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Physician Recruitment of Patients to Non-Therapeutic Oncology Clinical Trials: Ethics Revisited

机译:接受非治疗肿瘤学临床试验的医师招募:重新考虑伦理

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摘要

Tailoring medical treatment to individual patients requires a strong foundation in research to provide the data necessary to understand the relationship between the disease, the patient, and the type of treatment advocated for. Non-therapeutic oncology clinical trials studying therapeutic resistance require the participation of patients, yet only a small percentage enroll. Treating physicians are often relied on to recruit patients, but they have a number of ethical obligations that might be perceived as barriers to recruiting. Concepts such as voluntariness of consent and conflicts of interest can have an impact on whether physicians will discuss clinical trials with their patients and how patients perceive the information. However, these ethical obligations should not be prohibitive to physician recruitment of patients – precautions can be taken to ensure that patients’ consent to research participation is fully voluntary and devoid of conflict, such as the use of other members of the research team than the treating physician to discuss the trial and obtain consent, and better communication between researchers, clinicians, and patients. These can ensure that research benefits are maximized for the good of patients and society.
机译:为个别患者量身定制药物治疗需要坚实的研究基础,以提供必要的数据来理解疾病,患者和所主张的治疗类型之间的关系。研究治疗耐药性的非治疗肿瘤学临床试验需要患者参与,但只有很小的比例参加。通常依靠治疗医生招募患者,但是他们有许多道德义务,可能被视为招募的障碍。自愿同意和利益冲突等概念可能会影响医生是否会与患者讨论临床试验以及患者如何理解信息。但是,这些道德义务不应禁止医师招募患者–可以采取预防措施以确保患者同意参加研究是完全自愿的,并且没有冲突,例如使用研究团队以外的其他成员来治疗患者医师讨论试验并获得同意,并在研究人员,临床医生和患者之间进行更好的沟通。这些可以确保最大程度地为患者和社会造福研究收益。

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