How to take Rituximab

Rituximab (Rituximab) is a prescription drug that is infused into a vein in the form of a solution (liquid). Its use must be carried out by doctors and medical staff. For adults, the first dose should be infused at a rate of 50mg/hr. In the absence of infusion toxicity, increase the infusion rate in 50 mg/hr increments every 30 minutes to a maximum of 400 mg/hr. In pediatric patients, the infusion can be initiated at a rate of 0.5 mg/kg/hr (maximum 50 mg/hr). In the absence of infusion toxicity, increase the infusion rate by 0.5 mg/kg/hr every 30 minutes to a maximum of 400 mg/hr. Subsequent infusions are initiated at a rate of 100 mg/hr and, in the absence of infusion toxicity, increase the rate in 100 mg/hr increments at 30-minute intervals to a maximum of 400 mg/hr.

1. Recommended dose for non-Hodgkin lymphoma (NHL): The recommended dose is 375mg/m2.

(1)Patients with relapsed or refractory, low-grade or follicular, CD20-positive, B-cell non-Hodgkin lymphoma take 4 or 8 doses once a week.

(2)Patients with relapsed or refractory, low-grade or follicular, CD20-positive B-cell non-Hodgkin lymphoma undergoing treatment once weekly for a total of 4 doses.

(3)Patients with previously untreated follicularCD20-positive B-cell non-Hodgkin lymphoma given on day 1 of each chemotherapy cycle, up to 8 doses. For patients in complete or partial response, eight weeks after completing combination therapy with a rituximab product and chemotherapy, rituximab maintenance therapy is initiated every every 8 weeks for a total of 12 doses.

(4)First-line Patients with non-progressive, low-grade, CD20-positive B-cell non-Hodgkin lymphoma after completing 6-8 cycles of CVP chemotherapy, 4 doses each time, 6 months apart, up to 16 doses.

(5)Patients with diffuse largeB-cell non-Hodgkin lymphoma given on Day 1 of each chemotherapy cycle, up to 8 infusions.

(6) Pediatric patients are using rituximab in combination with chemotherapy. The treatment includes 2 induction phases and 2 consolidation phases, with a total of 6 administrations. In each induction period, the recommended dose is 375 mg/m2, administered by intravenous infusion, on the second or first day of chemotherapy, for a total of 2 doses; the drug is administered once every 48 hours. In each consolidation period, the recommended dose is 375 mg/m2, administered by intravenous infusion, and administered on the first day of chemotherapy.

2. Recommended dose for chronic lymphocytic leukemia (CLL):

StartThe recommended dose of FC chemotherapy is 375mg/m2 the day before, then 500mg/m2 on day 1 of cycles 2-6 (every 28 days).

3. Recommended dose of Zevalin component for the treatment of non-Hodgkin lymphoma: When used as part of Zevalin treatment regimen, infuse 250 mg/m2.

4. Rheumatoid arthritis (RA):

Intravenous infusion of rituximab in two doses, each time1000mg, 2 weeks apart. It is recommended that 100 mg of methylprednisolone or a corticosteroid equivalent be given intravenously 30 minutes before each infusion to reduce the incidence and severity of infusion-related reactions. Subsequent courses of treatment should be performed every 24 weeks or based on clinical assessment, but no earlier than every 16 weeks. Rituximab is used in combination with methotrexate.

5. Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA):

(1) Induction therapy for adult patients with active GPA/MPA:

Intravenous infusion of rituximab375 mg/m2 once weekly for 4 weeks. According to clinical practice, 1000 mg of methylprednisolone is administered intravenously every day for 1 to 3 days, followed by oral prednisone. This regimen should be initiated within 14 days before or after starting rituximab and may be continued during and after the 4-week induction period of rituximab treatment.

(2) Follow-up treatment of GPA/MPA:

Rituximab is administered as two intravenous infusions of 500 mg each time, two weeks apart, followed by 500 mg intravenous infusions every 6 months based on clinical assessment. If a rituximab product is used for induction therapy of active disease, initiate subsequent treatment with rituximab within 24 weeks after the last induction infusion with the rituximab product or based on clinical assessment, but no earlier than 16 weeks after the last induction infusion with the rituximab product. If other standard immunosuppressants were used for induction therapy in active disease, initiate follow-up treatment with rituximab within 4 weeks after disease control.

(3) Induction therapy for children with active GPA/MPA:

Intravenous infusion of rituximab375 mg/m2 once weekly for 4 weeks. Prior to the first infusion of rituximab, give methylprednisolone 30 mg/kg (not to exceed 1 g/day) intravenously once daily for 3 days. After intravenous methylprednisolone, oral steroids should be continued according to clinical practice.

(4) Follow-up treatment for children with GPA/MPA:

Rituximab is given as an intravenous infusion of 250 mg/m2 in two divided doses, two weeks apart, followed by an intravenous infusion of 250 mg/m2 every 6 months based on clinical assessment. If a rituximab product is used for induction therapy of active disease, initiate subsequent treatment with rituximab within 24 weeks after the last induction infusion with the rituximab product or based on clinical assessment, but no earlier than 16 weeks after the last induction infusion with the rituximab product.

6. Pemphigus vulgaris (PV):

Rituximab is given as an intravenous infusion of 1000 mg in two divided doses, 2 weeks apart, and combined with a decreasing course of glucocorticoids. Intravenous infusion of rituximab 500 mg for maintenance treatment at month 12 and every 6 months thereafter or based on clinical assessment. At the time of relapse, 1000 mg of rituximab was administered intravenously, and the glucocorticoid dose was considered to be resumed or increased based on clinical assessment. Subsequent infusions can be given up to 16 weeks after the previous infusion.