cancer malignancies
Conditions
Interventions
None listed
Sponsors
Antoni van Leeuwenhoek Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patients using a (currently approved or new) targeted anti-cancer agent for treatment of cancer Patients from whom it is possible to collect blood samples Informed consent is given
Exclusion criteria
Exclusion criteria: nvt
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| •Pharmacokinetics | — |
Secondary
| Measure | Time frame |
|---|---|
| •Treatment outcome (response, suboptimal response, treatment failure) •Toxicity (graded on basis of the National Cancer Institute Common Toxicity Terminology grading Criteria for adverse events (CTCAE) •Genotype of drug metabolising enzymes and drug transporters •Mutations and/or alterations in drug targets •Drug-drug interactions | — |
Countries
Netherlands
Outcome results
None listed