Predicting Response to Immunotherapy for Melanoma With Gut Microbiome and Metabolomics

NCT ID: NCT03643289

Last Updated: 2020-02-27

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

450 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-04-04

Study Completion Date

2023-05-02

Brief Summary

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This study will investigate the effects of gut microbiome diversity (richness in terms of many bacterial species in the gut) on responses and side effects of immunotherapy in advanced melanoma patients. Immunotherapy for melanoma is especially damaging for the gut with colitis which can lead to death and significant morbidity with repeated hospital admissions. The richness of the microbiome in the gut may be protective against colitis and other side effects but this needs to be confirmed. There is also some preliminary evidence that the gut microbiome diversity can enhance responses to immunotherapy in cancer but this has been shown in small numbers of melanoma patients.

Detailed Description

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This pilot project will assess the gut microbiome with metagenome sequencing before and after starting immunotherapy in stage 3 and 4 melanoma patients. The project will assess the impact of the gut microbiome on treatment response rates and side effects induced by immunotherapy.

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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Melanoma (Skin)

Study Design

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Observational Model Type

COHORT

Study Time Perspective

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

\- Patients aged over the age of 18 years with advanced melanoma due to receive first line systemic treatment with immunotherapy with a checkpoint inhibitor alone or in combination.

Exclusion Criteria

* Patients who have had systemic anti-cancer treatment for locally advanced or metastatic disease.
* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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King's College London

OTHER

Sponsor Role collaborator

East and North Hertfordshire NHS Trust

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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East and North Hertfordshire NHS Trust

Northwood, Middlesex, United Kingdom

Site Status RECRUITING

Guy's and St. Thomas' NHS Foundation Trust

London, , United Kingdom

Site Status RECRUITING

The Christie NHS Foundation Trust

Manchester, , United Kingdom

Site Status RECRUITING

The Clatterbridge Cancer Centre

Metropolitan Borough of Wirral, , United Kingdom

Site Status RECRUITING

Lancashire Teaching Hospitals NHS Foundation Trust

Preston, , United Kingdom

Site Status RECRUITING

Countries

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United Kingdom

Central Contacts

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Clare Stockwell

Role: CONTACT

02071887188 (x86754)

Paul Nathan

Role: CONTACT

0203 826 2444

Facility Contacts

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Paul Nathan

Role: primary

02038262444

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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