Abstract
Rituximab is the standard of care for most B-cell malignancies. Its rapid clinical development enabled patients to receive this life-prolonging medicine sooner; however, it precluded a thorough assessment of dose selection. Extensive clinical pharmacology data collected from the recent subcutaneous development program enabled re-examination of this old question and support that the approved rituximab dosing regimens in non-Hodgkin’s lymphoma and chronic lymphocytic leukemia appear to maximize the clinical benefit in the majority of patients.
| Original language | English |
|---|---|
| Pages (from-to) | 661-666 |
| Number of pages | 6 |
| Journal | Cancer Chemotherapy and Pharmacology |
| Volume | 84 |
| Issue number | 3 |
| DOIs | |
| State | Published - Sep 1 2019 |
Keywords
- Dose selection
- Exposure–response
- Monoclonal antibody
- Rituximab
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