Literature DB >> 11689582

Influence of endocrine-related factors on response to perioperative chemotherapy for patients with node-negative breast cancer.

M Colleoni1, S Gelber, A S Coates, M Castiglione-Gertsch, R D Gelber, K Price, C M Rudenstam, J Lindtner, J Collins, B Thürlimann, S B Holmberg, H Cortes-Funes, E Simoncini, E Murray, M Fey, A Goldhirsch.   

Abstract

PURPOSE: We investigated tumor- and patient-related features that might influence the response to perioperative chemotherapy (PeCT) compared with no adjuvant therapy for patients with node-negative breast cancer. PATIENTS AND METHODS: A total of 1,275 patients were randomized to either no adjuvant treatment (427 patients) or PeCT (848 patients). The following variables thought to have prognostic significance were evaluated: grade, tumor size, estrogen (ER) and progesterone receptor (PgR) content (absent; low, 1 to 9 fmol/mg cytosol protein; or positive, > or = 10 fmol/mg cytosol protein), c-erbB-2 overexpression, menopausal status, and age. Cox proportional hazards regression models were used to assess the relative influence of these factors to predict the effect of PeCT on disease-free survival (DFS). Median follow-up was 13.5 years.
RESULTS: The 10-year DFS percentage for 692 premenopausal patients did not significantly differ between the PeCT and no-adjuvant-treatment groups: 61% and 59%, respectively (relative risk [RR], 0.95; 95% confidence interval [CI], 0.75 to 1.20; P = .70). No predictive factors were identified. For 583 postmenopausal patients, 10-year DFS percentages for the groups were 63% and 58%, respectively (RR, 0.75; 95% CI, 0.58 to 0.93; P = .03). The absence of expression of ER, PgR, or both ER and PgR was the most important factor predicting improved outcome with PeCT among postmenopausal patients. The 10-year DFS percentages were 85% and 53% for the steroid hormone receptor-absent cohort of treated and untreated patients, respectively (RR, 0.18; 95% CI, 0.06 to 0.49; P = .0009).
CONCLUSION: The role of PeCT should be explored for patients whose primary tumors do not express steroid hormone receptors, because it is likely that early initiation of treatment is exclusively relevant for such patients.

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Year:  2001        PMID: 11689582     DOI: 10.1200/JCO.2001.19.21.4141

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  10 in total

Review 1.  Endocrine Therapy in the Current Management of Postmenopausal Estrogen Receptor-Positive Metastatic Breast Cancer.

Authors:  Virginia G Kaklamani; William J Gradishar
Journal:  Oncologist       Date:  2017-03-17

2.  Prognosis of medullary breast cancer: analysis of 13 International Breast Cancer Study Group (IBCSG) trials.

Authors:  J Huober; S Gelber; A Goldhirsch; A S Coates; G Viale; C Öhlschlegel; K N Price; R D Gelber; M M Regan; B Thürlimann
Journal:  Ann Oncol       Date:  2012-06-14       Impact factor: 32.976

3.  Challenges of treating incidental synchronous bilateral breast cancer with differing tumour biology.

Authors:  Jonathan Walter Esclovon; Melissa Ponder; Nail Aydin; Subhasis Misra
Journal:  BMJ Case Rep       Date:  2016-08-18

4.  Predictive value and clinical utility of centrally assessed ER, PgR, and Ki-67 to select adjuvant endocrine therapy for premenopausal women with hormone receptor-positive, HER2-negative early breast cancer: TEXT and SOFT trials.

Authors:  Meredith M Regan; Olivia Pagani; Prudence A Francis; Gini F Fleming; Barbara A Walley; Roswitha Kammler; Patrizia Dell'Orto; Leila Russo; János Szőke; Franco Doimi; Laura Villani; Stefano Pizzolitto; Christian Öhlschlegel; Fausto Sessa; Vicente Peg Cámara; José Luis Rodríguez Peralto; Gaëtan MacGrogan; Marco Colleoni; Aron Goldhirsch; Karen N Price; Alan S Coates; Richard D Gelber; Giuseppe Viale
Journal:  Breast Cancer Res Treat       Date:  2015-10-22       Impact factor: 4.872

5.  Distinct mechanisms of resistance to fulvestrant treatment dictate level of ER independence and selective response to CDK inhibitors in metastatic breast cancer.

Authors:  Kamila Kaminska; Nina Akrap; Ana Bosch; Gabriella Honeth; Johan Staaf; Carla L Alves; Anna Ehinger; Anna Ebbesson; Ingrid Hedenfalk; Lukas Beumers; Srinivas Veerla; Katja Harbst; Sidse Ehmsen; Signe Borgquist; Åke Borg; Alejandro Pérez-Fidalgo; Henrik J Ditzel
Journal:  Breast Cancer Res       Date:  2021-02-18       Impact factor: 6.466

6.  Nafamostat mesylate overcomes endocrine resistance of breast cancer through epigenetic regulation of CDK4 and CDK6 expression.

Authors:  Yueh-Te Lin; Joseph Lin; Yi-En Liu; Kai-Wen Hsu; Chang-Chi Hsieh; Dar-Ren Chen; Han-Tsang Wu
Journal:  Transl Oncol       Date:  2021-12-07       Impact factor: 4.243

7.  New and emerging treatments for estrogen receptor-positive breast cancer: focus on everolimus.

Authors:  Elisavet Paplomata; Ruth O'Regan
Journal:  Ther Clin Risk Manag       Date:  2013-01-14       Impact factor: 2.423

8.  Factors that predict early treatment failure for patients with locally advanced (T4) breast cancer.

Authors:  E Montagna; V Bagnardi; N Rotmensz; J Rodriguez; P Veronesi; A Luini; M Intra; E Scarano; A Cardillo; R Torrisi; G Viale; A Goldhirsch; M Colleoni
Journal:  Br J Cancer       Date:  2008-05-27       Impact factor: 7.640

9.  Inhibition of ERα/ERK/P62 cascades induces "autophagic switch" in the estrogen receptor-positive breast cancer cells exposed to gemcitabine.

Authors:  Peng Shen; Ming Chen; Mengye He; Luoquan Chen; Yinjing Song; Peng Xiao; Xiaopeng Wan; Feng Dai; Ting Pan; Qingqing Wang
Journal:  Oncotarget       Date:  2016-07-26

Review 10.  My burning issues in the neoadjuvant treatment for breast cancer.

Authors:  Elisabeth S Bergen; Rupert Bartsch
Journal:  Memo       Date:  2017-12-22
  10 in total

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