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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01925599
Other study ID # BAP101
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 2013
Est. completion date January 2022

Study information

Verified date March 2021
Source Greater Houston Retina Research
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The BAP1 trial will examine the blood of patients diagnosed with choroidal nevi or uveal melanoma for a germline BAP1 mutation and other genetic markers associated with developing malignancy as well as additional sequencing of the uveal melanoma genome.


Description:

A germline BAP1 mutation predisposes a person to developing uveal melanoma and other cancers. If a mutation is discovered, it changes the potential approach to managing the nevus. In the presence of a known genomic change associated with aggressive disease, closer follow up and more aggressive treatment could preserve the patient's vision and prevent micrometastatic spread. This new screening technique will be able to extend the length and quality of life of patients with more frequent targeted cancer screens.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 133
Est. completion date January 2022
Est. primary completion date January 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: any person with choroidal nevi - Willingness to provide signed informed consent - Age > 18 years - Diagnosis of choroidal nevi or uveal melanoma Threre are no exclusionary criteria for this study.

Study Design


Locations

Country Name City State
United States Retina Consultants of Houston Houston Texas
United States Retina Consultants of Houston Katy Texas
United States Retina Consultants of Houston The Woodlands Texas

Sponsors (1)

Lead Sponsor Collaborator
Amy C Schefler, MD

Country where clinical trial is conducted

United States, 

References & Publications (6)

Abdel-Rahman MH, Pilarski R, Cebulla CM, Massengill JB, Christopher BN, Boru G, Hovland P, Davidorf FH. Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers. J Med Genet. 2011 Dec;48(12):856-9. doi: 10.1136/jmedgenet-2011-100156. Epub 2011 Sep 22. — View Citation

Jensen DE, Rauscher FJ 3rd. Defining biochemical functions for the BRCA1 tumor suppressor protein: analysis of the BRCA1 binding protein BAP1. Cancer Lett. 1999 Sep;143 Suppl 1:S13-7. Review. — View Citation

Matatall KA, Agapova OA, Onken MD, Worley LA, Bowcock AM, Harbour JW. BAP1 deficiency causes loss of melanocytic cell identity in uveal melanoma. BMC Cancer. 2013 Aug 5;13:371. doi: 10.1186/1471-2407-13-371. — View Citation

Singh AD, Kalyani P, Topham A. Estimating the risk of malignant transformation of a choroidal nevus. Ophthalmology. 2005 Oct;112(10):1784-9. Review. — View Citation

Singh AD, Turell ME, Topham AK. Uveal melanoma: trends in incidence, treatment, and survival. Ophthalmology. 2011 Sep;118(9):1881-5. doi: 10.1016/j.ophtha.2011.01.040. Epub 2011 Jun 24. Review. — View Citation

Ventii KH, Devi NS, Friedrich KL, Chernova TA, Tighiouart M, Van Meir EG, Wilkinson KD. BRCA1-associated protein-1 is a tumor suppressor that requires deubiquitinating activity and nuclear localization. Cancer Res. 2008 Sep 1;68(17):6953-62. doi: 10.1158/0008-5472.CAN-08-0365. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Examine the rate of germline BAP1 mutations in young patients, diagnosed with choroidal nevi 1 Year