John Lee

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Associate Professor-in-Residence

University of California, Los Angeles
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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)

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2023

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2023

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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

UNITED STATES
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Daniel Chen

Fred Hutchinson Cancer Research Center

UNITED STATES
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Alexander Xu

Assistant Professor

University of Maryland at College Park

UNITED STATES
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Gavin Ha

Assistant Professor

Fred Hutchinson Cancer Research Center

UNITED STATES
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SANDIPAN BRAHMA

Assistant Professor

University of Nebraska Medical Center

UNITED STATES
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Philippe Depeille

Adjunct assistant professor (ATER)

University of Montpellier

FRANCE
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Christopher Seet

Assistant Professor

David Geffen School of Medicine at UCLA

UNITED STATES
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Bruce Montgomery

University of Washington

UNITED STATES
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Weixian Deng

David Geffen School of Medicine at UCLA

UNITED STATES
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Koichi Sasaki

Imperial College London

UNITED KINGDOM
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James Heath

Professor

California Institute of Technology

UNITED STATES
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