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Proteome and metaborome analyses for drug response in cancer patients with solid tumor receiving chemotherapy

Proteome and metaborome analyses for drug response in cancer patients with solid tumor receiving chemotherapy - Proteome and metaborome analyses in drug response for cancer chemotherapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001356
Enrollment
50
Registered
2008-09-04
Start date
2008-09-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Cancer

Interventions

genome, pharmacokinetics, proteome and metaborome

Sponsors

Saitama Medical University, International Medical Center, Department of Medical Oncology
Lead Sponsor
Showa University, School of Medicine, Division of Respiratory and Allergy Department of Internal Medicine Keio University, School of Medicine, Department of Pharmacy
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients with histologically confirmed solid tumors. 2)Patients who are 20 years or higher. 3)Patients with ECOG performance status of 0 to 3. 4)Patients who are expected to live at least 2 months or more. 5)Patients with measurable and evaluable lesion(s). 6)Patients never treated with the target anticancer drug(s). No history of chemotherapy or within 3 weeks. 7)Blood tests 1. Neutrophile count 2000 /mm3 or higher. 2. Platelet count 100,000 /mm3 or higher. 3. Hemoglobin 9.0 g/dL or higher. 4. AST, ALT less than 2.0 times the upper limit of normal. 5. Total bilirubin 2.0 mg/dL or less. 6. Serum creatinine 1.5 mg/dLor less. 8)All patients were asked for written informed consent for their peripheral blood samples and medical information to be used for research purposes.

Exclusion criteria

Exclusion criteria: 1)Patients with interstitial pneumonia or pulmonary fibrosis. 2)Patients with severe infection (with fever). 3)Patients with incontrollable diabetes. 4)Patients with severe heart failure. 5)Patients with severe complication such as cirrhosis. 6)Patients with mental or nerve disorder. 7)Pregnant patients or patients giving the breast. Men and wemen who want to make baby. 8)Patients with severe allergy or those who had severe allergy in the past. 9)Patients who are contraindication for cancer chamotherapy. 10)Patients hypersensitive to the anticancer drug(s). 11)Patients who are not appropriate to participate in the study safely.

Design outcomes

Primary

MeasureTime frame
Genetic polymorphisms in factors associated with pharmacokinetics and pharmacodynamics of anticancer drugs, proteome and metaborome, anticancer effects and adverse drug reactions.

Countries

Japan

Contacts

Public ContactYasutsuna Sasaki

Saitama Medical University, International Medical Center Medical Oncology

ysasaki@saitama-med.ac.jp042-984-4679

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026