Jack W J, Chetty U, Rodger A
Scottish Cancer Trials Office (MRC), Medical School, University of Edinburgh.
BMJ. 1990 Jul 14;301(6743):83-5. doi: 10.1136/bmj.301.6743.83.
To investigate the rate of recruitment to early breast cancer trials and elucidate the reasons for ineligibility and refusal to participate among patients otherwise suitable for these trials.
Prospective study of one year's cohort of patients referred to a breast unit with special reference to the subgroup suitable for conservation management and to the proportion eligible for and (after informed consent) ultimately randomised within the Scottish early breast cancer trials.
The breast unit, Longmore Hospital, Edinburgh, during 1988.
All 3054 patients referred to the breast unit during the year. 324 Found to have invasive breast cancer and 147 initially thought suitable for conservation management.
63 Patients were treated by mastectomy, 19 of whom requested mastectomy rather than conservation management. 84 Patients were excluded from trials, and of the 63 eligible patients, 40 gave informed consent. Most of the 23 patients who refused the trials requested a specific adjuvant treatment after discussion of their management and the trials.
Recruitment to prospective trials in which informed consent is required before randomisation may be slower than predicted because of a high proportion of exclusions and also refusal by patients. Trials may therefore take longer to complete and give distorted results by virtue of the unpredictable nature of the selection of patients.
调查早期乳腺癌试验的招募率,并阐明适合这些试验的患者中不符合入选标准及拒绝参与的原因。
对转诊至乳腺科的一组为期一年的患者进行前瞻性研究,特别关注适合保乳治疗的亚组以及在苏格兰早期乳腺癌试验中符合入选标准并(在获得知情同意后)最终被随机分组的比例。
1988年期间,爱丁堡朗莫尔医院乳腺科。
该年度转诊至乳腺科的所有3054名患者。324例被发现患有浸润性乳腺癌,147例最初被认为适合保乳治疗。
63例患者接受了乳房切除术,其中19例要求进行乳房切除术而非保乳治疗。84例患者被排除在试验之外,在63例符合入选标准的患者中,40例签署了知情同意书。在23例拒绝试验的患者中,大多数在讨论了其治疗方案和试验后要求进行特定的辅助治疗。
由于排除比例高以及患者拒绝,在随机分组前需要获得知情同意的前瞻性试验的招募速度可能比预期的要慢。因此,试验可能需要更长时间才能完成,并且由于患者选择的不可预测性而得出扭曲的结果。