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» Home » CAD » Oncology » Hematology » B-Cell lymphoma
Background
Epidemiology
Anatomy
Pathophysiology
Etiology
Genetics
Prognostic Factors
Clinical History
Physical Examination
Age group
Associated comorbidity
Associated activity
Acuity of presentation
Differential Diagnoses
Laboratory Studies
Imaging Studies
Procedures
Histologic Findings
Staging
Treatment Paradigm
by Stage
by Modality
Chemotherapy
Radiation Therapy
Surgical Interventions
Hormone Therapy
Immunotherapy
Hyperthermia
Photodynamic Therapy
Stem Cell Transplant
Targeted Therapy
Palliative Care
Medication
Each cycle is 28 days
(Cycle 1)
At the beginning of the treatment, a step-up dose of 0.16 mg administered subcutaneously (SC) was given on the first day
On the eighth day, another step-up dose of 0.8 mg SC was given as a single dose
On the fifteenth day, the patient received a full dose of 48 mg SC in a single administration, requiring hospitalization for 24 hours during the initial 48-mg dose
On the twenty-second day, a single dose of 48 mg SC was administered
(Cycles 2 & 3)
Administer a single subcutaneous dose of 48 mg on days 1, 8, 15, and 22
(Cycles 4 to 9)
On Days 1 and 15, a single dose of 48 mg should be administered subcutaneously
(Cycle 10 & after that)
On the first day, administer a single subcutaneous dose of 48 mg
Indicated for B-Cell Lymphoma
Step up dose regimen:
Dosing starts with step up dose regimen, administer premedication for every dose
1-Cycle:
Day-1: After completion of the obinutuzumab dose, administer glofitamab as intravenous infusion
Day-8: glofitamab 2.5 mg intravenous over 4 hours for one time (step up dose-1)
Day-15: glofitamab 10 mg intravenous over 4 hours for one time (step up dose-2)
If a patient ever experienced CRS with an earlier dose, prolong the infusion rate for over 8 hours
2-Cycle:
Day-1: glofitamab 30 mg intravenous over 4 hours
If a patient ever experienced CRS with an earlier dose, prolong the infusion rate for over 8 hours
3-12 Cycle:
Day-1: glofitamab 30 mg intravenous over 4 hours
If a patient ever experienced CRS with an earlier dose, maintain the time of infusion at 4 hours
Continue the therapy for a maximum of 12 cycles, which includes the initial step-up dosing in 1-Cycle; or until there is disease progression or if unacceptable toxicity arises, whichever comes first
400
mg/kg/dose
Intravenous (IV)
daily
3 - 4
weeks
Future Trends
References
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» Home » CAD » Oncology » Hematology » B-Cell lymphoma
Each cycle is 28 days
(Cycle 1)
At the beginning of the treatment, a step-up dose of 0.16 mg administered subcutaneously (SC) was given on the first day
On the eighth day, another step-up dose of 0.8 mg SC was given as a single dose
On the fifteenth day, the patient received a full dose of 48 mg SC in a single administration, requiring hospitalization for 24 hours during the initial 48-mg dose
On the twenty-second day, a single dose of 48 mg SC was administered
(Cycles 2 & 3)
Administer a single subcutaneous dose of 48 mg on days 1, 8, 15, and 22
(Cycles 4 to 9)
On Days 1 and 15, a single dose of 48 mg should be administered subcutaneously
(Cycle 10 & after that)
On the first day, administer a single subcutaneous dose of 48 mg
Indicated for B-Cell Lymphoma
Step up dose regimen:
Dosing starts with step up dose regimen, administer premedication for every dose
1-Cycle:
Day-1: After completion of the obinutuzumab dose, administer glofitamab as intravenous infusion
Day-8: glofitamab 2.5 mg intravenous over 4 hours for one time (step up dose-1)
Day-15: glofitamab 10 mg intravenous over 4 hours for one time (step up dose-2)
If a patient ever experienced CRS with an earlier dose, prolong the infusion rate for over 8 hours
2-Cycle:
Day-1: glofitamab 30 mg intravenous over 4 hours
If a patient ever experienced CRS with an earlier dose, prolong the infusion rate for over 8 hours
3-12 Cycle:
Day-1: glofitamab 30 mg intravenous over 4 hours
If a patient ever experienced CRS with an earlier dose, maintain the time of infusion at 4 hours
Continue the therapy for a maximum of 12 cycles, which includes the initial step-up dosing in 1-Cycle; or until there is disease progression or if unacceptable toxicity arises, whichever comes first
400
mg/kg/dose
Intravenous (IV)
daily
3 - 4
weeks
same as adult dosing
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