The University of Southampton
University of Southampton Institutional Repository

Evaluating atezolizumab in patients with urinary tract squamous cell carcinoma (AURORA): study protocol for a single arm, open-label, multicentre, phase II clinical trial

Evaluating atezolizumab in patients with urinary tract squamous cell carcinoma (AURORA): study protocol for a single arm, open-label, multicentre, phase II clinical trial
Evaluating atezolizumab in patients with urinary tract squamous cell carcinoma (AURORA): study protocol for a single arm, open-label, multicentre, phase II clinical trial

Background: bladder and urinary tract cancers account for approximately 21,000 new diagnoses and 5,000 deaths annually in the UK. Approximately 90% are transitional cell carcinomas where advanced disease is treated with platinum based chemotherapy and PD-1/PD-L1 directed immunotherapy. Urinary tract squamous cell carcinoma (UTSCC) accounts for about 5% of urinary tract cancers overall making this a rare disease. We have yet to establish definitive systemic treatment options for advanced UTSCC. Preliminary translational data, from UTSCC patient tumour samples, indicate high PD-L1 expression and tumour infiltrating lymphocytes in a proportion of cases. Both of these features are associated with differential gene expression consistent with a tumour/immune microenvironment predicted to be susceptible to immune checkpoint directed immunotherapy which we will evaluate in the AURORA trial.

Methods: AURORA is a single arm, open-label, multicentre,UK phase II clinical trial. 33 patients will be recruited from UK secondary care sites. Patients with UTSCC, suitable for treatment with palliative intent, will receive atezolizumab PD-L1 directed immunotherapy (IV infusion, 1680 mg, every 28 days) for one year if tolerated. Response assessment, by cross sectional imaging will occur every 12 weeks. AURORA uses a Simon's 2-stage optimal design with best overall objective response rate (ORR, by RECIST v1.1) at a minimum of 12 weeks from commencing treatment as the primary endpoint. Secondary endpoints will include overall survival, progression-free survival, duration of response, magnitude of response using waterfall plots of target lesion measurements, quality of life using the EORTC QLQ-C30 tool, safety and tolerability (CTCAE v5) and evaluation of potential biomarkers of treatment response including PD-L1 expression. Archival tumour samples and blood samples will be collected for translational analyses.

Discussion: if this trial shows atezolizumab to be safe and effective it may lead to a future late phase randomised controlled trial in UTSCC. Ultimately, we hope to provide a new option for treatment for such patients.

Trial registrations: EudraCT Number: 2021-001995-32 (issued 8th September 2021); ISRCTN83474167 (registered 11 May 2022); NCT05038657 (issued 9th September 2021).

B7-H1 Antigen, Carcinoma, Squamous Cell/drug therapy, Clinical Trials, Phase II as Topic, Humans, Multicenter Studies as Topic, Quality of Life, Randomized Controlled Trials as Topic, Tumor Microenvironment, Urinary Tract, PD-L1 expression, Phase II, Translational research, Immunotherapy, Urinary tract squamous cell carcinoma, Atezolizumab
1471-2407
Crabb, Simon
bcd1b566-7677-4f81-8429-3ab0e85f8373
Wickens, Robin
b734aa86-eb28-4683-a4b2-2e37053d27e4
Jane-Bibby, Sarah
caf1a038-7ce0-46b1-a163-6f71f2b8905f
Dunkley, Denise
e98e58b2-c313-4aa4-8855-43887efe49b5
Lawrence, Megan
e217da1e-b347-4129-b22f-0c8bae5eaf78
Knight, Allen
f5fb0616-dbf5-4524-86a7-8f810f8ec557
Jones, Robert
e8f24a54-68be-462f-b7ee-afb7d3438ba3
Birtle, Alison
1031c636-ab1a-4bc5-b053-5f1334c6c087
Huddart, Robert
9b98e268-407a-4dc5-85de-884cadb943a7
Linch, Mark
c677c64a-517b-4055-9041-085a4db008a0
Martin, Jonathan
10ae86a0-d3d0-463d-9d2f-58c07a3b0c0c
Coleman, Adam
49cf504d-6f2b-422b-9c3a-17eb5d5d6a85
Boukas, Konstantinos
4cbff114-7077-45ad-95e7-2c6a03761380
Markham, Hannah
ec17dffc-bef4-4397-9c5f-dc4445c1ea98
Griffiths, Gareth
7fd300c0-d279-4ff6-842d-aa1f2b9b864d
Crabb, Simon
bcd1b566-7677-4f81-8429-3ab0e85f8373
Wickens, Robin
b734aa86-eb28-4683-a4b2-2e37053d27e4
Jane-Bibby, Sarah
caf1a038-7ce0-46b1-a163-6f71f2b8905f
Dunkley, Denise
e98e58b2-c313-4aa4-8855-43887efe49b5
Lawrence, Megan
e217da1e-b347-4129-b22f-0c8bae5eaf78
Knight, Allen
f5fb0616-dbf5-4524-86a7-8f810f8ec557
Jones, Robert
e8f24a54-68be-462f-b7ee-afb7d3438ba3
Birtle, Alison
1031c636-ab1a-4bc5-b053-5f1334c6c087
Huddart, Robert
9b98e268-407a-4dc5-85de-884cadb943a7
Linch, Mark
c677c64a-517b-4055-9041-085a4db008a0
Martin, Jonathan
10ae86a0-d3d0-463d-9d2f-58c07a3b0c0c
Coleman, Adam
49cf504d-6f2b-422b-9c3a-17eb5d5d6a85
Boukas, Konstantinos
4cbff114-7077-45ad-95e7-2c6a03761380
Markham, Hannah
ec17dffc-bef4-4397-9c5f-dc4445c1ea98
Griffiths, Gareth
7fd300c0-d279-4ff6-842d-aa1f2b9b864d

Crabb, Simon, Wickens, Robin, Jane-Bibby, Sarah, Dunkley, Denise, Lawrence, Megan, Knight, Allen, Jones, Robert, Birtle, Alison, Huddart, Robert, Linch, Mark, Martin, Jonathan, Coleman, Adam, Boukas, Konstantinos, Markham, Hannah and Griffiths, Gareth (2023) Evaluating atezolizumab in patients with urinary tract squamous cell carcinoma (AURORA): study protocol for a single arm, open-label, multicentre, phase II clinical trial. BMC cancer, 23 (1), [885]. (doi:10.1186/s12885-023-11397-x).

Record type: Article

Abstract

Background: bladder and urinary tract cancers account for approximately 21,000 new diagnoses and 5,000 deaths annually in the UK. Approximately 90% are transitional cell carcinomas where advanced disease is treated with platinum based chemotherapy and PD-1/PD-L1 directed immunotherapy. Urinary tract squamous cell carcinoma (UTSCC) accounts for about 5% of urinary tract cancers overall making this a rare disease. We have yet to establish definitive systemic treatment options for advanced UTSCC. Preliminary translational data, from UTSCC patient tumour samples, indicate high PD-L1 expression and tumour infiltrating lymphocytes in a proportion of cases. Both of these features are associated with differential gene expression consistent with a tumour/immune microenvironment predicted to be susceptible to immune checkpoint directed immunotherapy which we will evaluate in the AURORA trial.

Methods: AURORA is a single arm, open-label, multicentre,UK phase II clinical trial. 33 patients will be recruited from UK secondary care sites. Patients with UTSCC, suitable for treatment with palliative intent, will receive atezolizumab PD-L1 directed immunotherapy (IV infusion, 1680 mg, every 28 days) for one year if tolerated. Response assessment, by cross sectional imaging will occur every 12 weeks. AURORA uses a Simon's 2-stage optimal design with best overall objective response rate (ORR, by RECIST v1.1) at a minimum of 12 weeks from commencing treatment as the primary endpoint. Secondary endpoints will include overall survival, progression-free survival, duration of response, magnitude of response using waterfall plots of target lesion measurements, quality of life using the EORTC QLQ-C30 tool, safety and tolerability (CTCAE v5) and evaluation of potential biomarkers of treatment response including PD-L1 expression. Archival tumour samples and blood samples will be collected for translational analyses.

Discussion: if this trial shows atezolizumab to be safe and effective it may lead to a future late phase randomised controlled trial in UTSCC. Ultimately, we hope to provide a new option for treatment for such patients.

Trial registrations: EudraCT Number: 2021-001995-32 (issued 8th September 2021); ISRCTN83474167 (registered 11 May 2022); NCT05038657 (issued 9th September 2021).

Text
s12885-023-11397-x - Version of Record
Available under License Creative Commons Attribution.
Download (1MB)

More information

Accepted/In Press date: 12 September 2023
Published date: 19 September 2023
Additional Information: Funding Information: Recruitment is supported by the research nurses and staff within the NIHR Clinical Research Network in England and Wales and equivalent in Scotland. Funding Information: Recruitment is supported by the research nurses and staff within the NIHR Clinical Research Network in England and Wales and equivalent in Scotland. University Hospital Southampton NHS Foundation Trust are the sponsor for this trial (ref. RHM CAN1665; sponsor@uhs.nhs.uk). The study sponsor was not involved in the study design; writing of the protocol paper; or the decision to submit the paper for publication. Funding Information: The study is funded by Cancer Research UK (CRCPJT\100018), with free provision of atezolizumab by Roche and supported by CRUK core funding at SCTU. Publisher Copyright: © 2023, BioMed Central Ltd., part of Springer Nature.
Keywords: B7-H1 Antigen, Carcinoma, Squamous Cell/drug therapy, Clinical Trials, Phase II as Topic, Humans, Multicenter Studies as Topic, Quality of Life, Randomized Controlled Trials as Topic, Tumor Microenvironment, Urinary Tract, PD-L1 expression, Phase II, Translational research, Immunotherapy, Urinary tract squamous cell carcinoma, Atezolizumab

Identifiers

Local EPrints ID: 482831
URI: http://eprints.soton.ac.uk/id/eprint/482831
ISSN: 1471-2407
PURE UUID: 26b4880d-3e50-4bdb-b82a-022dbb9dcaa5
ORCID for Simon Crabb: ORCID iD orcid.org/0000-0003-3521-9064
ORCID for Gareth Griffiths: ORCID iD orcid.org/0000-0002-9579-8021

Catalogue record

Date deposited: 13 Oct 2023 16:31
Last modified: 18 Mar 2024 03:30

Export record

Altmetrics

Contributors

Author: Simon Crabb ORCID iD
Author: Robin Wickens
Author: Sarah Jane-Bibby
Author: Denise Dunkley
Author: Megan Lawrence
Author: Allen Knight
Author: Robert Jones
Author: Alison Birtle
Author: Robert Huddart
Author: Mark Linch
Author: Jonathan Martin
Author: Adam Coleman
Author: Konstantinos Boukas
Author: Hannah Markham

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.

×