Cancer patient who will receive chemotherapy
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Cancer patient who will recieve chemotherapy 2) Age over 1 year 3) Samples meeting one of the followings: 3)-1Tumor tissue i) Surplus sample stored in the NCC biobank ii) Surplus sample of diagnostic biopsy iii) Surgical surplus tumor sample iv) Newly-taken tumor sample for this study 3)-2 Non-tumor tissue i) Surplus tissue and blood in the NCC biobank ii) Newly-taken blood (5-20mL) for this study iii) Newly-taken oral mucosa for this study iv) Newly-taken non-tumor gastrointestinal mucosa for this study 4) Written informed consent
Exclusion criteria
Exclusion criteria: 1) Judged ineligible by the clinical investigators
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analysis of somatic gene mutation, gene expression of tumor tissue | — |
Secondary
| Measure | Time frame |
|---|---|
| Polymorphism analysis of genes related to the pharmacodynamics and pharmacokinetics in non-tumor tissue | — |
Countries
Japan
Contacts
National Cancer Center Hospital Department of Experimental Therapeutics