 integrin contributes to tamoxifen resistance in ERbeta1-negative breast carcinomas.

Authors:  Valentina Folgiero; Paolo Avetrani; Giulia Bon; Selene E Di Carlo; Alessandra Fabi; Cecilia Nisticò; Patrizia Vici; Elisa Melucci; Simonetta Buglioni; Letizia Perracchio; Isabella Sperduti; Laura Rosanò; Ada Sacchi; Marcella Mottolese; Rita Falcioni
Journal:  PLoS One       Date:  2008-02-13       Impact factor: 3.240

  7 in total

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