The University of Southampton
University of Southampton Institutional Repository

Olaratumab in combination with Doxorubicin for the treatment of advanced soft tissue sarcoma: an Evidence Review Group perspective of a National Institute for Health and Care Excellence single technology appraisal

Olaratumab in combination with Doxorubicin for the treatment of advanced soft tissue sarcoma: an Evidence Review Group perspective of a National Institute for Health and Care Excellence single technology appraisal
Olaratumab in combination with Doxorubicin for the treatment of advanced soft tissue sarcoma: an Evidence Review Group perspective of a National Institute for Health and Care Excellence single technology appraisal

The manufacturer of olaratumab (Lartruvo®), Eli Lilly & Company Limited, submitted evidence for the clinical and cost effectiveness of this drug, in combination with doxorubicin, for untreated advanced soft tissue sarcoma (STS) not amenable to surgery or radiotherapy, as part of the National Institute for Health and Care Excellence (NICE) Single Technology Appraisal process. The Peninsula Technology Assessment Group, commissioned to act as the Evidence Review Group (ERG), critically reviewed the company’s submission. Clinical effectiveness evidence for the company’s analysis was derived from an open-label, randomised controlled trial, JGDG. The analysis was based on a partitioned survival model with a time horizon of 25 years, and the perspective was of the UK National Health Service (NHS) and Personal Social Services. Costs and benefits were discounted at 3.5% per year. Given the available evidence, olaratumab is likely to meet NICE’s end-of-life criteria. To improve the cost effectiveness of olaratumab, the company offered a discount through a Commercial Access Agreement (CAA) with the NHS England. When the discount was applied, the mean base-case and probabilistic incremental cost-effectiveness ratios (ICERs) for olaratumab plus doxorubicin versus the standard-of-care doxorubicin were £46,076 and £47,127 per quality-adjusted life-year (QALY) gained, respectively; the probability of this treatment being cost effective at the willingness-to-pay threshold of £50,000 per QALY gained, applicable to end-of-life treatments, was 0.54. The respective ICERs from the ERG’s analysis were approximately £60,000/QALY gained, and the probability of the treatment being cost effective was 0.21. In August 2017, the NICE Appraisal Committee recommended olaratumab in combination with doxorubicin for this indication for use via the UK Cancer Drugs Fund under the agreed CAA until further evidence being collected in the ongoing phase III trial—ANNOUNCE—becomes available in December 2020.

1170-7690
39-49
Tikhonova, Irina A.
577ccbcc-6643-4190-bb6d-19e13b44bcd1
Jones-Hughes, Tracey
6350a7df-c6eb-4729-9156-f67c4992886c
Dunham, James
bfbcbb61-3d53-4a22-80b4-ce336c84c386
Warren, Fiona C.
bab70ba8-cbd5-4419-a9b2-9b0d716d068e
Robinson, Sophie
ca6f6393-f165-4a34-98a5-d90541c7b851
Stephens, Peter
1303602d-0f0a-47f9-8daa-1e4af59bf9de
Hoyle, Martin
c45bff8b-b34d-4622-a09a-61d4af518969
Tikhonova, Irina A.
577ccbcc-6643-4190-bb6d-19e13b44bcd1
Jones-Hughes, Tracey
6350a7df-c6eb-4729-9156-f67c4992886c
Dunham, James
bfbcbb61-3d53-4a22-80b4-ce336c84c386
Warren, Fiona C.
bab70ba8-cbd5-4419-a9b2-9b0d716d068e
Robinson, Sophie
ca6f6393-f165-4a34-98a5-d90541c7b851
Stephens, Peter
1303602d-0f0a-47f9-8daa-1e4af59bf9de
Hoyle, Martin
c45bff8b-b34d-4622-a09a-61d4af518969

Tikhonova, Irina A., Jones-Hughes, Tracey, Dunham, James, Warren, Fiona C., Robinson, Sophie, Stephens, Peter and Hoyle, Martin (2018) Olaratumab in combination with Doxorubicin for the treatment of advanced soft tissue sarcoma: an Evidence Review Group perspective of a National Institute for Health and Care Excellence single technology appraisal. PharmacoEconomics, 36 (1), 39-49. (doi:10.1007/s40273-017-0568-3).

Record type: Review

Abstract

The manufacturer of olaratumab (Lartruvo®), Eli Lilly & Company Limited, submitted evidence for the clinical and cost effectiveness of this drug, in combination with doxorubicin, for untreated advanced soft tissue sarcoma (STS) not amenable to surgery or radiotherapy, as part of the National Institute for Health and Care Excellence (NICE) Single Technology Appraisal process. The Peninsula Technology Assessment Group, commissioned to act as the Evidence Review Group (ERG), critically reviewed the company’s submission. Clinical effectiveness evidence for the company’s analysis was derived from an open-label, randomised controlled trial, JGDG. The analysis was based on a partitioned survival model with a time horizon of 25 years, and the perspective was of the UK National Health Service (NHS) and Personal Social Services. Costs and benefits were discounted at 3.5% per year. Given the available evidence, olaratumab is likely to meet NICE’s end-of-life criteria. To improve the cost effectiveness of olaratumab, the company offered a discount through a Commercial Access Agreement (CAA) with the NHS England. When the discount was applied, the mean base-case and probabilistic incremental cost-effectiveness ratios (ICERs) for olaratumab plus doxorubicin versus the standard-of-care doxorubicin were £46,076 and £47,127 per quality-adjusted life-year (QALY) gained, respectively; the probability of this treatment being cost effective at the willingness-to-pay threshold of £50,000 per QALY gained, applicable to end-of-life treatments, was 0.54. The respective ICERs from the ERG’s analysis were approximately £60,000/QALY gained, and the probability of the treatment being cost effective was 0.21. In August 2017, the NICE Appraisal Committee recommended olaratumab in combination with doxorubicin for this indication for use via the UK Cancer Drugs Fund under the agreed CAA until further evidence being collected in the ongoing phase III trial—ANNOUNCE—becomes available in December 2020.

This record has no associated files available for download.

More information

e-pub ahead of print date: 15 September 2017
Published date: January 2018

Identifiers

Local EPrints ID: 438190
URI: http://eprints.soton.ac.uk/id/eprint/438190
ISSN: 1170-7690
PURE UUID: b246519e-a896-46fe-8ec7-a241d5829665
ORCID for Irina A. Tikhonova: ORCID iD orcid.org/0000-0003-2723-0802

Catalogue record

Date deposited: 04 Mar 2020 17:30
Last modified: 17 Mar 2024 12:37

Export record

Altmetrics

Contributors

Author: Irina A. Tikhonova ORCID iD
Author: Tracey Jones-Hughes
Author: James Dunham
Author: Fiona C. Warren
Author: Sophie Robinson
Author: Peter Stephens
Author: Martin Hoyle

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×