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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05734963
Other study ID # CCR5396
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 4, 2022
Est. completion date April 12, 2031

Study information

Verified date February 2023
Source Royal Marsden NHS Foundation Trust
Contact Ben O'Leary
Phone 02071535337
Email ben.oleary@icr.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

ORIGINS - a multi-site sample collection study to establish patient-derived pre-clinical models for cancers


Description:

People who develop cancer can often be cured if they are suitable for surgery or radiotherapy. However, a proportion of these cancers return, at which point the available treatment options are often not very effective. Our understanding of the biology of many cancers is limited, and we don't understand why some cancers are cured by surgery or radiotherapy and some are not. A better understanding of the biology of cancers could help develop new treatments, or improvements to current treatments, and this might increase the number of patients who can be cured of their disease. One way to improve the understanding we have of the biology is to look in detail at cancer samples taken from the from patients. The problem with this is that often samples are small, and the tumour tissue sample itself already dead once removed from where it was growing, which can limit the analyses that are possible. A potential solution for this is to take cancer tissue from patients and try to directly grow the cells in the laboratory. Keeping the cancer cells alive in the laboratory can be difficult but has been shown to be possible in a number of different types of cancer. This kind of model is sometimes known as an "organoid". If successfully established, it means more tests can be done to find out how the cancer is working. This study is looking at collecting samples of a person's cancer to see if we can develop these models from patients being treated for different cancers. We will ask people who are having surgery for cancer whether we can take samples from their tumour to try and achieve this. Some additional blood tests will be taken alongside the usual blood tests before and after surgery, without an additional blood draw, and before and again after any adjuvant therapy is completed. A collection of saliva will also be requested at these times and we will ask people whether they are happy for us to collect any previous tissue samples, or nay that are subsequently collected when they are being followed up, to allow comparison with the samples collected as part of this study. The main goal of this study is to see if organoids can be established in our laboratories. If these models are successfully established, we will compare them to the original tumour to check they are a good match biologically. After this we can use them to understand how the cancer works and try out new treatments.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date April 12, 2031
Est. primary completion date April 12, 2031
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years or older - Patients with histologically proven or suspected cancer undergoing an interventional procedure, such as surgery or biopsy - Ability to give informed consent for biological sample collection Exclusion Criteria: - Unable to undergo sample collection - Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
DNA sequencing, RNA gene expression analysis, molecular profiling
Growth of organoids from tissue samples, collection of tissue, blood and saliva samples for DNA sequencing, RNA gene expression analysis, molecular profiling

Locations

Country Name City State
United Kingdom The Royal Marsden Hospital London

Sponsors (1)

Lead Sponsor Collaborator
Royal Marsden NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Establish patient-derived organoid (PDO) model for cancers Establish patient-derived organoid (PDO) model for cancers Time Frame: Through study completion, expected duration of 9 years
Secondary To collection contemporaneous biological samples from patients with cancer before and after surgery/biopsy, and again after any adjuvant therapy To collection contemporaneous biological samples from patients with cancer before and after surgery/biopsy, and again after any adjuvant therapy - including blood, saliva and tissue, for molecular profiling, including extraction of DNA for sequencing, RNA Time Frame: Through study completion, expected duration of 9 years
Secondary To collect tumour tissue to facilitate evolutionary analysis with molecular analysis of multiple regions Time Frame: Through study completion, expected duration of 9 years
Secondary Retrieval and analysis of archival primary tissue blocks for comparison where available Time Frame: Through study completion, expected duration of 9 years
Secondary To establish co-culture tumour/stroma/immune cell models Time Frame: Through study completion, expected duration of 9 years
Secondary To observe associations between molecular and clinicopathological data Time Frame: Through study completion, expected duration of 9 years
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