Generation Of a Lung Biobank for Future Use

NCT ID: NCT05234138

Last Updated: 2022-02-10

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

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-10-31

Study Completion Date

2023-10-31

Brief Summary

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The aim is to invite 1,000 patients with symptoms triggering the lung cancer diagnostic pathway or with significant risks of lung cancer, referred to The Royal Marsden NHS Foundation Trust (RMH) referral centres (Kingston Hospital NHS Foundation Trust, Epsom and St Helier University Hospitals NHS Trust, Croydon University Hospitals NHS Foundation Trust or St George's University Hospitals NHS Foundation Trust) over a 1 year period, to complete a life style questionnaire, document lung function tests and to donate a blood sample for storage with a view to testing for a genetic signature and other biomarkers in future studies from this established biobank.

Detailed Description

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Patients will have been referred under the two week rule (TWR) diagnostic pathway, some will have lung cancer, others not, and other patients will have had a diagnosis of lung cancer by other pathways i.e. non TWR.

There are 3 groups of patients:

Group A - lung cancer patients at any stage and by any non TWR pathway, n=250. Group B - lung cancer patients who were referred initially by the TWR pathway, n=150.

Group C - Subjects referred by the TWR pathway (i.e. with symptoms) who do not have lung cancer, or subjects referred by any pathway who do not have lung cancer but do have radiological changes (that need follow up) or a strong family history of lung cancer, n=600.

A strong family history for this study means 1 or more first degree relatives with lung cancer with at least one individual having lung cancer at age \<50 yrs.

Conditions

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Cancer Lung Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Blood Sample

Blood Sample

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

One of the following criteria:

* Patients with lung cancer at any stage or time in their disease.
* Patients without lung cancer who have been referred by the TWR pathway.
* Patients without lung cancer who have radiological changes on their X-Ray or CT scan that need follow up.
* Patients without lung cancer who have a strong family history of lung cancer. PLUS
* Patients aged \>18 Years
* Patients who have signed informed consent form

Exclusion Criteria

* Unable to provide informed consent.
* Bleeding disorder or other medical condition that would make a blood sample hazardous.
* Within 3 weeks of chemotherapy or radiotherapy (as low lymphocyte may be associated with poor DNA yield).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Royal Marsden NHS Foundation Trust

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Royal Marsden Hospital NHS Foundation Trust

London, , United Kingdom

Site Status RECRUITING

Countries

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United Kingdom

Central Contacts

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Mary O'Brien

Role: CONTACT

020 8642 6011

Facility Contacts

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Ann Gandolfi

Role: primary

02086613903

Other Identifiers

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CCR4977

Identifier Type: -

Identifier Source: org_study_id

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