Is SABR Cost-Effective in Oligometastatic Cancer? An Economic Analysis of the SABR-COMET 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 04 2021
Historique:
received: 09 09 2020
revised: 25 10 2020
accepted: 01 12 2020
pubmed: 15 12 2020
medline: 31 7 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

The phase 2 randomized study SABR-COMET demonstrated that in patients with controlled primary tumors and 1 to 5 oligometastatic lesions, SABR was associated with improved progression-free survival (PFS) compared with standard of care (SoC), but with higher costs and treatment-related toxicities. The aim of this study was to assess the cost-effectiveness of SABR versus SoC in this setting. A Markov model was constructed to perform a cost-utility analysis from the Canadian health care system perspective. Utility values and transition probabilities were derived from individual-level data from the SABR-COMET trial. One-way, 2-way, and probabilistic sensitivity analyses were performed. Costs were expressed in 2018 CAD. A separate analysis based on US payer's perspective was performed. An incremental cost-effectiveness ratio (ICER) at a willingness-to-pay threshold of $100,000 per quality-adjusted life year (QALY) was used. In the base case scenario, SABR was cost-effective at an ICER of $37,157 per QALY gained. This finding was most sensitive to the number of metastatic lesions treated with SABR (ICER: $28,066 per QALY for 2, increasing to $64,429 per QALY for 5), difference in chemotherapy use (ICER: $27,173-$53,738 per QALY), and PFS hazard ratio (HR) between strategies (ICER: $31,548-$53,273 per QALY). Probabilistic sensitivity analysis revealed that SABR was cost-effective in 97% of all iterations. Two-way sensitivity analysis demonstrated a nonlinear relationship between the number of lesions and the PFS HR. To maintain cost-effectiveness for each additional metastasis, the HR must decrease by approximately 0.047. The US cost analysis yielded similar results, with an ICER of $54,564 (2018 USD per QALY) for SABR. SABR is cost-effective for patients with 1 to 5 oligometastatic lesions compared with SoC.

Identifiants

pubmed: 33309977
pii: S0360-3016(20)34645-9
doi: 10.1016/j.ijrobp.2020.12.001
pii:
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1176-1184

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

X Melody Qu (XM)

London Health Sciences Centre, London, Canada; Schulich School of Medicine & Dentistry, Western University, London, Canada.

Yujie Chen (Y)

Schulich School of Medicine & Dentistry, Western University, London, Canada.

Gregory S Zaric (GS)

Schulich School of Medicine & Dentistry, Western University, London, Canada; Ivey Business School, Western University, London, Canada.

Suresh Senan (S)

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

Robert A Olson (RA)

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

Stephen Harrow (S)

Beatson West of Scotland Cancer Centre, Glasgow, Scotland.

Ava John-Baptiste (A)

London Health Sciences Centre, London, Canada; Schulich School of Medicine & Dentistry, Western University, London, Canada.

Stewart Gaede (S)

London Health Sciences Centre, London, Canada.

Liam A Mulroy (LA)

Nova Scotia Cancer Centre, Halifax, Canada.

Devin Schellenberg (D)

British Columbia Cancer, Surrey Centre, Surrey, Canada.

Sashendra Senthi (S)

Alfred Health Radiation Oncology, Melbourne, Australia.

Anand Swaminath (A)

Juravinski Cancer Centre, Hamilton, Canada.

Neil Kopek (N)

McGill University Health Centre, Montreal, Canada.

Mitchell Liu (M)

British Columbia Cancer, Vancouver Centre, Vancouver, Canada.

Andrew Warner (A)

London Health Sciences Centre, London, Canada.

George B Rodrigues (GB)

London Health Sciences Centre, London, Canada; Schulich School of Medicine & Dentistry, Western University, London, Canada.

David A Palma (DA)

London Health Sciences Centre, London, Canada; Schulich School of Medicine & Dentistry, Western University, London, Canada.

Alexander V Louie (AV)

London Health Sciences Centre, London, Canada; Schulich School of Medicine & Dentistry, Western University, London, Canada; Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Canada. Electronic address: alexander.louie@sunnybrook.ca.

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Classifications MeSH