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1
Recruitment to a prospective breast conservation trial: why are so few patients randomised?一项前瞻性保乳试验的招募情况:为何随机分组的患者如此之少?
BMJ. 1990 Jul 14;301(6743):83-5. doi: 10.1136/bmj.301.6743.83.
2
Psychological outcomes of different treatment policies in women with early breast cancer outside a clinical trial.非临床试验中早期乳腺癌女性不同治疗策略的心理结局
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3
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Ethical considerations in randomized controlled clinical trials.随机对照临床试验中的伦理考量
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Is there really an ethical conflict in clinical trials?
Cancer. 1995 May 15;75(10):2407-9; discussion 2410-1. doi: 10.1002/1097-0142(19950515)75:10<2407::aid-cncr2820751003>3.0.co;2-x.
7
Breast irradiation in women with early stage invasive breast cancer following breast conservation surgery. Provincial Breast Disease Site Group.保乳手术后早期浸润性乳腺癌女性的乳房放疗。省级乳腺疾病站点组。
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The National Cancer Institute audit of the National Surgical Adjuvant Breast and Bowel Project Protocol B-06.美国国立癌症研究所对国立乳腺与肠道外科辅助治疗项目协议B - 06的审计。
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BMJ Open. 2020 Mar 19;10(3):e034354. doi: 10.1136/bmjopen-2019-034354.
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Physician participation in clinical research and trials: issues and approaches.医生参与临床研究与试验:问题与方法
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Why don't women participate? A qualitative study on non-participation in a surgical randomised controlled trial.女性为何不参与?一项关于不参与外科随机对照试验的定性研究。
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Paying clinicians to join clinical trials: a review of guidelines and interview study of trialists.向临床医生支付参与临床试验的费用:指南综述及对试验人员的访谈研究
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Effects of patient selection on the applicability of results from a randomised clinical trial (EORTC 10853) investigating breast-conserving therapy for DCIS.患者选择对一项关于导管原位癌保乳治疗的随机临床试验(EORTC 10853)结果适用性的影响。
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本文引用的文献

1
Mastectomy or conservation: the patient's choice.乳房切除术还是保乳手术:由患者选择。
BMJ. 1988 Nov 5;297(6657):1167-9. doi: 10.1136/bmj.297.6657.1167.
2
Breast cancer therapy: exercising all our options.
N Engl J Med. 1989 Feb 23;320(8):527-9. doi: 10.1056/NEJM198902233200812.
3
Randomised trials and informed consent.
Lancet. 1988 Oct 29;2(8618):1033-4. doi: 10.1016/s0140-6736(88)90805-7.
4
Conservation therapy of breast cancer.
Lancet. 1989 Jul 15;2(8655):168-9. doi: 10.1016/s0140-6736(89)90237-7.
5
Patient preferences and randomised clinical trials.患者偏好与随机临床试验。
BMJ. 1989 Jul 29;299(6694):313-5. doi: 10.1136/bmj.299.6694.313.
6
Ethics of clinical research: lessons for the future.临床研究伦理:对未来的启示。
BMJ. 1989 Jul 22;299(6693):251-3. doi: 10.1136/bmj.299.6693.251.

一项前瞻性保乳试验的招募情况:为何随机分组的患者如此之少?

Recruitment to a prospective breast conservation trial: why are so few patients randomised?

作者信息

Jack W J, Chetty U, Rodger A

机构信息

Scottish Cancer Trials Office (MRC), Medical School, University of Edinburgh.

出版信息

BMJ. 1990 Jul 14;301(6743):83-5. doi: 10.1136/bmj.301.6743.83.

DOI:10.1136/bmj.301.6743.83
PMID:2390587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1663425/
Abstract

OBJECTIVE

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.

DESIGN

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.

SETTING

The breast unit, Longmore Hospital, Edinburgh, during 1988.

PATIENTS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

设计

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。

地点

1988年期间,爱丁堡朗莫尔医院乳腺科。

患者

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。

结果

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。

结论

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。