Gastrointestinal malignant tumor, Breast cancer
Conditions
Interventions
None listed
Sponsors
Saitama Medical Center Saitama Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Adequate organ functiont 2.Psrformance status:0-2 3.Written informed consent prior to sutudy-spe cific screening procedure
Exclusion criteria
Exclusion criteria: Cannot collect saliva by oneself.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| At the time of the intravenous feeding dosage end of the anticancer agent, We collect saliva seven days later for 72 hours for 24 hours. We measure the drug blood concentration of saliva which we collected qualitatively and quantitatively using liquid chromatograph - tandem type mass spectrometer (LC/MS/MS). | — |
Countries
Japan
Contacts
Public ContactMotohiko Sano
Saitama Medical Center Saitama Medical University department of pharmacy
Outcome results
None listed