Please use this identifier to cite or link to this item: http://hdl.handle.net/1959.13/43333
- Title
- Relationship between quantitative estrogen and progesterone receptor expression and human epidermal growth factor receptor 2 (HER-2) status with recurrence in the arimidex, tamoxifen, alone or in combination trial
- Author/Creator
-
Dowsett, Mitch;
Allred, Craig;
Bishop, Hugh;
Ellis, Ian;
Larsimont, Danis;
Sasano, Hironobu;
Carder, Pauline;
Cussac, Antonio L.;
Knox, Fiona;
Speirs, Valerie;
Forbes, John;
Buzdar, Aman;
Knox, Jill;
Quinn, Emma;
Salter, Janine;
Wale, Chris;
Cuzick, Jack;
Houghton, Joan;
Williams, Norman;
Mallon, Elizabeth
- Institution
- The University of Newcastle. Faculty of Health, School of Medicine and Public Health
- Description
- Purpose: To determine the relationship between quantitative estrogen-receptor (ER) and progesterone-receptor (PgR) expression and human epidermal growth factor 2 (HER-2) status with time to recurrence (TTR) in postmenopausal women with hormone receptor–positive primary breast cancer treated with anastrozole or tamoxifen as adjuvant therapy. Patients and Methods: Formalin-fixed, paraffin-embedded tumor blocks were retrospectively collected from patients in the monotherapy arms of the Arimidex, Tamoxifen Alone or in Combination (ATAC) trial and centrally tested for ER, PgR and HER-2. ER and PgR were scored using continuous scales and HER-2 was scored as 0 to 3+ with 2+ cases being analyzed by fluorescence in situ hybridization. Results: Blocks were collected from 2,006 of 5,880 eligible patients. Tissue was assessable and ER and/or PgR positivity confirmed centrally in 1,782 cases. In these, TTR was longer for anastrozole than for tamoxifen by a similar extent to that in the overall trial. None of the three biomarkers identified a set of patients with differential benefit from anastrozole over tamoxifen. Patients with low ER, low PgR, and high HER-2 expression had a poorer prognosis with either drug. Only 2.6% of patients in the highest quartile of PgR experienced recurrence after 5 years, compared with 13.2% in the lowest quartile. Conclusion: Quantitative expression of ER and PgR and HER-2 status did not identify patients with differential relative benefit from anastrozole over tamoxifen: TTR was longer for anastrozole than for tamoxifen in all molecular subgroups. Low ER or PgR or high HER-2 expression are associated with a high risk of recurrence with either anastrozole or tamoxifen.
- Relation
- Journal of Clinical Oncology Vol. 26, Issue 7, p. 1059-1065
- Publisher Link
- http://dx.doi.org/10.1200/JCO.2007.12.9437
- Date
- 2008
- Publisher
- American Society of Clinical Oncology
- Keyword(s)
-
estrogen-receptor;
progesterone-receptor;
human epidermal growth factor 2 (HER-2);
time to recurrence;
postmenopausal women;
tamoxifen;
anastrozole
- Resource Type
- journal article
- Identifier
- http://hdl.handle.net/1959.13/43333
- Identifier
- ISSN:0732-183X
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