首页> 外文期刊>Quality of life research: An international journal of quality of life aspects of treatment, care and rehabilitation >Patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE): emerging developments and practical approaches to collection and analysis of pro-based symptomatic adverse event data in cancer clinical trials

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Patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE): emerging developments and practical approaches to collection and analysis of pro-based symptomatic adverse event data in cancer clinical trials

机译：患者报告的不良事件通用术语标准的结果版本（PRO-CTCAE）：在癌症临床试验中收集和分析基于赞成症状的不良事件数据的新兴发展和实用方法

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《Quality of life research: An international journal of quality of life aspects of treatment, care and rehabilitation》 |2016年第1期|共1页
作者
Mitchell Sandra A.; Basch Ethan; Walding Andrew S.; Dueck Amylou C.;
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正文语种 eng
中图分类医药、卫生;
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入库时间 2022-08-18 17:11:49

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1. Patient-reported outcomes version of the common terminology criteria for adverse events (PRO-CTCAE): emerging developments and practical approaches to collection and analysis of pro-based symptomatic adverse event data in cancer clinical trials [J] . Mitchell Sandra A., Basch Ethan, Walding Andrew S., Quality of life research: An international journal of quality of life aspects of treatment, care and rehabilitation . 2016,第Suppla1期

机译：患者报告的不良事件通用术语标准的结果版本（PRO-CTCAE）：在癌症临床试验中收集和分析基于赞成症状的不良事件数据的新兴发展和实用方法
2. Feasibility of Patient Reporting of Symptomatic Adverse Events via the Patient-Reported Outcomes Version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) in a Chemoradiotherapy Cooperative Group Multicenter Clinical Trial [J] . Basch Ethan, Pugh Stephanie L., Dueck Amylou C., International Journal of Radiation Oncology, Biology, Physics . 2017,第2期

机译：患者通过患者报告的成果版本的常见术语标准的患者报告患者报告的不良事件（Pro-CTCAE）在化学疗法合作组多中心临床试验中的常见术语标准
3. The effect of surveillance for symptomatic toxicities with real-time clinician reporting on dose reduction, hospitalization and febrile neutropenia in Danish breast cancer patients-a population-based cluster randomized trial using the Patient-Reported Outcomes version of Common Terminology Criteria for Adverse Events (PRO-CTCAE) [J] . Pappot H., Baeksted C., Nissen A., European journal of cancer: official journal for European Organization for Research and Treatment of Cancer (EORTC) [and] European Association for Cancer Research (EACR) . 2018,第期

机译：症状毒性监测对丹麦乳腺癌患者剂量减少，住院和发热中性粒子的实时临床医生 - 一种使用患者报告的不良事件的常见术语标准的基于人群的群体随机试验（Pro -ctcae）
4. Machine Learning-Based Modeling of Big Clinical Trials Data for Adverse Outcome Prediction: A Case Study of Death Events [C] . Ling Tong, Jake Luo, Ron Cisler, IEEE Annual Computer Software and Applications Conference . 2019

机译：基于机器学习的不良结果预测的大型临床试验数据建模：死亡事件的案例研究
5. Hypersensitivity Adverse Event Reporting in Clinical Cancer Trials: Barriers and Potential Solutions to Studying Severe Events on a Population Level [D] . ?Eldredge, Christina 2020

机译：临床癌症试验中的超敏反不良事件报告：障碍和潜在的解决方案，用于研究人口水平的严重事件
6. Patient free text reporting of symptomatic adverse events in cancer clinical research using the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) [O] . Arlene E Chung, Kimberly Shoenbill, Sandra A Mitchell, 2019

机译：使用美国国家癌症研究所的患者报告的不良事件通用术语标准（PRO-CTCAE）版本免费报告患者在癌症临床研究中有症状的不良事件的文本
7. Patient free text reporting of symptomatic adverse events in cancer clinical research using the National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) [O] . Arlene E Chung, Kimberly Shoenbill, Sandra A Mitchell, 2019

机译：患者自由文本报告癌症临床研究中的症状不良事件使用国家癌症研究所的患者报告的不良事件的常见术语标准（Pro-CTCAE）的常见术语标准
8. Adverse Events and Their Association with Treatment Regimens in the DiabetesControl and Complications Trial (DCCT). Analysis Documentation [R] . 1996

机译：不良事件及其与糖尿病控制和并发症试验（DCCT）中治疗方案的关联。分析文档

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