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Old 04-26-2006, 01:14 PM   #1
Lani
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Effectiveness of tamoxifen related to ER, PR, HER2, EGFR status

Benefit of tamoxifen even in ER- pts if PR+! Her2+ patients tend to be tamoxifen resistant (but small number of pts in this study)

ABSTRACT: Benefit from adjuvant tamoxifen therapy in primary breast cancer patients according oestrogen receptor, progesterone receptor, EGF receptor and HER2 status [Annals of Oncology; Subscribe; Sample]
Background: Most women with oestrogen receptor (ER) positive primary breast cancer receive adjuvant tamoxifen after surgery. The measurement of tumour biomarkers should allow better selection of patients for such treatment or for therapies such as aromatase inhibitors.

Patients and methods: Histopathological blocks of primary breast cancer patients who had been randomized to receive 2-years tamoxifen or no adjuvant therapy in two mature randomised clinical trials were retrieved. Immunohistochemical staining for ER, progesterone receptor (PgR), HER2 and epidermal growth factor receptor (EGFR) was undertaken. The primary endpoint was relapse free survival.

Results: 813 patients were included in the study. Benefit from tamoxifen was seen in ER-positive patients [Relative risk (rr) 0.77, ci 0.63-0.93]. ER-negative patients also showed a strong trend to benefit from tamoxifen (rr 0.73, ci 0.52-1.02) which was largely confined to the PgR-positive group. Amongst the ER-positive group, PgR-positive and PgR-negative patients showed similar benefit (rr 0.81; ci 0.65-1.02 and 0.70; ci 0.49-0.99, respectively). Patients positive for HER2 did not benefit significantly (rr 1.14; ci 0.75-1.73) but this group was small.

Conclusions: Measurement of PgR status in ER-negative patients defines a group of patients that benefit from tamoxifen but would be excluded from tamoxifen therapy on the basis of ER status alone. The data are consistent with HER2 positive tumours being resistant to tamoxifen.
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Old 04-26-2006, 09:52 PM   #2
Rozebud
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Interesting study, particularly for those er- pr+ like myself. Can you send a link to the whole article and date? Thanks!!
__________________
Rose

Dx'd 1/04 at 33, while 33 weeks pregnant

Dx: Stage IIIC IDC, ER-, PR+ (23%), Her2=2.7 (IDC)/7.6 (FSH), 2.5cm primary tumor, grade III, 11/18+ nodes (largest 3.8 cm)

Treatment: A/C *4, T *4, 1 year of herceptin (BCIRG 006), mastectomy, rads (7 weeks), zoladex (5 years) with tamoxifen (2 years)/aromisin (3 years), bilateral SGAP summer 05 at NOLA

Oops, retested tumor and I guess I'm er/pr- after all.
Stopped all hormonal tx 10/07. Periods resumed 6/08. Bye bye hot flashes!!!!

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Old 04-27-2006, 03:13 AM   #3
Lani
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article

Mitch Dowsett and Michael Baum seem to be two of the foremost researchers specializing in the hormonal treatment of cancer--Here it is:


Annals of Oncology Advance Access originally published online on February 23, 2006
Annals of Oncology 2006 17(5):818-826; doi:10.1093/annonc/mdl016

Benefit from adjuvant tamoxifen therapy in primary breast cancer patients according oestrogen receptor, progesterone receptor, EGF receptor and HER2 status

M. Dowsett1,*, J. Houghton2, C. Iden2, J. Salter1, J. Farndon3, R. A'Hern4, R. Sainsbury5 and M. Baum6
1 Academic Department of Biochemistry, The Royal Marsden NHS Trust, London; 2 Clinical Trials Group of the Department of Surgery, Royal Free and University College Medical School, University College London, London; 3 University Department of Surgery, Bristol Royal Infirmary, Bristol; 4 Clinical Trials and Statistics Unit, Institute of Cancer Research, Sutton, Surrey; 5 Department of Surgery, University College, London; 6 The Portland Hospital, London, UK
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