Lemieux Julie, Forget Geneviève, Brochu Olyvia, Provencher Louise, Cantin Guy, Desbiens Christine, Doyle Catherine, Poirier Brigitte, Camden Stéphanie, Durocher Martin
Centre des Maladies du Sein Deschênes-Fabia, Hôpital du Saint-Sacrement, Centre hospitalier universitaire de Québec, 1050 chemin Sainte-Foy, Québec City, QC G1S 4L8, Canada; Centre hospitalier universitaire de Québec, Canada; Faculté de médecine, Université Laval, Québec, QC G1V 0A6, Canada.
Faculté de médecine, Université Laval, Québec, QC G1V 0A6, Canada.
Breast. 2014 Aug;23(4):385-92. doi: 10.1016/j.breast.2014.02.002. Epub 2014 Mar 26.
Objectives of the study were to measure recruitment rates in clinical trials and to identify patients, physicians or trials characteristics associated with higher recruitment rates. Among patients who had a clinical trial available for their cancer, 83.5% (345/413) met the eligibility criteria to at least one clinical trial. At least one trial was proposed to 33.1% (113/341) of the eligible patients and 19.7% (68/345) were recruited. Overall recruitment was 16.5% (68/413). In multivariate analyses, trial proposal and enrollment were lower for elderly patients and higher in high cancer stages. Trials from pharmaceutical industry had higher recruitment rates and trials testing hormonal therapy enrolled more patients. Breast cancer patients' accrual to a clinical trial could be improved by trying to systematically identify all eligible patients and propose a trial to those eligible and to whom the treatment is planned to be equivalent to the standard arm of the trial.
该研究的目的是衡量临床试验中的招募率,并确定与较高招募率相关的患者、医生或试验特征。在患有可参与其癌症临床试验的患者中,83.5%(345/413)符合至少一项临床试验的入选标准。至少一项试验被推荐给33.1%(113/341)的符合条件的患者,19.7%(68/345)的患者被招募。总体招募率为16.5%(68/413)。在多变量分析中,老年患者的试验推荐和入组率较低,而癌症晚期患者的试验推荐和入组率较高。制药行业开展的试验招募率较高,测试激素疗法的试验招募的患者更多。通过尝试系统地识别所有符合条件的患者,并向那些符合条件且计划接受的治疗与试验标准组等效的患者推荐试验,可以提高乳腺癌患者参与临床试验的入组率。