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

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

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02458040
Enrollment
0
Registered
2015-05-29
Start date
2015-05-31
Completion date
2016-12-31
Last updated
2023-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasms

Brief summary

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.

Detailed description

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.

Interventions

DRUGDrug selected in the study

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frame
Overall Survival (OS)Up to 5 years

Secondary

MeasureTime frame
Progression-Free Survival (PFS)Up to 5 years

Other

MeasureTime frame
Disease-Free Survival (DFS)Up to 5 years

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026