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Precision Medicine Study about Drug Effect and Adverse Reaction of Rituximab in lymphonma Treatment Based on Metabonomics, Pharmacogenomics and Gut Microbiota.

Precision Medicine Study about Drug Effect and Adverse Reaction of Rituximab in lymphonma Treatment Based on Metabonomics, Pharmacogenomics and Gut Microbiota.

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017001
Enrollment
Unknown
Registered
2018-07-07
Start date
2018-07-16
Completion date
Unknown
Last updated
2019-11-11

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

Conditions

B cell lymphoma

Interventions

Case series:none

Sponsors

Sun Yat-Sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. patients diagnosed as CD20 (+) B-cell lymphoma and received rituximab; 2. patients who had not been treated with chemotherapy or radiotherapy before, or more than 3 years after the last treatment of rituximab; 3. Imaging at least one measurable lesion; 4. patients aged from 16 to 80 years; 5. life expectancy greater than 12 weeks; 6. adequate organ function, Bone marrow reserve: hemoglobin = 9.0 g/dL, white blood cell = 3000/µL, neutrophil absolute value = 1500/µL, platelet = 100000/µL; renal function (serum creatinine = 1.5 mg / dL, creatinine clearance = 50 mL/min); upper limit of liver function (normal value of total bilirubin = 2 times), The upper limit of the normal value of alanine aminotransferase = 3 times), the normal electrocardiogram, the myocardial ejection fraction = 50.

Exclusion criteria

Exclusion criteria: 1. all kinds of congenital or acquired immunodeficiency patients, such as: AIDSN Wiskott-Aldrich syndrome, hereditary ataxia-telangiectasia, liver/kidney transplantation patients who nedd long-term oral anti-rejection drugs and other immunodeficiency patients; 2. Secondary lymphoma developed after chemotherapy or radiotherapy for other malignant tumors; 3. Patients with active infections requiring systemic antibiotic or antiviral therapy; 4. Patients with decompensated heart failure, dilated cardiomyopathy, St segment depression coronary heart disease or experienced myocardial infarction in the last 6 months; 5. Patients with severe mental illness; lactation or pregnancy women.

Design outcomes

Primary

MeasureTime frame
objective response;

Secondary

MeasureTime frame
Progression free survival;adverse events;

Countries

China

Contacts

Public ContactWang Xueding
rongshu_zlyy@126.com+86 02087433323

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026