Stereotactic ablative body radiotherapy (SABR) for bone only oligometastatic breast cancer: A prospective clinical trial.


Journal

Breast (Edinburgh, Scotland)
ISSN: 1532-3080
Titre abrégé: Breast
Pays: Netherlands
ID NLM: 9213011

Informations de publication

Date de publication:
Feb 2020
Historique:
received: 23 05 2019
revised: 24 10 2019
accepted: 28 10 2019
pubmed: 18 11 2019
medline: 20 11 2020
entrez: 18 11 2019
Statut: ppublish

Résumé

Stereotactic ablative body radiotherapy (SABR) is an emerging noninvasive approach for the treatment of oligometastases. Limited prospective evidence is available in breast cancer. To determine the safety and feasibility of single fraction SABR for patients with bone only oligometastatic breast cancer. Secondary endpoints were local and distant progression-free survival (LPFS and DPFS), toxicity and response assessment. In this single institution prospective trial we screened patients with computed tomography, bone scan, and sodium fluoride positron emission tomography. Eligible patients had one to three bone only oligometastases. All patients were treated at a dose of 20Gy in 1 fraction to each metastasis. Kaplan-Meier methods were used to determine local and distant progression free survival (LPFS and DPFS). Toxicity was graded using Common Terminology Criteria for Adverse Event version 4.0. 15 eligible patients were recruited to the study. Median follow-up time was 24 months. The treatment was feasible in 12 (80%) of patients with 3 (20%) of patients having treatment delayed by more than 3 days. 10 (67%) of patients experienced grade 1 treatment related toxicity, 4 (27%) experienced grade 2 toxicity and no patients experienced grade 3 or 4 treatment related toxicity. The two-year LPFS was 100%, DPFS was 67%. We observed that SABR is feasible, well tolerated and effective in this cohort with two thirds of patients disease-free at two years. In selected patients with bone-only oligometastatic disease, SABR could be considered a treatment option. Randomised trials are required to assess the impact of SABR on overall survival when compared to the standard of care.

Sections du résumé

BACKGROUND BACKGROUND
Stereotactic ablative body radiotherapy (SABR) is an emerging noninvasive approach for the treatment of oligometastases. Limited prospective evidence is available in breast cancer.
OBJECTIVES OBJECTIVE
To determine the safety and feasibility of single fraction SABR for patients with bone only oligometastatic breast cancer. Secondary endpoints were local and distant progression-free survival (LPFS and DPFS), toxicity and response assessment.
METHODS AND MATERIALS METHODS
In this single institution prospective trial we screened patients with computed tomography, bone scan, and sodium fluoride positron emission tomography. Eligible patients had one to three bone only oligometastases. All patients were treated at a dose of 20Gy in 1 fraction to each metastasis. Kaplan-Meier methods were used to determine local and distant progression free survival (LPFS and DPFS). Toxicity was graded using Common Terminology Criteria for Adverse Event version 4.0.
RESULTS RESULTS
15 eligible patients were recruited to the study. Median follow-up time was 24 months. The treatment was feasible in 12 (80%) of patients with 3 (20%) of patients having treatment delayed by more than 3 days. 10 (67%) of patients experienced grade 1 treatment related toxicity, 4 (27%) experienced grade 2 toxicity and no patients experienced grade 3 or 4 treatment related toxicity. The two-year LPFS was 100%, DPFS was 67%.
CONCLUSION CONCLUSIONS
We observed that SABR is feasible, well tolerated and effective in this cohort with two thirds of patients disease-free at two years. In selected patients with bone-only oligometastatic disease, SABR could be considered a treatment option. Randomised trials are required to assess the impact of SABR on overall survival when compared to the standard of care.

Identifiants

pubmed: 31734589
pii: S0960-9776(19)30590-9
doi: 10.1016/j.breast.2019.10.016
pmc: PMC7375645
pii:
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

55-62

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest I have no conflict of interest.

Références

Int J Radiat Oncol Biol Phys. 2010 Mar 1;76(3 Suppl):S3-9
pubmed: 20171515
Radiother Oncol. 2018 Jan;126(1):177-180
pubmed: 28943046
N Engl J Med. 2018 Aug 02;379(5):417-427
pubmed: 29860937
AJR Am J Roentgenol. 2014 Aug;203(2):263-71
pubmed: 25055258
N Engl J Med. 2012 Mar 8;366(10):883-892
pubmed: 22397650
J Clin Oncol. 1995 Jan;13(1):8-10
pubmed: 7799047
Br J Cancer. 1998;77(2):336-40
pubmed: 9461007
Breast. 2016 Apr;26:11-7
pubmed: 27017237
PLoS Med. 2016 Dec 27;13(12):e1002204
pubmed: 28027312
Cancer. 2008 Feb 1;112(3):650-8
pubmed: 18072260
Cancer. 2007 Oct 15;110(8):1796-802
pubmed: 17786939
N Engl J Med. 2015 Jul 16;373(3):209-19
pubmed: 26030518
Ann Oncol. 2018 Jul 1;29(7):1541-1547
pubmed: 29718092
Cell. 2012 May 25;149(5):994-1007
pubmed: 22608083
Strahlenther Onkol. 1995 May;171(5):290-5
pubmed: 7770785
Eur J Cancer. 2011 Oct;47(15):2282-90
pubmed: 21741832
Int J Radiat Oncol Biol Phys. 1992;23(5):969-75
pubmed: 1322389
J Clin Oncol. 2004 Jul 15;22(14):2942-53
pubmed: 15254062
Cochrane Database Syst Rev. 2018 Mar 15;3:CD011276
pubmed: 29542106
Int J Radiat Oncol Biol Phys. 2015 Nov 15;93(4):757-64
pubmed: 26530743
J Nucl Med. 2009 May;50 Suppl 1:122S-50S
pubmed: 19403881
JAMA Oncol. 2018 Oct 1;4(10):1367-1374
pubmed: 29862411
Nature. 2015 Feb 12;518(7538):240-4
pubmed: 25409150
Cancer. 2004 Jan 1;100(1):28-35
pubmed: 14692021
Breast Cancer Res Treat. 2009 Jun;115(3):601-8
pubmed: 18719992
Cancer. 2005 Nov 15;104(10):2244-54
pubmed: 16216003
N Engl J Med. 2016 Nov 17;375(20):1925-1936
pubmed: 27959613
Lancet. 2019 May 18;393(10185):2051-2058
pubmed: 30982687
Med Phys. 2010 Aug;37(8):4078-101
pubmed: 20879569
Eur Urol. 2018 Oct;74(4):455-462
pubmed: 30227924
N Engl J Med. 2012 Feb 9;366(6):520-9
pubmed: 22149876
Ann Thorac Surg. 2013 Apr;95(4):1170-80
pubmed: 23391172
Cancer. 1988 Oct 1;62(7):1397-401
pubmed: 3416279
Cancer. 1992 Jul 1;70(1):129-35
pubmed: 1606535
J Natl Cancer Inst. 2010 Apr 7;102(7):456-63
pubmed: 20220104
Ann Thorac Surg. 1994 Dec;58(6):1599-602
pubmed: 7979721
Clin Lung Cancer. 2018 Mar;19(2):e235-e240
pubmed: 29153897
Breast Cancer Res Treat. 2008 Aug;110(3):485-91
pubmed: 17899365

Auteurs

Steven David (S)

Peter MacCallum Cancer Centre, Australia. Electronic address: steven.david@petermac.org.

Jennifer Tan (J)

Peter MacCallum Cancer Centre, Australia.

Peter Savas (P)

Peter MacCallum Cancer Centre, Australia.

Mathias Bressel (M)

Peter MacCallum Cancer Centre, Australia.

Dianne Kelly (D)

Peter MacCallum Cancer Centre, Australia.

Farshad Foroudi (F)

Olivia Newton John Cancer Centre, Australia.

Sherene Loi (S)

Peter MacCallum Cancer Centre, Australia.

Shankar Siva (S)

Peter MacCallum Cancer Centre, Australia.

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Classifications MeSH