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Radioimmunotherapy with 177Lu-DOTA-RITUXIMAB in B-cell lymphoma

The efficacy of radioimmunotherapy with 177Lu-DOTA-RITUXIMAB in refractory or relapsing follicular, mantle cell, and other indolent B-cell lymphomas

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210612051548N4
Enrollment
10
Registered
2021-11-28
Start date
2021-12-22
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

CD20-positive B-cell Lymphoma. Small cell B-cell lymphoma

Interventions

Intervention group: Intervention group: In this study, the 177Lu-DOTA-RITUXIMAB PET/CT radiopharmaceutical will be injected intravenously into 10 patients with lymphoma according to the 18F-FDG PET/CT

Sponsors

Boushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Histologically confirmed relapsed or refractory CD20-positive B-cell lymphoma Age greater than 18 years Life expectancy more than 3 months Notpregnant or lactating women Performance status of 2 or better according to the World Health Organization scale. Absolute neutrophil count above1.5 × 109/L, a circulating lymphocyte count below 5 × 109/L, a platelet count above 100 · 109/L, a total bilirubin level of no more than 20 mmol/L, an alanine aminotransferase level below 2.5 times normal, and a serum creatinine clearance level above 60 mL/min. Signed informed consent form

Exclusion criteria

Exclusion criteria: Patients who had previously undergone radiation therapy to the pelvis, femora, or lumbar spine or high-dose treatment with stem cell transplantation.

Design outcomes

Primary

MeasureTime frame
Number of patients with toxicity. Timepoint: weekly up to week 10 or until recovery from nadir. Method of measurement: Blood chemistry, hematology, and urine analysis.;The proportion of patients who have a partial, stable (not-progressed), or complete response to therapy. Timepoint: 8-12 weeks after treatment. Method of measurement: 18F-FDG PET/CT.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Assadi

Boushehr University of Medical Sciences

assadipoya@yahoo.com+98 77 3332 0361

Outcome results

None listed

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