跳至主要内容
临床试验/NCT02458040
NCT02458040撤回不适用

Clinical Benefit of Genetic Biomarkers for Guiding Treatment Decisions in Oncology Drugs

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家开始时间: 2015年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Overall Survival (OS)

研究概览

简要总结

This study is a meta-epidemiological study which aim is to quantify the clinical benefit of the biomarker-based strategy compared to conventional strategy across all drugs with such a strategy.

详细描述

Personalized medicine consist to differentially treat patients based on their individual characteristics (mainly genetics). It is of the most promising area of cancer research and cancer care. The label of more than 140 FDA- approved drugs mention a biomarker, the majority being indicated in oncology. However, it has also been suggested that the hopes of personalized medicine were not matched by evidence. Indeed, there is a threat that genetic biomarkers are used without evidence that this use translates in improved outcomes for patients, and the use of biomarkers is in need for thorough validation.

In a previous work the investigators showed that the mention of a pharmacogenomic biomarker in a drug label can have different meanings depending on the drug, and that oncology had higher proportion of required or recommended genetic testing compared to other therapeutic areas. Hence, the investigators will include only the drug-biomarker pairs with (i) required or recommended genetic testing, or (ii) with biomarker-based indication and (iii) with at least one indication in oncology.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

性别
All
接受健康志愿者

入选标准

  • phase II or III randomized clinical trials
  • including patients with one of the drug-biomarker-indication triplet studied
  • evaluating treatment effect in biomarker-defined strata (either in biomarker-positive patients, in biomarker-negative patients or in both strata).
  • reporting OS or PFS or DFS

排除标准

  • 未提供

研究组 & 干预措施

Biomarker-positive patients

干预措施: Drug selected in the study (Drug)

Biomarker-negative patients

干预措施: Drug selected in the study (Drug)

All patients

干预措施: Drug selected in the study (Drug)

结局指标

主要结局

Overall Survival (OS)

时间窗: Up to 5 years

次要结局

  • Progression-Free Survival (PFS)(Up to 5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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