Schain W S
Cancer. 1994 Nov 1;74(9 Suppl):2666-71. doi: 10.1002/1097-0142(19941101)74:9+<2666::aid-cncr2820741814>3.0.co;2-p.
The reasons why less than 3% of cancer patients receive treatment in a clinical trial are complex and multiply determined. Because an individual cannot sign herself into a research study, an understanding of the doctor-patient interaction must be considered in addition to individual patient dynamics. Patients may be concerned that a physician's primary allegiance is to the requirements of the trial, not the specific health needs of the individual. Physicians may worry about the effects that placing an individual in a trial will have on the special doctor-patient relationship. Specific psychologic factors that may make a patient reluctant to enter a trial include self-protectiveness, time and travel constraints, concern about the quality of research versus clinical care, the nature of the informed consent, and worry about the usual low level priority assigned to quality-of-life issues in biomedical research. Enrollment in and adherence to investigative research may be served better by the construction of studies that combine questions about both medical outcome and impact of treatment on patient quality of life. Individuals who require high levels of personal control, want to feel they are a high priority with their physician, and need frequent feedback about results are not likely to be good candidates for investigative research.
不到3%的癌症患者在临床试验中接受治疗,其原因复杂且由多种因素共同决定。由于个人无法自行参与研究,除了患者个体因素外,还必须考虑医患互动情况。患者可能担心医生首要遵循的是试验要求,而非个人的具体健康需求。医生可能担心让患者参与试验会对特殊的医患关系产生影响。可能使患者不愿参与试验的具体心理因素包括自我保护意识、时间和出行限制、对研究质量与临床护理质量的担忧、知情同意的性质,以及对生物医学研究中生活质量问题通常被置于低优先级的担忧。构建同时兼顾医学结果和治疗对患者生活质量影响问题的研究,可能更有助于提高参与调查研究的人数及依从性。那些需要高度个人掌控感、希望觉得自己在医生那里是高度优先考虑对象且需要频繁了解结果反馈的人,不太可能是调查研究的理想人选。