Clinical Pharmacology, Pharmaceutical Sciences, Pharma Research and Early Development (pRED), Roche Innovation Center, New York, 430 East 29th Street, 10016, New York City, NY, USA.
Global Product Development, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
Cancer Chemother Pharmacol. 2019 Sep;84(3):661-666. doi: 10.1007/s00280-019-03818-1. Epub 2019 Mar 21.
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.
利妥昔单抗是大多数 B 细胞恶性肿瘤的标准治疗方法。它的快速临床开发使患者能够更早地接受这种延长生命的药物;然而,这也排除了对剂量选择的彻底评估。从最近的皮下开发项目中收集的广泛临床药理学数据使人们能够重新审视这个老问题,并支持在大多数患者中,批准的利妥昔单抗在非霍奇金淋巴瘤和慢性淋巴细胞白血病中的剂量方案似乎最大限度地提高了临床获益。