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The Clinical Study of Multi-level Systemic Strategy based on Molecular Targeting and Immunochemotherapy for AIDS-related Highly Aggressive B-cell Lymphoma

The Clinical Study of Multi-level Systemic Strategy based on Molecular Targeting and Immunochemotherapy for AIDS-related Highly Aggressive B-cell Lymphoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035526
Enrollment
Unknown
Registered
2020-08-13
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

AIDS-related Highly Aggressive B-cell Lymphoma

Interventions

Case series:immunochemotherapy and molecular targeted therapy

Sponsors

Shanghai Public Health Clinical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed and relapsed/refractory AIDS-related highly aggressive B-cell lymphoma; 2. Aged 18-70 years, male or female; 3. Non-pregnant and lactating women; 4. For all women of childbearing age, hCG must be measured by pregnancy test to exclude pregnancy status; 5. For all men of childbearing age, contraception must be used during treatment until 3 months after withdrawal of the drug; 6. Signed Informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Allergies or contraindications to any of the drugs covered by the protocol; 2. Liver and renal function: serum bilirubin >35 umol/L, AST/ALT below two times the upper limit of normal, serum creatinine >150 umol/L; 3. Cardiac disease: including echocardiographic EF 2), electrocardiographic QTc > 470 ms; 4. Pulmonary disease: pulmonary edema, pleural effusion (CTCAE score > 2); 5. Combined with other malignant tumors; 6. Patients with active HAV, HBV, HCV and tuberculosis; 7. Inability to understand or comply with research protocols; 8. Concurrent participation in other clinical investigators; 9. Other conditions that the researchers considered inappropriate for inclusion.

Design outcomes

Primary

MeasureTime frame
overall surviral rate;Progression-free survival rate;

Countries

China

Contacts

Public ContactRenfang Zhang

Shanghai Public Health Clinical Center

zhangrenfang@shphc.org.cn+86 021-37990333-3223

Outcome results

None listed

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