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Published in: Breast Cancer Research and Treatment 2/2009

01-09-2009 | Clinical Trial

Patterns of recurrence of early breast cancer according to estrogen receptor status: a therapeutic target for a quarter of a century

Authors: Olivia Pagani, Karen N. Price, Richard D. Gelber, Monica Castiglione-Gertsch, Stig B. Holmberg, Jurij Lindtner, Beat Thürlimann, John Collins, Martin F. Fey, Alan S. Coates, Aron Goldhirsch, International Breast Cancer Study Group (IBCSG)

Published in: Breast Cancer Research and Treatment | Issue 2/2009

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Abstract

The current therapeutic strategy in breast cancer is to identify a target, such as estrogen receptor (ER) status, for tailoring treatments. We investigated the patterns of recurrence with respect to ER status for patients treated in two randomized trials with 25 years’ median follow-up. In the ER-negative subpopulations most breast cancer events occurred within the first 5–7 years after randomization, while in the ER-positive subpopulations breast cancer events were spread through 10 years. In the ER-positive subpopulation, 1 year endocrine treatment alone significantly prolonged disease-free survival (DFS) with no additional benefit observed by adding 1 year of chemotherapy. In the small ER-negative subpopulation chemo-endocrine therapy had a significantly better DFS than endocrine alone or no treatment. Despite small numbers of patients, “old-fashioned” treatments, and competing causes of treatment failure, the value of ER status as a target for response to adjuvant treatment is evident through prolonged follow-up.
Literature
1.
2.
5.
go back to reference Early Breast Cancer Trialists’ Collaborative Group (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717. doi:10.1016/S0140-6736(05)66544-0 CrossRef Early Breast Cancer Trialists’ Collaborative Group (2005) Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet 365:1687–1717. doi:10.​1016/​S0140-6736(05)66544-0 CrossRef
6.
go back to reference Ludwig Breast Cancer Study Group (1984) Randomized trial of chemoendocrine therapy, endocrine therapy, and mastectomy alone in postmenopausal patients with operable breast cancer and axillary node metastasis. Lancet 1:1256–1260 Ludwig Breast Cancer Study Group (1984) Randomized trial of chemoendocrine therapy, endocrine therapy, and mastectomy alone in postmenopausal patients with operable breast cancer and axillary node metastasis. Lancet 1:1256–1260
7.
go back to reference Goldhirsch A, Gelber RD, Simes RJ et al (1989) Costs and benefits of adjuvant therapy in breast cancer: a quality-adjusted survival analysis. J Clin Oncol 7:36–44PubMed Goldhirsch A, Gelber RD, Simes RJ et al (1989) Costs and benefits of adjuvant therapy in breast cancer: a quality-adjusted survival analysis. J Clin Oncol 7:36–44PubMed
8.
go back to reference Castiglione M, Gelber RD, Goldhirsch A (1990) Adjuvant systemic therapy for breast cancer in the elderly: competing causes of mortality. J Clin Oncol 8:519–526PubMed Castiglione M, Gelber RD, Goldhirsch A (1990) Adjuvant systemic therapy for breast cancer in the elderly: competing causes of mortality. J Clin Oncol 8:519–526PubMed
9.
go back to reference Castiglione-Gertsch M, Johnsen C, Goldhirsch A et al (1994) The International (Ludwig) Breast Cancer Study Group Trials I–IV: 15 years follow-up. Ann Oncol 5:717–724PubMed Castiglione-Gertsch M, Johnsen C, Goldhirsch A et al (1994) The International (Ludwig) Breast Cancer Study Group Trials I–IV: 15 years follow-up. Ann Oncol 5:717–724PubMed
10.
go back to reference Crivellari D, Price K, Gelber RD et al (2003) Adjuvant endocrine therapy compared with no systemic therapy for elderly women with early breast cancer: 21-year results of International Breast Cancer Study Group Trial IV. J Clin Oncol 21:4517–4523. doi:10.1200/JCO.2003.03.559 PubMedCrossRef Crivellari D, Price K, Gelber RD et al (2003) Adjuvant endocrine therapy compared with no systemic therapy for elderly women with early breast cancer: 21-year results of International Breast Cancer Study Group Trial IV. J Clin Oncol 21:4517–4523. doi:10.​1200/​JCO.​2003.​03.​559 PubMedCrossRef
13.
go back to reference Kalbfleisch JD, Prentice RL (1980) The statistical analysis of failure time data. Wiley, New York, p 169 Kalbfleisch JD, Prentice RL (1980) The statistical analysis of failure time data. Wiley, New York, p 169
14.
go back to reference Saphner T, Tormey DC, Gray R (1996) Annual hazard rates of recurrence for breast cancer after primary therapy. J Clin Oncol 14:2738–2746PubMed Saphner T, Tormey DC, Gray R (1996) Annual hazard rates of recurrence for breast cancer after primary therapy. J Clin Oncol 14:2738–2746PubMed
15.
go back to reference Goss P, Allan AL, Rodenhiser DI et al (2008) New clinical and experimental approaches for studying tumour dormancy: does tumour dormancy offer a therapeutic target? APMIS 116:552–568PubMed Goss P, Allan AL, Rodenhiser DI et al (2008) New clinical and experimental approaches for studying tumour dormancy: does tumour dormancy offer a therapeutic target? APMIS 116:552–568PubMed
16.
go back to reference Clough-Gorr KM, Fink AK, Silliman RA (2008) Challenges associated with longitudinal survivorship research: attrition and a novel approach of reenrollment in a 6-year follow-up study of older breast cancer survivors. J Cancer Surviv 2(2):95–103. doi:10.1007/s11764-008-0049-y PubMedCrossRef Clough-Gorr KM, Fink AK, Silliman RA (2008) Challenges associated with longitudinal survivorship research: attrition and a novel approach of reenrollment in a 6-year follow-up study of older breast cancer survivors. J Cancer Surviv 2(2):95–103. doi:10.​1007/​s11764-008-0049-y PubMedCrossRef
17.
go back to reference Cufer T (2007) Reducing the risk for breast cancer recurrence after completion of tamoxifen treatment in postmenopausal women. Ann Oncol Suppl 8:viii8–viii17 Cufer T (2007) Reducing the risk for breast cancer recurrence after completion of tamoxifen treatment in postmenopausal women. Ann Oncol Suppl 8:viii8–viii17
20.
go back to reference Albain K, Barlow W, O’Malley F et al (2004) Mature outcomes and new biologic correlates on phase III Intergroup trial 0100 (INT-0100, SWOG-8814): concurrent (CAFT) vs sequential (CAF-T) chemohormonal therapy (cyclophosphamide, doxorubicin, 5-fluorouracil, tamoxifen) vs T alone for postmenopausal, node positive, estrogen (ER) and/or progesterone PgR receptor-positive breast cancer. Proc San Antonio Breast Cancer Symposium, 2004 (Abstr 37) Albain K, Barlow W, O’Malley F et al (2004) Mature outcomes and new biologic correlates on phase III Intergroup trial 0100 (INT-0100, SWOG-8814): concurrent (CAFT) vs sequential (CAF-T) chemohormonal therapy (cyclophosphamide, doxorubicin, 5-fluorouracil, tamoxifen) vs T alone for postmenopausal, node positive, estrogen (ER) and/or progesterone PgR receptor-positive breast cancer. Proc San Antonio Breast Cancer Symposium, 2004 (Abstr 37)
Metadata
Title
Patterns of recurrence of early breast cancer according to estrogen receptor status: a therapeutic target for a quarter of a century
Authors
Olivia Pagani
Karen N. Price
Richard D. Gelber
Monica Castiglione-Gertsch
Stig B. Holmberg
Jurij Lindtner
Beat Thürlimann
John Collins
Martin F. Fey
Alan S. Coates
Aron Goldhirsch
International Breast Cancer Study Group (IBCSG)
Publication date
01-09-2009
Publisher
Springer US
Published in
Breast Cancer Research and Treatment / Issue 2/2009
Print ISSN: 0167-6806
Electronic ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-008-0282-0

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