Predicting Response to Immunotherapy for Melanoma With Gut Microbiome and Metabolomics
NCT ID: NCT03643289
Last Updated: 2020-02-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
450 participants
OBSERVATIONAL
2018-04-04
2023-05-02
Brief Summary
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Detailed Description
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200 stage 4 and 250 stage 3 melanoma patients naive to immunotherapy will be recruited from melanoma clinics. Stool samples will be donated pre-treatment and at follow-up visits throughout treatment. An additional sample will also be requested in the event of disease progression or toxicity necessitating treatment delay or discontinuation. An accompanying stool sample questionnaire will be completed at each sampling time point with the optional completion of a 24-hour recall food diary.
Blood samples will also be taken before and after starting immunotherapy treatment, with gastrointestinal, food frequency, quality of life questionnaires administered at baseline. An optional tumour biopsy if safe and accessible, is requested from patients in the stage 4 cohort before and after starting immunotherapy.
Microbiome data from melanoma patients will be compared with the TwinsUK healthy control gut microbiome data on more than 3000 healthy adults. This analysis will help us assess if there are major differences between the microbiome composition in the melanoma cases prior to therapy compared to the control gut microbiome data from TwinsUK.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Cohort A
Patients with stage 4 melanoma due to commence immunotherapy. Patients should be naïve to immunotherapy.
No interventions assigned to this group
Cohort B
Patients with stage 3 melanoma who are naïve to immunotherapy
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients unable to consent because of language barrier or inability to consent.
* Patients unable to collect or send the stool samples for geographical, social or psychological reasons.
* Persons benefitting from protection system of adults (including guardianship and curatorship)
* Pregnant or breastfeeding women
18 Years
ALL
No
Sponsors
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King's College London
OTHER
East and North Hertfordshire NHS Trust
OTHER_GOV
Responsible Party
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Locations
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East and North Hertfordshire NHS Trust
Northwood, Middlesex, United Kingdom
Guy's and St. Thomas' NHS Foundation Trust
London, , United Kingdom
The Christie NHS Foundation Trust
Manchester, , United Kingdom
The Clatterbridge Cancer Centre
Metropolitan Borough of Wirral, , United Kingdom
Lancashire Teaching Hospitals NHS Foundation Trust
Preston, , United Kingdom
Countries
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Central Contacts
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Facility Contacts
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Mark Harries
Role: primary
Paul Lorrigan
Role: primary
Joseph Sacco
Role: primary
Ruth Board
Role: primary
Other Identifiers
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RD2016-56
Identifier Type: -
Identifier Source: org_study_id
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