John Lee
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Associate Professor-in-Residence
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John Lee is an Associate Professor-in-Residence at the University of California, Los Angeles, USA. His research areas include T cell receptor gene therapy, immunotherapy for advanced prostate cancer, and genomic characterization of cancer. He has contributed to significant studies on antigen-specific T cell discovery and the barriers to cancer progression, reflecting his expertise in cancer immunology and therapeutic development.
Recent Grants
Grant: Close
Targeting the cell surfaceome of aggressive neuroendocrine prostate cancer
Open Date: 2017-07-01
Close Date: 2021-06-01
Articles (10)
Year:
2023
Year:
2023
Year:
2023
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2023
PURPOSE Germline mutations in DNA repair genes are present in approximately 10% of men with metastatic prostate cancer (mPC), and guidelines recommend genetic germline testing. Notable barriers exist, including access to genetic counseling, insurance coverage, and out-of-pocket costs. The GENTleMEN study was designed to determine the feasibility of an Internet-based, patient-driven germline genetic testing approach for men with mPC. PATIENTS AND METHODS In this prospective cohort study, men with mPC provided informed consent via an Internet-based platform and completed a questionnaire including demographics and family cancer history. Supporting medical data were also collected. Genetic testing was performed using the Color Genomics 30-gene targeted panel of cancer predisposition genes on a mailed saliva sample. Men whose test results identified a germline pathogenic or likely pathogenic variant received results by phone or telehealth genetic counseling; other participants received results by email with an option for phone-based or telehealth genetic counseling. RESULTS As of August 18, 2021, 816 eligible men were consented, of whom 68% (551) completed genetic testing, and 8.7% (48 of 551) were found to carry a pathogenic or likely pathogenic variant in a germline DNA repair gene: CHEK2 (17), BRCA2 (15), ATM (6), NBN1 (3), BRCA1 (2), PALB2 (2), PMS2 (2), and MSH6 (1). Participants were more likely to complete the testing process if they were non-Hispanic White, married, highly educated, or from a higher-income bracket. CONCLUSION Here, we show the feasibility of delivering germline (inherited) genetic testing by a voluntary, patient-driven, Internet-based platform to men with mPC. Preliminary results show rates of germline DNA repair mutations, consistent with other cohorts. Although feasible for some, reduced steps for participation, more dedicated diverse outreach and participant support, and identification and addressing of additional barriers is needed to ensure equitable access and optimization.
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2023
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2023
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2023
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2022
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2022
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2022
Collaborators (11)
David A. Quigley
University of California, San Francisco
Daniel Chen
Fred Hutchinson Cancer Research Center
Alexander Xu
Assistant Professor
University of Maryland at College Park
Gavin Ha
Assistant Professor
Fred Hutchinson Cancer Research Center
SANDIPAN BRAHMA
Assistant Professor
University of Nebraska Medical Center
Philippe Depeille
Adjunct assistant professor (ATER)
University of Montpellier
Christopher Seet
Assistant Professor
David Geffen School of Medicine at UCLA
Bruce Montgomery
University of Washington
Weixian Deng
David Geffen School of Medicine at UCLA
Koichi Sasaki
Imperial College London
James Heath
Professor
California Institute of Technology
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