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胰腺癌临床治疗试验入组:参与率的深入观察。

Pancreatic Cancer Clinical Treatment Trials Accrual: A Closer Look at Participation Rates.

机构信息

Departments of Medicine.

Abramson Cancer Center of the University of Pennsylvania, Philadelphia, PA.

出版信息

Am J Clin Oncol. 2021 Jun 1;44(6):227-231. doi: 10.1097/COC.0000000000000807.

DOI:10.1097/COC.0000000000000807
PMID:33710138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8140996/
Abstract

OBJECTIVES

Low rates of participation in cancer clinical trials are commonly reported, raising concerns about missed opportunities to engage patients in treatment trials. We reviewed eligibility for and enrollment in pancreatic cancer clinical trials for patients seen at a National Cancer Institute (NCI)-designated cancer center during 1 year, to calculate participation rates with detailed information to determine the best-case participation rate.

MATERIALS AND METHODS

This retrospective cohort study used the Abramson Cancer Center Cancer Registry, clinical trial protocols, and electronic medical records (EMRs) to determine eligibility for all available pancreatic cancer clinical trials. Patient characteristics and reasons for ineligibility were abstracted from EMRs. We then computed participation rates based on enrollment in trials using EMR and clinical trials monitoring data.

RESULTS

Of 233 new pancreatic cancer patients in 2014, 47 or 20% enrolled in a clinical trial (enrollment fraction). According to the EMR, of the 66 patients who were eligible for a trial, 54 (82% of eligible) accepted and 47 (71% of eligible) ultimately enrolled in a trial, 8 (12% of eligible) declined, and 4 (6% of eligible) had no record of patient decision. Enrollment in a trial by both the EMR and clinical trials database was confirmed for 71% of eligible patients.

CONCLUSIONS

This study reveals that 71% of newly diagnosed pancreatic cancer patients who were eligible for a trial were enrolled in a treatment trial. We contend that in-depth analysis, rather than enrollment fraction, should be used to inform the gap between actual participation and optimal clinical trial participation for cancer patients.

摘要

目的

癌症临床试验的参与率普遍较低,这引发了人们对患者错失参与治疗试验机会的担忧。我们回顾了在 1 年内,在国立癌症研究所(NCI)指定的癌症中心就诊的胰腺癌患者参与临床试验的资格和入组情况,计算了详细信息的参与率,以确定最佳参与率。

材料与方法

这项回顾性队列研究使用了艾布拉姆森癌症中心癌症登记处、临床试验方案和电子病历(EMR)来确定所有可用胰腺癌临床试验的资格。从 EMR 中提取患者特征和不合格原因。然后,我们根据 EMR 和临床试验监测数据计算了参与试验的比例。

结果

在 2014 年的 233 名新胰腺癌患者中,47 名或 20%(入组率)入组了临床试验。根据 EMR,在 66 名有资格参加试验的患者中,有 54 名(合格患者的 82%)接受了试验,47 名(合格患者的 71%)最终入组了试验,8 名(合格患者的 12%)拒绝了试验,4 名(合格患者的 6%)没有记录患者的决定。通过 EMR 和临床试验数据库确认了 71%有资格参加试验的患者入组了试验。

结论

这项研究表明,71%有资格参加试验的新诊断胰腺癌患者入组了治疗试验。我们认为,应该深入分析,而不是仅仅计算入组率,以了解癌症患者实际参与和最佳临床试验参与之间的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8737/8140996/ae7ce8419fd5/nihms-1672846-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8737/8140996/ae7ce8419fd5/nihms-1672846-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8737/8140996/ae7ce8419fd5/nihms-1672846-f0001.jpg

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