Determining Planning Priorities for SABR for Oligometastatic Disease: A Secondary Analysis of the SABR-COMET Phase II Randomized Trial.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 12 2022
Historique:
received: 01 10 2021
revised: 29 11 2021
accepted: 03 01 2022
pubmed: 16 1 2022
medline: 22 11 2022
entrez: 15 1 2022
Statut: ppublish

Résumé

SABR may improve survival in patients with oligometastases, but for some lesions, safe delivery of SABR may require a reduction in delivered dose or target coverage. This study assessed the association between target coverage compromise and oncologic and survival outcomes. Patients with a controlled primary malignancy and 1 to 5 oligometastases were randomized (1:2) between standard of care (SOC) treatment and SOC plus SABR. In patients receiving SABR, the target dose coverage was reduced to meet organ at risk (OAR) constraints, if necessary. The D99 value (minimum dose received by the hottest 99% of the planning target volume [PTV]) was used as a measure of PTV coverage for each treatment plan, and the relationship between the coverage compromise index (CCI, defined as D99/prescription dose) and patient outcomes was assessed. Sixty-two patients in the SABR arm had dosimetric information available and a total of 109 lesions were evaluated. The mean CCI per lesion was 0.96 (95% CI, 0.56-1.61). Of the 109 lesions evaluated, 29.4% (n = 32) required coverage compromise (CCI <0.9). Adrenal metastases required coverage compromise in 100% of analyzed lesions (n = 7). CCI was not significantly associated with lesional control, adverse events, overall survival (OS), or progression-free survival (PFS). Target compromise was required in a substantial minority of cases, but PTV coverage was not associated with OS, progression-free survival, or lesional control. This suggests that OAR constraints used for SABR treatments in the oligometastatic setting should continue to be prioritized during planning.

Identifiants

pubmed: 35031340
pii: S0360-3016(22)00005-0
doi: 10.1016/j.ijrobp.2022.01.002
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1016-1021

Informations de copyright

Copyright © 2022 Elsevier Inc. All rights reserved.

Auteurs

Matthew Van Oirschot (M)

London Health Sciences Centre, London, Ontario, Canada.

Alanah Bergman (A)

British Columbia Cancer, Vancouver Centre, Vancouver, British Columbia, Canada.

Wilko F A R Verbakel (WFAR)

Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Lucy Ward (L)

Nova Scotia Health, Halifax, Nova Scotia, Canada.

Isabelle Gagne (I)

British Columbia Cancer, Victoria Centre, Victoria, British Columbia, Canada.

Vicky Huang (V)

British Columbia Cancer, Surrey Centre, Surrey, British Columbia, Canada.

Nick Chng (N)

British Columbia Cancer, Centre for the North, Prince George, British Columbia, Canada.

Peter Houston (P)

Beatson West of Scotland Cancer Centre, Glasgow, Scotland.

Kerry Symes (K)

British Columbia Cancer, Vancouver Centre, Vancouver, British Columbia, Canada.

Christopher G Thomas (CG)

Nova Scotia Health, Halifax, Nova Scotia, Canada.

Parminder Basran (P)

Cornell University, Ithaca, New York.

David Bowes (D)

Nova Scotia Health, Halifax, Nova Scotia, Canada.

Stephen Harrow (S)

Beatson West of Scotland Cancer Centre, Glasgow, Scotland.

Robert Olson (R)

British Columbia Cancer, Centre for the North, Prince George, British Columbia, Canada.

Suresh Senan (S)

Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Andrew Warner (A)

London Health Sciences Centre, London, Ontario, Canada.

David A Palma (DA)

London Health Sciences Centre, London, Ontario, Canada.

Stewart Gaede (S)

London Health Sciences Centre, London, Ontario, Canada. Electronic address: Stewart.Gaede@LHSC.on.ca.

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Classifications MeSH