Long-term outcome and prognostic value of Ki67 after perioperative endocrine therapy in postmenopausal women with hormone-sensitive early breast cancer (POETIC): an open-label, multicentre, parallel-group, randomised, phase 3 trial.


Journal

The Lancet. Oncology
ISSN: 1474-5488
Titre abrégé: Lancet Oncol
Pays: England
ID NLM: 100957246

Informations de publication

Date de publication:
11 2020
Historique:
received: 07 04 2020
revised: 16 07 2020
accepted: 16 07 2020
entrez: 5 11 2020
pubmed: 6 11 2020
medline: 26 11 2020
Statut: ppublish

Résumé

Preoperative and perioperative aromatase inhibitor (POAI) therapy has the potential to improve outcomes in women with operable oestrogen receptor-positive primary breast cancer. It has also been suggested that tumour Ki67 values after 2 weeks (Ki67 POETIC was an open-label, multicentre, parallel-group, randomised, phase 3 trial (done in 130 UK hospitals) in which postmenopausal women aged at least 50 years with WHO performance status 0-1 and hormone receptor-positive, operable breast cancer were randomly assigned (2:1) to POAI (letrozole 2·5 mg per day orally or anastrozole 1 mg per day orally) for 14 days before and following surgery or no POAI (control). Adjuvant treatment was given as per UK standard local practice. Randomisation was done centrally by computer-generated permuted block method (variable block size of six or nine) and was stratified by hospital. Treatment allocation was not masked. The primary endpoint was time to recurrence. A key second objective explored association between Ki67 (dichotomised at 10%) and disease outcomes. The primary analysis for clinical endpoints was by modified intention to treat (excluding patients who withdrew consent). For Ki67 biomarker association and endpoint analysis, the evaluable population included all randomly assigned patients who had paired Ki67 values available. This study is registered with ClinicalTrials.gov, NCT02338310; the European Clinical Trials database, EudraCT2007-003877-21; and the ISRCTN registry, ISRCTN63882543. Recruitment is complete and long-term follow-up is ongoing. Between Oct 13, 2008, and April 16, 2014, 4480 women were recruited and randomly assigned to POAI (n=2976) or control (n=1504). On Feb 6, 2018, median follow-up was 62·9 months (IQR 58·1-74·1). 434 (10%) of 4480 women had a breast cancer recurrence (280 [9%] POAI; 154 [10%] control), hazard ratio 0·92 (95% CI 0·75-1·12); p=0·40 with the proportion free from breast cancer recurrence at 5 years of 91·0% (95% CI 89·9-92·0) for patients in the POAI group and 90·4% (88·7-91·9) in the control group. Within the POAI-treated HER2-negative subpopulation, 5-year recurrence risk in women with low Ki67 POAI has not been shown to improve treatment outcome, but can be used without detriment to help select appropriate adjuvant therapy based on tumour Ki67. Most patients with low Ki67 Cancer Research UK.

Sections du résumé

BACKGROUND
Preoperative and perioperative aromatase inhibitor (POAI) therapy has the potential to improve outcomes in women with operable oestrogen receptor-positive primary breast cancer. It has also been suggested that tumour Ki67 values after 2 weeks (Ki67
METHODS
POETIC was an open-label, multicentre, parallel-group, randomised, phase 3 trial (done in 130 UK hospitals) in which postmenopausal women aged at least 50 years with WHO performance status 0-1 and hormone receptor-positive, operable breast cancer were randomly assigned (2:1) to POAI (letrozole 2·5 mg per day orally or anastrozole 1 mg per day orally) for 14 days before and following surgery or no POAI (control). Adjuvant treatment was given as per UK standard local practice. Randomisation was done centrally by computer-generated permuted block method (variable block size of six or nine) and was stratified by hospital. Treatment allocation was not masked. The primary endpoint was time to recurrence. A key second objective explored association between Ki67 (dichotomised at 10%) and disease outcomes. The primary analysis for clinical endpoints was by modified intention to treat (excluding patients who withdrew consent). For Ki67 biomarker association and endpoint analysis, the evaluable population included all randomly assigned patients who had paired Ki67 values available. This study is registered with ClinicalTrials.gov, NCT02338310; the European Clinical Trials database, EudraCT2007-003877-21; and the ISRCTN registry, ISRCTN63882543. Recruitment is complete and long-term follow-up is ongoing.
FINDINGS
Between Oct 13, 2008, and April 16, 2014, 4480 women were recruited and randomly assigned to POAI (n=2976) or control (n=1504). On Feb 6, 2018, median follow-up was 62·9 months (IQR 58·1-74·1). 434 (10%) of 4480 women had a breast cancer recurrence (280 [9%] POAI; 154 [10%] control), hazard ratio 0·92 (95% CI 0·75-1·12); p=0·40 with the proportion free from breast cancer recurrence at 5 years of 91·0% (95% CI 89·9-92·0) for patients in the POAI group and 90·4% (88·7-91·9) in the control group. Within the POAI-treated HER2-negative subpopulation, 5-year recurrence risk in women with low Ki67
INTERPRETATION
POAI has not been shown to improve treatment outcome, but can be used without detriment to help select appropriate adjuvant therapy based on tumour Ki67. Most patients with low Ki67
FUNDING
Cancer Research UK.

Identifiants

pubmed: 33152284
pii: S1470-2045(20)30458-7
doi: 10.1016/S1470-2045(20)30458-7
pmc: PMC7606901
pii:
doi:

Substances chimiques

Aromatase Inhibitors 0
Biomarkers, Tumor 0
Estrogen Receptor alpha 0
Ki-67 Antigen 0
MKI67 protein, human 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT02338310']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1443-1454

Subventions

Organisme : Cancer Research UK
ID : 8671
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

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Auteurs

Ian Smith (I)

The Royal Marsden NHS Foundation Trust, London, UK; The Institute of Cancer Research, London, UK. Electronic address: poetic-icrctsu@icr.ac.uk.

John Robertson (J)

University of Nottingham, Nottingham, UK; University Hospitals of Derby and Burton, Derby, UK.

Lucy Kilburn (L)

The Institute of Cancer Research, London, UK.

Maggie Wilcox (M)

Independent Cancer Patients Voice, London, UK.

Abigail Evans (A)

Poole Hospital NHS Foundation Trust, Poole, UK.

Chris Holcombe (C)

Liverpool University Hospitals Foundation Trust, Liverpool, UK.

Kieran Horgan (K)

Bexley Cancer Centre, Leeds, UK.

Cliona Kirwan (C)

University of Manchester and Manchester University NHS Foundation Trust, Manchester, UK.

Elizabeth Mallon (E)

Queen Elizabeth University Hospital Glasgow, Govan, UK.

Mark Sibbering (M)

University Hospitals of Derby and Burton, Derby, UK.

Anthony Skene (A)

Royal Bournemouth and Christchurch NHS Foundation Trust, Bournemouth, UK.

Raghavan Vidya (R)

University of Birmingham and Royal Wolverhampton NHS Trust, Wolverhampton, UK.

Maggie Cheang (M)

The Institute of Cancer Research, London, UK.

Jane Banerji (J)

The Institute of Cancer Research, London, UK.

James Morden (J)

The Institute of Cancer Research, London, UK.

Kally Sidhu (K)

The Royal Marsden NHS Foundation Trust, London, UK.

Andrew Dodson (A)

The Royal Marsden NHS Foundation Trust, London, UK.

Judith M Bliss (JM)

The Institute of Cancer Research, London, UK.

Mitch Dowsett (M)

The Royal Marsden NHS Foundation Trust, London, UK; The Institute of Cancer Research, London, UK.

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Classifications MeSH