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骨髓增生异常综合征介入临床试验参与率低且存在差异。

Low participation rates and disparities in participation in interventional clinical trials for myelodysplastic syndromes.

机构信息

Weatherall Institute of Molecular Medicine, Oxford, United Kingdom.

Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland, Ohio.

出版信息

Cancer. 2020 Nov 1;126(21):4735-4743. doi: 10.1002/cncr.33105. Epub 2020 Aug 7.

Abstract

BACKGROUND

The development of novel therapies for the myelodysplastic syndromes (MDS) is hampered by inadequate trial recruitment. Factors contributing to low trial accrual are incompletely understood.

METHODS

This study analyzed a pooled patient database from institutions of the US MDS Clinical Research Consortium to compare the characteristics of participants in interventional trials with those of patients who did not enroll in a trial.

RESULTS

Data were identified for 1919 patients with MDS, and 449 of these patients (23%) participated in an interventional clinical trial. The median age of all patients was 68 years, and 64% were male. Patients who participated in trials were significantly younger than nonparticipants (P = .014), and men were more likely to participate in a trial (71% of trial participants were male, whereas 61% of nonparticipants were; P < .001). Race and ethnicity were not associated with trial enrollment. Patients in more affluent ZIP codes had a higher participation rate (P < .001). Patients with intermediate- and high-risk disease according to the revised International Prognostic Scoring System were overrepresented (P = .004), and trial participants less frequently had treatment-related disease (P < .001). In multivariable analyses, participation in a clinical trial was associated with a reduced hazard of death (P = .004). Even at large referral centers, only a minority of patients with MDS enrolled in interventional trials.

CONCLUSIONS

Restrictive trial eligibility criteria that exclude patients with MDS on account of age, comorbidities, or a history of another cancer are limit enrollment of MDS patients to clinical trials. Gaining insight into the barriers to trial accrual may help investigators and study sponsors to design trials that will accrue more rapidly and augment treatment options for patients with MDS.

摘要

背景

新型疗法的研发对于骨髓增生异常综合征(MDS)受到了临床试验招募不足的阻碍。临床试验参与率低的原因尚未完全明确。

方法

本研究分析了美国 MDS 临床研究联合会机构的患者数据库,以比较干预性临床试验参与者和未参加临床试验的患者的特征。

结果

共纳入 1919 例 MDS 患者,其中 449 例(23%)患者参与了干预性临床试验。所有患者的中位年龄为 68 岁,64%为男性。参与临床试验的患者明显比未参与的患者年轻(P=0.014),男性更有可能参与临床试验(71%的试验参与者为男性,而非参与者中这一比例为 61%;P<0.001)。种族和民族与临床试验的参与无关。收入较高的邮政编码的患者参与率更高(P<0.001)。根据修订后的国际预后评分系统,中高危疾病的患者比例较高(P=0.004),并且试验参与者较少患有与治疗相关的疾病(P<0.001)。多变量分析显示,参与临床试验与降低死亡风险相关(P=0.004)。即使在大型转诊中心,也只有少数 MDS 患者参加了干预性临床试验。

结论

排除因年龄、合并症或其他癌症史而处于 MDS 高风险的患者的严格临床试验入组标准限制了 MDS 患者参加临床试验。深入了解临床试验参与的障碍可能有助于研究者和研究赞助商设计出能够更快入组并增加 MDS 患者治疗选择的试验。

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