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ELEVATE - evaluating Temozolomide and Nivolumab in patients with advanced unresectable previously treated oesophagogastric adenocarcinoma with MGMT methylation: study protocol for a single arm phase II trial

ELEVATE - evaluating Temozolomide and Nivolumab in patients with advanced unresectable previously treated oesophagogastric adenocarcinoma with MGMT methylation: study protocol for a single arm phase II trial
ELEVATE - evaluating Temozolomide and Nivolumab in patients with advanced unresectable previously treated oesophagogastric adenocarcinoma with MGMT methylation: study protocol for a single arm phase II trial

BACKGROUND: For patients with oesophagogastric adenocarcinoma, surgery is the only curative option and despite the use of multimodality therapy, which combines it with chemotherapy and/or radiotherapy, more than 50% of patients will relapse and die. Many UK patients present with advanced disease which is already inoperable or metastatic at diagnosis. For these patients, standard care chemotherapy only offers them survival of less than a year. Nivolumab, a checkpoint blockade inhibitor, has been found to work in some advanced cancers. It is proposed, for those where immunotherapy hasn't worked, that these immunologically evasive tumours need to be sensitized to immunotherapy drugs to allow them to act.

METHODS: ELEVATE is a single arm phase II trial testing the overall response to nivolumab following temozolomide treatment in patients with advanced unresectable previously treated adenocarcinoma which is O6-methylguanine-DNA-methyltransferase (MGMT) methylated. 18 patients are being recruited from UK secondary care sites. To be eligible, participants must have been treated with at least 3 months of platinum and fluoropyrimidine chemotherapy. Participants will receive 50 mg/m2 temozolomide continuously for 3 months. If their disease progresses during the 3 months, they will stop temozolomide and start nivolumab at a dose of 240mg every 2 weeks. If there is no progression after 3 months the participant will continue taking temozolomide in combination with nivolumab. All treatment will stop once the participant progresses on nivolumab. The primary endpoint is the best overall response to nivolumab, using both Response Evaluation Criteria in Solid Tumours version 1.1 and immunotherapy modified Response Evaluation Criteria in Solid Tumours. Secondary endpoints include progression-free survival, overall survival, and quality of life.

DISCUSSION: ELEVATE will provide evidence for whether giving nivolumab after temozolomide in patients with previously treated advanced oesophagogastric adenocarcinoma is safe and biologically effective prior to future randomised trials.

TRIAL REGISTRATIONS: EudraCT Number: 2020-004771-41 (issued 01 October 2020); ISCRTN11398887 (registered 14 July 2021).

Immunotherapy, MGMT methylated, Oesophagogastric adenocarcinoma, Phase II
1471-2407
946
Smyth, Elizabeth
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Cozens, Kelly
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Griffiths, Daniel
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Clark, Kathryn L
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Ewings, Sean
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Petty, Russell
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Underwood, Tim
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Fitzgerald, Rebecca C
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Tanner, James
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Giger, Olivier
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Anand, Shubha
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Griffiths, Gareth
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Smyth, Elizabeth
73725205-a097-431d-867e-e20c7869e4c4
Cozens, Kelly
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Griffiths, Daniel
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Clark, Kathryn L
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Ewings, Sean
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Petty, Russell
b939c114-e5f3-4d46-ad6e-b31c2cfcc704
Underwood, Tim
8e81bf60-edd2-4b0e-8324-3068c95ea1c6
Fitzgerald, Rebecca C
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Tanner, James
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Giger, Olivier
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Anand, Shubha
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Griffiths, Gareth
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Smyth, Elizabeth, Cozens, Kelly, Griffiths, Daniel, Clark, Kathryn L, Ewings, Sean, Petty, Russell, Underwood, Tim, Fitzgerald, Rebecca C, Tanner, James, Giger, Olivier, Anand, Shubha and Griffiths, Gareth (2022) ELEVATE - evaluating Temozolomide and Nivolumab in patients with advanced unresectable previously treated oesophagogastric adenocarcinoma with MGMT methylation: study protocol for a single arm phase II trial. BMC cancer, 22 (1), 946, [946]. (doi:10.1186/s12885-022-09891-9).

Record type: Article

Abstract

BACKGROUND: For patients with oesophagogastric adenocarcinoma, surgery is the only curative option and despite the use of multimodality therapy, which combines it with chemotherapy and/or radiotherapy, more than 50% of patients will relapse and die. Many UK patients present with advanced disease which is already inoperable or metastatic at diagnosis. For these patients, standard care chemotherapy only offers them survival of less than a year. Nivolumab, a checkpoint blockade inhibitor, has been found to work in some advanced cancers. It is proposed, for those where immunotherapy hasn't worked, that these immunologically evasive tumours need to be sensitized to immunotherapy drugs to allow them to act.

METHODS: ELEVATE is a single arm phase II trial testing the overall response to nivolumab following temozolomide treatment in patients with advanced unresectable previously treated adenocarcinoma which is O6-methylguanine-DNA-methyltransferase (MGMT) methylated. 18 patients are being recruited from UK secondary care sites. To be eligible, participants must have been treated with at least 3 months of platinum and fluoropyrimidine chemotherapy. Participants will receive 50 mg/m2 temozolomide continuously for 3 months. If their disease progresses during the 3 months, they will stop temozolomide and start nivolumab at a dose of 240mg every 2 weeks. If there is no progression after 3 months the participant will continue taking temozolomide in combination with nivolumab. All treatment will stop once the participant progresses on nivolumab. The primary endpoint is the best overall response to nivolumab, using both Response Evaluation Criteria in Solid Tumours version 1.1 and immunotherapy modified Response Evaluation Criteria in Solid Tumours. Secondary endpoints include progression-free survival, overall survival, and quality of life.

DISCUSSION: ELEVATE will provide evidence for whether giving nivolumab after temozolomide in patients with previously treated advanced oesophagogastric adenocarcinoma is safe and biologically effective prior to future randomised trials.

TRIAL REGISTRATIONS: EudraCT Number: 2020-004771-41 (issued 01 October 2020); ISCRTN11398887 (registered 14 July 2021).

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Accepted/In Press date: 13 July 2022
Published date: 1 September 2022
Additional Information: © 2022. The Author(s).
Keywords: Immunotherapy, MGMT methylated, Oesophagogastric adenocarcinoma, Phase II

Identifiers

Local EPrints ID: 470274
URI: http://eprints.soton.ac.uk/id/eprint/470274
ISSN: 1471-2407
PURE UUID: c609d61b-eb32-494c-a1c6-ab488035f652
ORCID for Kelly Cozens: ORCID iD orcid.org/0000-0001-9592-9100
ORCID for Sean Ewings: ORCID iD orcid.org/0000-0001-7214-4917
ORCID for Tim Underwood: ORCID iD orcid.org/0000-0001-9455-2188
ORCID for Gareth Griffiths: ORCID iD orcid.org/0000-0002-9579-8021

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Date deposited: 05 Oct 2022 16:41
Last modified: 17 Mar 2024 03:36

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Contributors

Author: Elizabeth Smyth
Author: Kelly Cozens ORCID iD
Author: Daniel Griffiths
Author: Kathryn L Clark
Author: Sean Ewings ORCID iD
Author: Russell Petty
Author: Tim Underwood ORCID iD
Author: Rebecca C Fitzgerald
Author: James Tanner
Author: Olivier Giger
Author: Shubha Anand

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