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iSITE: Investigation of Somatic Alterations in Tumours of the Eye

T

The Wellcome Sanger Institute

Status

Completed

Conditions

Somatic Mutation
Ocular Melanoma

Treatments

Other: Blood Sample
Other: sample collection
Other: Discussing study/seeking consent
Other: Completion of Study Questionnaire

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Modern DNA sequencing technologies enable researchers to identify mutations that have been acquired during the lifetime of patients (somatic mutations). Some of these somatic mutations occur in cancer genes and increase the risk of developing cancer. This study will apply such sequencing technologies to cancers of the eye (ocular melanoma) in order to identify mutations associated with these cancers. Sequencing patients at different stages of their disease will allows us to build a timeline of the order of mutations that occur at each stage. This information can be used to understand how these cancers develop, spread (metastasise) and respond to treatment. Furthermore, the study will look at which of these somatic mutations are present in the blood, by collecting blood samples and sequencing fragments of DNA which have been released by tumours into the bloodstream (circulating tumour DNA, ctDNA). This will determine whether ctDNA can be used as a way of monitoring mutations present in the tumour. This study will provide much needed insight into a rare and understudied cancer type, with the long-term aim of improving the survival of patients by identifying key mutations to develop novel therapies against.

Full description

Uveal melanomas are rare cancers that arise from pigment cells (melanocytes) in the eye. Like most rare cancers, limited interest in developing new therapies and a lack of clinical trials contributes towards relatively worse survival rates compared with common cancers. Following treatment of uveal melanoma with either surgical removal of the eye (enucleation) or local radiation (plaque brachytherapy), approximately half of all patients will develop metastases (new tumours). Most patients will die within a few months despite current therapies.

Conjunctival melanomas (cancer of the surface of the eye which lines the inside of the eyelids) are an extremely rare subset of eye cancers which also have poor survival outcomes once metastasised. Modern DNA sequencing technologies enable researchers to identify mutations acquired during the lifetime of an individual (these are known as somatic mutations). Some of these somatic mutations occur in cancer-associated genes, and increase the risk of developing cancer. This study will use sequencing technologies to look to identify mutations associated with cancers of the eye. By sequencing at different stages of the disease we hope to build a timeline of the order of mutations that occur during eye cancer development. The investigators will also generate cell line models to try and understand how these cancers develop, spread (metastasise) and respond to treatments. The investigators will also look at which somatic mutations are detectable in blood. Blood samples will be collected regularly from participants and circulating tumour DNA, (ctDNA, fragments of DNA released by tumours into the bloodstream) will be sequenced. The investigators will determine whether the mutations present in ctDNA can be used as an indicator of disease progression.

This study will provide much needed insight into a rare and understudied cancer type, with the aim of improving the survival of patients by identifying key mutations to develop novel therapies against.

Enrollment

70 patients

Sex

All

Ages

18 to 99 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients ≥ 18 years of age or over

  • Histological diagnosis of primary or recurrent/metastatic ocular melanoma*.

  • Healthy eye, blood and liver samples stored in biobanks with consent for use in research.

    • *With the exception of primary uveal melanoma where a clinical diagnosis is sufficient. A diagnostic accuracy of >99% is achieved using the combination of ophthalmoscopy (examination of the back of the eye), fundus photography (photograph of the back of the eye) and an eye ultrasound.

Exclusion criteria

  • Patients < 18 years of age

Trial design

70 participants in 4 patient groups

A (Primary uveal melanoma)
Description:
Prospective collection, primary uveal melanoma. If patients have previously collected samples, consent will be requested to also obtain these samples.
Treatment:
Other: Completion of Study Questionnaire
Other: Discussing study/seeking consent
Other: sample collection
Other: Blood Sample
B1 (Metastatic uveal melanoma)
Description:
Prospective collection, metastatic uveal melanoma. If patients have previously collected samples, consent will be requested to also obtain these samples.
Treatment:
Other: Completion of Study Questionnaire
Other: Discussing study/seeking consent
Other: sample collection
Other: Blood Sample
B2 (Metastatic uveal melanoma, precollected only)
Description:
Previously collected and stored tissue samples, retrospective collection only, metastatic uveal melanoma
C (Conjunctival melanoma)
Description:
Previously collected and stored tissue samples, retrospective collection only, metastatic conjunctival melanoma ,

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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