Bridging the age gap in breast cancer. Impacts of omission of breast cancer surgery in older women with oestrogen receptor positive early breast cancer. A risk stratified analysis of survival outcomes and quality of life.

Adjuvant endocrine therapy Breast cancer Older women Patient-centred outcomes Primary endocrine therapy Propensity score matching Quality of life Surgery Survival

Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
01 2021
Historique:
received: 18 06 2020
revised: 14 09 2020
accepted: 06 10 2020
pubmed: 22 11 2020
medline: 24 4 2021
entrez: 21 11 2020
Statut: ppublish

Résumé

Age-related breast cancer treatment variance is widespread with many older women having primary endocrine therapy (PET), which may contribute to inferior survival and local control. This propensity-matched study determined if a subgroup of older women may safely be offered PET. Multicentre, prospective, UK, observational cohort study with propensity-matched analysis to determine optimal allocation of surgery plus ET (S+ET) or PET in women aged ≥70 with breast cancer. Data on fitness, frailty, cancer stage, grade, biotype, treatment and quality of life were collected. Propensity-matching (based on age, health status and cancer stage) adjusted for allocation bias when comparing S+ET with PET. A total of 3416 women (median age 77, range 69-102) were recruited from 56 breast units-2854 (88%) had ER+ breast cancer: 2354 had S+ET and 500 PET. Median follow-up was 52 months. Patients treated with PET were older and frailer than patients treated with S+ET. Unmatched overall survival was inferior in the PET group (hazard ratio, (HR) 0.27, 95% confidence interval (CI) 0.23-0.33, P < 0.001). Unmatched breast cancer-specific survival (BCSS) was also inferior in patients treated with PET (HR: 0.41, CI: 0.29-0.58, P < 0.001 for BCSS). In the matched analysis, PET was still associated with an inferior overall survival (HR = 0.72, 95% CI: 0.53-0.98, P = 0.04) but not BCSS (HR = 0.74, 95% CI: 0.40-1.37, P = 0.34) although at 4-5 years subtle divergence of the curves commenced in favor of surgery. Global health status diverged at certain time points between groups but over 24 months was similar when adjusted for baseline variance. For the majority of older women with early ER+ breast cancer, surgery is oncologically superior to PET. In less fit, older women, with characteristics similar to the matched cohort of this study (median age 81 with higher comorbidity and functional impairment burdens, the BCSS survival differential disappears at least out to 4-5 year follow-up, suggesting that for those with less than 5-year predicted life-expectancy (>90 years or >85 with comorbidities or frailty) individualised decision making regarding PET versus S+ET may be appropriate and safe to offer. The Age Gap online decision tool may support this decision-making process (https://agegap.shef.ac.uk/). ISRCTN: 46099296.

Sections du résumé

BACKGROUND
Age-related breast cancer treatment variance is widespread with many older women having primary endocrine therapy (PET), which may contribute to inferior survival and local control. This propensity-matched study determined if a subgroup of older women may safely be offered PET.
METHODS
Multicentre, prospective, UK, observational cohort study with propensity-matched analysis to determine optimal allocation of surgery plus ET (S+ET) or PET in women aged ≥70 with breast cancer. Data on fitness, frailty, cancer stage, grade, biotype, treatment and quality of life were collected. Propensity-matching (based on age, health status and cancer stage) adjusted for allocation bias when comparing S+ET with PET.
FINDINGS
A total of 3416 women (median age 77, range 69-102) were recruited from 56 breast units-2854 (88%) had ER+ breast cancer: 2354 had S+ET and 500 PET. Median follow-up was 52 months. Patients treated with PET were older and frailer than patients treated with S+ET. Unmatched overall survival was inferior in the PET group (hazard ratio, (HR) 0.27, 95% confidence interval (CI) 0.23-0.33, P < 0.001). Unmatched breast cancer-specific survival (BCSS) was also inferior in patients treated with PET (HR: 0.41, CI: 0.29-0.58, P < 0.001 for BCSS). In the matched analysis, PET was still associated with an inferior overall survival (HR = 0.72, 95% CI: 0.53-0.98, P = 0.04) but not BCSS (HR = 0.74, 95% CI: 0.40-1.37, P = 0.34) although at 4-5 years subtle divergence of the curves commenced in favor of surgery. Global health status diverged at certain time points between groups but over 24 months was similar when adjusted for baseline variance.
INTERPRETATION
For the majority of older women with early ER+ breast cancer, surgery is oncologically superior to PET. In less fit, older women, with characteristics similar to the matched cohort of this study (median age 81 with higher comorbidity and functional impairment burdens, the BCSS survival differential disappears at least out to 4-5 year follow-up, suggesting that for those with less than 5-year predicted life-expectancy (>90 years or >85 with comorbidities or frailty) individualised decision making regarding PET versus S+ET may be appropriate and safe to offer. The Age Gap online decision tool may support this decision-making process (https://agegap.shef.ac.uk/).
TRIAL REGISTRATION NUMBER
ISRCTN: 46099296.

Identifiants

pubmed: 33220653
pii: S0959-8049(20)31274-0
doi: 10.1016/j.ejca.2020.10.015
pmc: PMC7789991
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

48-62

Subventions

Organisme : Department of Health
ID : RP-PG-1209-10071
Pays : United Kingdom

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest statement None declared.

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Auteurs

Lynda Wyld (L)

Department of Oncology and Metabolism, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK. Electronic address: l.wyld@sheffield.ac.uk.

Malcolm W R Reed (MWR)

Brighton and Sussex Medical School, Falmer, Brighton, UK.

Jenna Morgan (J)

Department of Oncology and Metabolism, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK.

Karen Collins (K)

College of Health, Wellbeing and Life Sciences, Department of Allied Health Professions, Sheffield Hallam University, Collegiate Cresent Campus, Sheffield, UK.

Sue Ward (S)

Department of Health Economics and Decision Science, School for Health and Related Research, ScHARR, University of Sheffield, UK.

Geoffrey R Holmes (GR)

Department of Health Economics and Decision Science, School for Health and Related Research, ScHARR, University of Sheffield, UK.

Mike Bradburn (M)

Clinical Trials Research Unit, School for Health and Related Research, University of Sheffield, UK.

Stephen Walters (S)

Clinical Trials Research Unit, School for Health and Related Research, University of Sheffield, UK.

Maria Burton (M)

College of Health, Wellbeing and Life Sciences, Department of Allied Health Professions, Sheffield Hallam University, Collegiate Cresent Campus, Sheffield, UK.

Esther Herbert (E)

Clinical Trials Research Unit, School for Health and Related Research, University of Sheffield, UK.

Kate Lifford (K)

Division of Population Medicine, Cardiff University, 8th Floor, Neuadd Meirionnydd, Heath Park, Cardiff, CF14 4YS, UK.

Adrian Edwards (A)

Division of Population Medicine, Cardiff University, 8th Floor, Neuadd Meirionnydd, Heath Park, Cardiff, CF14 4YS, UK.

Alistair Ring (A)

The Royal Marsden Hospital NHS Foundation Trust, London, UK.

Thompson Robinson (T)

Department of Cardiovascular Sciences and NIHR Biomedical Research Centre, University of Leicester, Cardiovascular Research Centre, The Glenfield General Hospital, Leicester, LE3 9QP, UK.

Charlene Martin (C)

Department of Oncology and Metabolism, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK.

Tim Chater (T)

Clinical Trials Research Unit, School for Health and Related Research, University of Sheffield, UK.

Kirsty Pemberton (K)

Clinical Trials Research Unit, School for Health and Related Research, University of Sheffield, UK.

Anne Shrestha (A)

Department of Oncology and Metabolism, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK.

Alan Brennan (A)

Department of Health Economics and Decision Science, School for Health and Related Research, ScHARR, University of Sheffield, UK.

Kwok L Cheung (KL)

University of Nottingham, Royal Derby Hospital, Uttoxeter Road, Derby, DE22 3DT, UK.

Annaliza Todd (A)

Department of Oncology and Metabolism, University of Sheffield Medical School, Beech Hill Road, Sheffield, S10 2RX, UK.

Riccardo Audisio (R)

University of Gothenberg, Sahlgrenska Universitetssjukhuset, 41345 Göteborg, Sweden.

Juliet Wright (J)

Brighton and Sussex Medical School, Falmer, Brighton, UK.

Richard Simcock (R)

Brighton and Sussex Medical School, Falmer, Brighton, UK.

Tracy Green (T)

Yorkshire and Humber Consumer Research Panel, UK.

Deirdre Revell (D)

Yorkshire and Humber Consumer Research Panel, UK.

Jacqui Gath (J)

Yorkshire and Humber Consumer Research Panel, UK.

Kieran Horgan (K)

Dept of Breast Surgery, Bexley Cancer Centre, St James's University Hospital, Leeds, LS9 7TF, UK.

Chris Holcombe (C)

Liverpool University Hospitals Foundation Trust, Prescott Street, Liverpool L7 8 XP, UK.

Matt Winter (M)

Weston Park Hospital, Whitham Rd, Sheffield S10 2SJ, UK.

Jay Naik (J)

Pinderfields Hospital, Mid Yorkshire NHS Foundation Trust, Aberford Rd, Wakefield, UK.

Rishi Parmeshwar (R)

University Hospitals of Morecambe Bay, Royal Lancashire Infirmary Ashton Road, Lancaster, Lancashire, LA1 4RP, UK.

Julietta Patnick (J)

Cancer Epidemiology Unit, Nuffield Department of Population Health, University of Oxford, UK.

Margot Gosney (M)

Royal Berkshire NHS Foundation Trust, Reading, RG1 5AN, UK.

Matthew Hatton (M)

Weston Park Hospital, Whitham Rd, Sheffield S10 2SJ, UK.

Alastair M Thomson (AM)

Department of Surgery, Baylor College of Medicine, One Baylor Plaza, Houston, TX, USA.

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Classifications MeSH