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First-in-human Phase 1 CRISPR Gene Editing Cancer Trials: Are We Ready?
Baylis, Francoise; McLeod, Marcus.
Afiliación
  • Baylis F; Novel Tech Ethics, Faculty of Medicine, Dalhousie University, P.O. Box 15000, 1379 Seymour Street Halifax, NS, Canada.
  • McLeod M; Novel Tech Ethics, Faculty of Medicine, Dalhousie University, P.O. Box 15000, 1379 Seymour Street Halifax, NS, Canada.
Curr Gene Ther ; 17(4): 309-319, 2017.
Article en En | MEDLINE | ID: mdl-29173170
A prospective first-in-human Phase 1 CRISPR gene editing trial in the United States for patients with melanoma, synovial sarcoma, and multiple myeloma offers hope that gene editing tools may usefully treat human disease. An overarching ethical challenge with first-in-human Phase 1 clinical trials, however, is knowing when it is ethically acceptable to initiate such trials on the basis of safety and efficacy data obtained from pre-clinical studies. If the pre-clinical studies that inform trial design are themselves poorly designed - as a result of which the quality of pre-clinical evidence is deficient - then the ethical requirement of scientific validity for clinical research may not be satisfied. In turn, this could mean that the Phase 1 clinical trial will be unsafe and that trial participants will be exposed to risk for no potential benefit. To assist sponsors, researchers, clinical investigators and reviewers in deciding when it is ethically acceptable to initiate first-in-human Phase 1 CRISPR gene editing clinical trials, structured processes have been developed to assess and minimize translational distance between pre-clinical and clinical research. These processes draw attention to various features of internal validity, construct validity, and external validity. As well, the credibility of supporting evidence is to be critically assessed with particular attention to optimism bias, financial conflicts of interest and publication bias. We critically examine the pre-clinical evidence used to justify the first-inhuman Phase 1 CRISPR gene editing cancer trial in the United States using these tools. We conclude that the proposed trial cannot satisfy the ethical requirement of scientific validity because the supporting pre-clinical evidence used to inform trial design is deficient.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proyectos de Investigación / Ensayos Clínicos Fase I como Asunto / Sistemas CRISPR-Cas / Edición Génica / Neoplasias Tipo de estudio: Observational_studies / Risk_factors_studies Aspecto: Ethics Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Curr Gene Ther Asunto de la revista: GENETICA MEDICA / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Emiratos Árabes Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proyectos de Investigación / Ensayos Clínicos Fase I como Asunto / Sistemas CRISPR-Cas / Edición Génica / Neoplasias Tipo de estudio: Observational_studies / Risk_factors_studies Aspecto: Ethics Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Curr Gene Ther Asunto de la revista: GENETICA MEDICA / TERAPEUTICA Año: 2017 Tipo del documento: Article País de afiliación: Canadá Pais de publicación: Emiratos Árabes Unidos